Integrative genomics viewer (scientific article (publication date: 2011))

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Q34471717	Adaptive evolution and the birth of CTCF binding sites in the Drosophila genome
Q55225078	Adaptive modulation of antibiotic resistance through intragenomic coevolution.
Q54266417	Adar3 Is Involved in Learning and Memory in Mice.
Q90737911	Added Value of Clinical Sequencing: WGS-Based Profiling of Pharmacogenes
Q49979102	Addition of m6A to SV40 late mRNAs enhances viral structural gene expression and replication.
Q54210521	Adeno-associated Virus Genome Population Sequencing Achieves Full Vector Genome Resolution and Reveals Human-Vector Chimeras.
Q41434819	Adult-onset obesity is triggered by impaired mitochondrial gene expression.
Q39473847	Advances in finding Alba: the locus affecting life history and color polymorphism in a Colias butterfly.
Q98564393	Advancing brain barriers RNA sequencing: guidelines from experimental design to publication
Q35830949	Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma.
Q60920695	Allele Frequencies in Depressed Patients of European Descent in Russia
Q37396878	Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta
Q36068276	Allele-Specific Transcriptome and Methylome Analysis Reveals Stable Inheritance and Cis-Regulation of DNA Methylation in Nasonia
Q64388679	Allele-specific genome editing using CRISPR-Cas9 is associated with loss of heterozygosity in diploid yeast
Q37369276	Allelic barley MLA immune receptors recognize sequence-unrelated avirulence effectors of the powdery mildew pathogen
Q35863035	Allelic ratios and the mutational landscape reveal biologically significant heterozygous SNVs
Q31140278	Almendravirus: A Proposed New Genus of Rhabdoviruses Isolated from Mosquitoes in Tropical Regions of the Americas
Q89881693	Alterations in chromatin at antigen receptor loci define lineage progression during B lymphopoiesis
Q90436002	Alterations in the methylome of the stromal tumour microenvironment signal the presence and severity of prostate cancer
Q102319892	Alterations of 5-hydroxymethylcytosines in circulating cell-free DNA reflect retinopathy in type 2 diabetes
Q42374319	Alterations of c-di-GMP turnover proteins modulate semi-constitutive rdar biofilm formation in commensal and uropathogenic Escherichia coli.
Q90464649	Altered secretory and neuroprotective function of the choroid plexus in progressive multiple sclerosis
Q37501768	Alternate-locus aware variant calling in whole genome sequencing
Q90702145	Alternative Splicing Detection Tool-a novel PERL algorithm for sensitive detection of splicing events, based on next-generation sequencing data analysis
Q36217564	Alternative Splicing within and between Drosophila Species, Sexes, Tissues, and Developmental Stages
Q37213678	Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution.
Q36726792	Alternative transcription initiation leads to expression of a novel ALK isoform in cancer
Q36380694	Alu element-containing RNAs maintain nucleolar structure and function
Q61964007	Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias
Q26785310	Alview: Portable Software for Viewing Sequence Reads in BAM Formatted Files
Q30833465	AmalgamScope: merging annotations data across the human genome.
Q42774446	Ammonium induces differential expression of methane and nitrogen metabolism-related genes in Methylocystis sp. strain SC2.
Q34945003	Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
Q64077492	An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease
Q92074504	An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome
Q92824007	An ATR and CHK1 kinase signaling mechanism that limits origin firing during unperturbed DNA replication
Q24310429	An AUTS2-Polycomb complex activates gene expression in the CNS.
Q40071151	An Ago2-associated capped transcriptional start site small RNA suppressing adenovirus DNA replication.
Q92536533	An Allosteric Network for Spliceosome Activation Revealed by High-Throughput Suppressor Analysis in Saccharomyces cerevisiae
Q35932166	An Association Rule Mining Approach to Discover lncRNAs Expression Patterns in Cancer Datasets
Q91578150	An Essential Regulator of Bacterial Division Links FtsZ to Cell Wall Synthase Activation
Q35810825	An Exon-Capture System for the Entire Class Ophiuroidea
Q47167605	An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS.
Q35781738	An Interaction between RRP6 and SU(VAR)3-9 Targets RRP6 to Heterochromatin and Contributes to Heterochromatin Maintenance in Drosophila melanogaster
Q40200877	An Introduction to Genome Annotation
Q27346955	An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed
Q92214286	An LKB1-SIK Axis Suppresses Lung Tumor Growth and Controls Differentiation
Q56341789	An Promoter-Trap: Augmenting Genome Annotation and Functional Genomics
Q46669728	An RNA-based approach to sequence the mitogenome of Hypoptopoma incognitum (Siluriformes: Loricariidae).
Q90713381	An RNA-seq based comparative approach reveals the transcriptome-wide interplay between 3'-to-5' exoRNases and RNase Y
Q34044471	An Updated Collection of Sequence Barcoded Temperature-Sensitive Alleles of Yeast Essential Genes
Q28298001	An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1
Q42621989	An aberrant transcription factor network essential for Wnt signaling and stem cell maintenance in glioblastoma.
Q92147149	An accessible GenePattern notebook for the copy number variation analysis of Illumina Infinium DNA methylation arrays
Q42055024	An active immune defense with a minimal CRISPR (clustered regularly interspaced short palindromic repeats) RNA and without the Cas6 protein
Q41125131	An efficient method for genome-wide polyadenylation site mapping and RNA quantification
Q100512260	An embryonic stem cell-specific heterochromatin state promotes core histone exchange in the absence of DNA accessibility
Q58130461	An environmental DNA sampling method for aye-ayes from their feeding traces
Q37628805	An evaluation of high-throughput approaches to QTL mapping in Saccharomyces cerevisiae
Q53303389	An evolutionary metabolic engineering approach for enhancing lipogenesis in Yarrowia lipolytica.
Q101121024	An extreme-phenotype genome-wide association study identifies candidate cannabinoid pathway genes in Cannabis
Q38692859	An immunogenic personal neoantigen vaccine for patients with melanoma
Q58129932	An improved approach for reconstructing consensus repeats from short sequence reads
Q30887413	An integrated approach for analyzing clinical genomic variant data from next-generation sequencing.
Q54976470	An integrated global regulatory network of hematopoietic precursor cell self-renewal and differentiation.
Q99572035	An integrated personal and population-based Egyptian genome reference
Q33728558	An integrative analysis reveals functional targets of GATA6 transcriptional regulation in gastric cancer.
Q64891192	An integrative approach identifies direct targets of the late viral transcription complex and an expanded promoter recognition motif in Kaposi's sarcoma-associated herpesvirus.
Q47398821	An integrative strategy to identify the entire protein coding potential of prokaryotic genomes by proteogenomics.
Q42289714	An interaction network of mental disorder proteins in neural stem cells
Q35939573	An interactive environment for agile analysis and visualization of ChIP-sequencing data
Q35113174	An interspecific fungal hybrid reveals cross-kingdom rules for allopolyploid gene expression patterns
Q91739794	An intestinal zinc sensor regulates food intake and developmental growth
Q52339755	An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease.
Q53835008	An optimized FAIRE procedure for low cell numbers in yeast.
Q97424216	An organoid-based drug screening identified a menin-MLL inhibitor for endometrial cancer through regulating the HIF pathway
Q30567093	Analysing and interpreting DNA methylation data
Q34812858	Analysis and annotation of the hexaploid oat seed transcriptome
Q35884709	Analysis of DNA Methylation and Hydroxymethylation in the Genome of Crustacean Daphnia pulex
Q112716011	Analysis of Genomic DNA from Medieval Plague Victims Suggests Long-Term Effect of Yersinia pestis on Human Immunity Genes
Q54970332	Analysis of LCT-13910 genotypes and bone mineral density in ancient skeletal materials.
Q93166280	Analysis of Mammalian Native Elongating Transcript sequencing (mNET-seq) high-throughput data
Q36132301	Analysis of Polygenic Mutants Suggests a Role for Mediator in Regulating Transcriptional Activation Distance in Saccharomyces cerevisiae
Q64446568	Analysis of RNA-Seq datasets reveals enrichment of tissue-specific splice variants for nuclear envelope proteins
Q41601457	Analysis of RNAseq datasets from a comparative infectious disease zebrafish model using GeneTiles bioinformatics
Q33352695	Analysis of cancer metabolism with high-throughput technologies
Q33910961	Analysis of copy number variation in the Abp gene regions of two house mouse subspecies suggests divergence during the gene family expansions
Q54988618	Analysis of human ES cell differentiation establishes that the dominant isoforms of the lncRNAs RMST and FIRRE are circular.
Q91405217	Analysis of mRNA processing at whole transcriptome level, transcriptomic profile and genome sequence refinement of Trypanosoma cruzi
Q27468729	Analysis of the Langat Virus Genome in Persistent Infection of an Ixodes scapularis Cell Line
Q95841099	Analysis of the Mouse Y Chromosome by Single-Molecule Sequencing With Y Chromosome Enrichment
Q43684053	Analysis of the canine brain transcriptome with an emphasis on the hypothalamus and cerebral cortex.
Q61443851	Analysis of the human Y-chromosome haplogroup Q characterizes ancient population movements in Eurasia and the Americas
Q37519903	Analysis of the mRNA targetome of microRNAs expressed by Marek's disease virus
Q24596120	Analysis of the small RNA transcriptional response in multidrug-resistant Staphylococcus aureus after antimicrobial exposure
Q47439995	Analytical Validation of the Next-Generation Sequencing Assay for a Nationwide Signal-Finding Clinical Trial: Molecular Analysis for Therapy Choice Clinical Trial
Q34670822	Analytical tools and current challenges in the modern era of neuroepigenomics
Q41071560	Anatomical distribution of Mycobacterium bovis genotypes in experimentally infected white-tailed deer
Q42773819	Ancestral Y-linked genes were maintained by translocation to the X and Y chromosomes fused to an autosomal pair in the Okinawa spiny rat Tokudaia muenninki
Q36984439	Anchored pseudo-de novo assembly of human genomes identifies extensive sequence variation from unmapped sequence reads
Q57094474	Ancient DNA reveals the chronology of walrus ivory trade from Norse Greenland
Q47552600	Ancient Human Migrations to and through Jammu Kashmir- India were not of Males Exclusively.
Q64107568	Ancient Mitochondrial Genomes Reveal the Absence of Maternal Kinship in the Burials of Çatalhöyük People and Their Genetic Affinities
Q38735381	Androgen receptor uses relaxed response element stringency for selective chromatin binding and transcriptional regulation in vivo.
Q36665483	Aneuploidy shortens replicative lifespan in Saccharomyces cerevisiae
Q34031604	Angiomyolipoma have common mutations in TSC2 but no other common genetic events
Q41384442	Annotated Draft Genome Assemblies for the Northern Bobwhite (Colinus virginianus) and the Scaled Quail (Callipepla squamata) Reveal Disparate Estimates of Modern Genome Diversity and Historic Effective Population Size
Q35672877	Annotation of the Protein Coding Regions of the Equine Genome
Q93055803	Antibiotic production in Streptomyces is organized by a division of labor through terminal genomic differentiation
Q99248337	Antibiotic susceptibility signatures identify potential antimicrobial targets in the Acinetobacter baumannii cell envelope
Q37461459	Antisense transcription licenses nascent transcripts to mediate transcriptional gene silencing
Q37123047	Apolipoprotein L1 Variant Associated with Increased Susceptibility to Trypanosome Infection
Q36086105	Application of Circulating Tumor DNA as a Non-Invasive Tool for Monitoring the Progression of Colorectal Cancer
Q35135586	Application of Next Generation Sequencing for personalized medicine for sudden cardiac death
Q42172387	Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state.
Q34603432	Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment
Q49209858	Application of next‑generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss.
Q39324061	Application of recombinant TAF3 PHD domain instead of anti-H3K4me3 antibody.
Q36855805	Application of single-cell RNA sequencing in optimizing a combinatorial therapeutic strategy in metastatic renal cell carcinoma.
Q47738170	Applying Precision Medicine to Ovarian Cancer: Proof-of-Principle for a "Molecular Second Look".
Q92040652	Approaches to study CRISPR RNA biogenesis and the key players involved
Q92262712	Archaic mitochondrial DNA inserts in modern day nuclear genomes
Q38881648	Argonaute 2 Binds Directly to tRNA Genes and Promotes Gene Repression in cis.
Q52639371	Array-based DNA-methylation profiling in sarcomas with small blue round cell histology provides valuable diagnostic information.
Q28256153	Artemis: an integrated platform for visualization and analysis of high-throughput sequence-based experimental data
Q40394314	Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications.
Q64250262	Artificial MicroRNAs Targeting C9orf72 Can Reduce Accumulation of Intra-nuclear Transcripts in ALS and FTD Patients
Q89831611	Ascl2-Dependent Cell Dedifferentiation Drives Regeneration of Ablated Intestinal Stem Cells
Q60950339	Assaying RNA structure with LASER-Seq
Q31130984	Assembly of the Complete Sitka Spruce Chloroplast Genome Using 10X Genomics' GemCode Sequencing Data.
Q91335030	Assessing inter-component heterogeneity of biphasic uterine carcinosarcomas
Q96231871	Assessing the Performance of Dried-Blood-Spot DNA Extraction Methods in Next Generation Sequencing
Q35643228	Assessing the genetic variation of Ty-1 and Ty-3 alleles conferring resistance to tomato yellow leaf curl virus in a broad tomato germplasm.
Q42718507	Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory.
Q92860560	Assessment of low-coverage nanopore long read sequencing for SNP genotyping in doubled haploid canola (Brassica napus L.).
Q47208649	Assessment of piRNA biogenesis and function in testicular germ cell tumors and their precursor germ cell neoplasia in situ
Q57052739	Assessment of shared alleles in drought-associated candidate genes among southern California white oak species (Quercus sect. Quercus)
Q61447370	Assessment of somatic single-nucleotide variation in brain tissue of cases with schizophrenia
Q36362825	Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders
Q92915669	Assessment of the clinical utility of four NGS panels in myeloid malignancies. Suggestions for NGS panel choice or design
Q60305273	Association of Copy Number Variation at Intron 3 of With Navel Length in
Q36739874	Association of SNP Haplotypes of HKT Family Genes with Salt Tolerance in Indian Wild Rice Germplasm
Q36915060	Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Q35818746	Association of the Long Non-coding RNA Steroid Receptor RNA Activator (SRA) with TrxG and PRC2 Complexes
Q59348992	Atopic asthma after rhinovirus-induced wheezing is associated with DNA methylation change in the SMAD3 gene promoter
Q33733605	Atp8 is in the ground pattern of flatworm mitochondrial genomes
Q52320447	Atypical Tuberous Sclerosis Complex presenting as familial renal cell carcinoma with leiomyomatous stroma.
Q33640147	Automated multiplex genome-scale engineering in yeast
Q36291610	Autopolyploidy genome duplication preserves other ancient genome duplications in Atlantic salmon (Salmo salar)
Q48332656	Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation
Q37724131	A Frameshift Mutation in KIT is Associated with White Spotting in the Arabian Camel
Q89857184	A spontaneous complex structural variant in rcan-1 increases exploratory behavior and laboratory fitness of Caenorhabditis elegans
Q40043106	BA71ΔCD2: a New Recombinant Live Attenuated African Swine Fever Virus with Cross-Protective Capabilities.
Q37032991	BACH2 regulates CD8(+) T cell differentiation by controlling access of AP-1 factors to enhancers
Q38796886	BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing.
Q93160539	BAMscale: quantification of next-generation sequencing peaks and generation of scaled coverage tracks
Q31117800	BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment
Q30840115	BBCAnalyzer: a visual approach to facilitate variant calling
Q37622421	BCAS2 is involved in alternative mRNA splicing in spermatogonia and the transition to meiosis
Q90460722	BRAF Mutations and Dysregulation of the MAP Kinase Pathway Associated to Sinonasal Mucosal Melanomas
Q36175312	BRAF inhibitor vemurafenib improves the antitumor activity of adoptive cell immunotherapy
Q35140116	BRAF inhibitor-associated ERK activation drives development of chronic lymphocytic leukemia
Q98196799	BRAHMA-interacting proteins BRIP1 and BRIP2 are core subunits of Arabidopsis SWI/SNF complexes
Q36738744	BRCA somatic and germline mutation detection in paraffin embedded ovarian cancers by next-generation sequencing
Q97587324	BRCA1-associated structural variations are a consequence of polymerase theta-mediated end-joining
Q98471230	BRD4 prevents the accumulation of R-loops and protects against transcription-replication collision events and DNA damage
Q96136176	BRD4 promotes metastatic potential in oral squamous cell carcinoma through the epigenetic regulation of the MMP2 gene
Q97636085	BRD4 regulates key transcription factors that drive epithelial-mesenchymal transition in castration-resistant prostate cancer
Q57798553	BacCapSeq: a Platform for Diagnosis and Characterization of Bacterial Infections
Q38712033	Bach2 regulates AID-mediated immunoglobulin gene conversion and somatic hypermutation in DT40 B cells
Q90382862	Bacterial IAA-Delivery into Medicago Root Nodules Triggers a Balanced Stimulation of C and N Metabolism Leading to a Biomass Increase
Q36664581	Bacterial antisense RNAs are mainly the product of transcriptional noise
Q36486635	Bactobolin resistance is conferred by mutations in the L2 ribosomal protein.
Q28709644	BamView: visualizing and interpretation of next-generation sequencing read alignments
Q96303552	Basement membrane remodelling regulates mouse embryogenesis
Q52560201	Bcl11b is essential for licensing Th2 differentiation during helminth infection and allergic asthma.
Q64091463	Beta-catenin signaling regulates barrier-specific gene expression in circumventricular organ and ocular vasculatures
Q36269554	Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci.
Q60645374	Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia
Q42071978	BiQ Analyzer HiMod: an interactive software tool for high-throughput locus-specific analysis of 5-methylcytosine and its oxidized derivatives
Q42033622	Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration
Q92709292	Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia
Q41010751	Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases.
Q53499818	Biallelic mutations in NALCN: Expanding the genotypic and phenotypic spectra of IHPRF1.
Q64230617	Bidirectional Selection for Body Weight on Standing Genetic Variation in a Chicken Model
Q59352890	Bidirectional transfer of Anelloviridae lineages between graft and host during lung transplantation
Q91913311	Big Data to the Bench: Transcriptome Analysis for Undergraduates
Q35881016	BigQ: a NoSQL based framework to handle genomic variants in i2b2.
Q89089871	BioSankey: Visualization of Microbial Communities Over Time
Q39027949	Biogenesis and Transcriptional Regulation of Long Noncoding RNAs in the Human Immune System.
Q36374458	Bioinformatic Analysis for Profiling Drug-induced Chromatin Modification Landscapes in Mouse Brain Using ChlP-seq Data
Q31125559	Bioinformatic Analysis of ChIP-seq Data on the Repetitive Ribosomal RNA Gene
Q37834104	Bioinformatic analysis of bacteria and host cell dual RNA-sequencing experiments.
Q34295621	Bioinformatic approaches to augment study of epithelial-to-mesenchymal transition in lung cancer
Q39259719	Bioinformatics Analysis of Small RNA Transcriptomes: The Detailed Workflow
Q35016324	Bioinformatics approaches for viral metagenomics in plants using short RNAs: model case of study and application to a Cicer arietinum population
Q92882640	Bioinformatics of nanopore sequencing
Q34106505	Bioinformatics tools and databases for analysis of next-generation sequence data.
Q90975831	Biological plasticity rescues target activity in CRISPR knock outs
Q42710590	Biosynthesis of antinutritional alkaloids in solanaceous crops is mediated by clustered genes
Q58792941	Biotinylated amplicon sequencing: A method for preserving DNA samples of limited quantity
Q54224446	Birth, evolution, and transmission of satellite-free mammalian centromeric domains.
Q35148448	BisQC: an operational pipeline for multiplexed bisulfite sequencing
Q91280729	Bisulfite Sequence Analyses Using CyVerse Discovery Environment: From Mapping to DMRs
Q91907849	Bisulfite-free direct detection of 5-methylcytosine and 5-hydroxymethylcytosine at base resolution
Q37236777	BlackOPs: increasing confidence in variant detection through mappability filtering
Q62658161	Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis
Q64228378	Blimp1 Prevents Methylation of Foxp3 and Loss of Regulatory T Cell Identity at Sites of Inflammation
Q35847841	Blind study evaluation illustrates utility of the Ion PGM™ system for use in human identity DNA typing
Q92995104	Blocked O-GlcNAc cycling disrupts mouse hematopoeitic stem cell maintenance and early T cell development
Q52423023	Both CRISPR/Cas-based nucleases and nickases can be used efficiently for genome engineering in Arabidopsis thaliana.
Q38906935	Both maternally and paternally imprinted genes regulate seed development in rice
Q30416550	Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
Q58797665	Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity
Q36603763	Brevis plant1, a putative inositol polyphosphate 5-phosphatase, is required for internode elongation in maize
Q90290929	Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease
Q30653491	Browsing (Epi)genomes: a guide to data resources and epigenome browsers for stem cell researchers
Q35979104	Building a Robust Tumor Profiling Program: Synergy between Next-Generation Sequencing and Targeted Single-Gene Testing
Q36143915	Burkitt lymphoma beyond MYC translocation: N-MYC and DNA methyltransferases dysregulation
Q53126460	Bypassing Drug Resistance Mechanisms of Prostate Cancer with Small Molecules that Target Androgen Receptor-Chromatin Interactions.
Q41695687	C-State: an interactive web app for simultaneous multi-gene visualization and comparative epigenetic pattern search
Q40147015	C5orf42 is the major gene responsible for OFD syndrome type VI.
Q30989599	CADBURE: A generic tool to evaluate the performance of spliced aligners on RNA-Seq data
Q35892065	CANEapp: a user-friendly application for automated next generation transcriptomic data analysis
Q48957033	CAST-ChIP maps cell-type-specific chromatin states in the Drosophila central nervous system.
Q91823019	CBP Modulates Sensitivity to Dasatinib in Pre-BCR+ Acute Lymphoblastic Leukemia
Q41915296	CCT6A suppresses SMAD2 and promotes prometastatic TGF-β signaling
Q36097383	CD36 is involved in oleic acid detection by the murine olfactory system
Q89601652	CD8+ T Cells Require ITK-Mediated TCR Signaling for Migration to the Intestine
Q34449062	CDK7 inhibition suppresses super-enhancer-linked oncogenic transcription in MYCN-driven cancer.
Q47293995	CELSR2 is a candidate susceptibility gene in idiopathic scoliosis
Q35762931	CHARGE syndrome due to deletion of region upstream of CHD7 gene START codon
Q41510943	CHD1 regulates cell fate determination by activation of differentiation-induced genes
Q111442247	CMTR1 is recruited to transcription start sites and promotes ribosomal protein and histone gene expression in embryonic stem cells
Q94671631	CNN-Peaks: ChIP-Seq peak detection pipeline using convolutional neural networks that imitate human visual inspection
Q36909749	COHCAP: an integrative genomic pipeline for single-nucleotide resolution DNA methylation analysis
Q30753631	COV2HTML: a visualization and analysis tool of bacterial next generation sequencing (NGS) data for postgenomics life scientists
Q57232848	CPAP: Cancer Panel Analysis Pipeline
Q31003638	CRCDA--Comprehensive resources for cancer NGS data analysis
Q92822235	CRISPR Interference of a Clonally Variant GC-Rich Noncoding RNA Family Leads to General Repression of var Genes in Plasmodium falciparum
Q21133677	CRISPR-Cas systems in the cyanobacterium Synechocystis sp. PCC6803 exhibit distinct processing pathways involving at least two Cas6 and a Cmr2 protein
Q47144360	CRISPR-Cas9 mediated gene deletions in lager yeast Saccharomyces pastorianus
Q64065225	CRISPR/CAS9 targeted CAPTURE of mammalian genomic regions for characterization by NGS
Q33911270	CRISPR/Cas9 Genome Editing Reveals That the Intron Is Not Essential for var2csa Gene Activation or Silencing in Plasmodium falciparum
Q64388852	CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans
Q93180138	CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells
Q33826506	CRISPR/Cas9-mediated gene knockout screens and target identification via whole-genome sequencing uncover host genes required for picornavirus infection
Q92236967	CSA: a web service for the complete process of ChIP-Seq analysis
Q33732376	CTCF and cohesin regulate chromatin loop stability with distinct dynamics
Q36185754	CTCF-dependent co-localization of canonical Smad signaling factors at architectural protein binding sites in D. melanogaster
Q36595318	CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia
Q44765624	CWig: compressed representation of Wiggle/BedGraph format.
Q38740975	Cadherin-6 is a putative tumor suppressor and target of epigenetically dysregulated miR-429 in cholangiocarcinoma
Q41445381	Caenorhabditis elegans CES-1 Snail Represses pig-1 MELK Expression To Control Asymmetric Cell Division
Q92804633	Calling Star Alleles With Stargazer in 28 Pharmacogenes With Whole Genome Sequences
Q90623153	Can we use it? On the utility of de novo and reference-based assembly of Nanopore data for plant plastome sequencing
Q41138901	Cancer Driver Log (CanDL): Catalog of Potentially Actionable Cancer Mutations
Q37418530	Cancer exome analysis reveals a T-cell-dependent mechanism of cancer immunoediting
Q29615679	Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer
Q90907699	Cancer susceptibility gene mutations in type I and II endometrial cancer
Q40047777	Candidate gene molecular markers as tools for analyzing genetic susceptibility to Morbillivirus infection in stranded Cetaceans.
Q38978018	Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder
Q28818678	Candidate pathogenicity islands in the genome of 'Candidatus Rickettsiella isopodorum', an intracellular bacterium infecting terrestrial isopod crustaceans
Q35644929	Candidatus Frankia Datiscae Dg1, the Actinobacterial Microsymbiont of Datisca glomerata, Expresses the Canonical nod Genes nodABC in Symbiosis with Its Host Plant
Q33773663	Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2.
Q27318512	Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24
Q38390966	Capturing intra-tumor genetic heterogeneity by de novo mutation profiling of circulating cell-free tumor DNA: a proof-of-principle.
Q61031838	Capturing the Onset of PRC2-Mediated Repressive Domain Formation
Q50866622	Cardiac Fibroblast-Specific Activating Transcription Factor 3 Protects Against Heart Failure by Suppressing MAP2K3-p38 Signaling.
Q62782850	Cardiomyocytes have mosaic patterns of protein expression
Q37172278	Cardiovascular transcriptomics and epigenomics using next-generation sequencing: challenges, progress, and opportunities
Q34039369	Cas9 effector-mediated regulation of transcription and differentiation in human pluripotent stem cells
Q91622845	Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplications
Q64043732	Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice
Q49924865	Cas9-mediated excision of proximal DNaseI/H3K4me3 signatures confers robust silencing of microRNA and long non-coding RNA genes.
Q35904385	Cascade: an RNA-seq visualization tool for cancer genomics
Q39548128	Case report: on the use of the HID-Ion AmpliSeq™ Ancestry Panel in a real forensic case
Q33677756	Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
Q50207620	Catalytic-Independent Functions of PARP-1 Determine Sox2 Pioneer Activity at Intractable Genomic Loci.
Q38944374	Catch and Release: rare cell analysis from a functionalised medical wire
Q59132158	Causes and Consequences of a Variant Strain of With Reduced Competition
Q64884281	Cdk1 gates cell cycle-dependent tRNA synthesis by regulating RNA polymerase III activity.
Q97518482	Cell Type Impacts Accessibility of mRNA to Silencing by RNA Interference
Q37323160	Cell cycle progression in Caulobacter requires a nucleoid-associated protein with high AT sequence recognition
Q36341473	Cell type-specific genomics of Drosophila neurons
Q37596051	Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex.
Q49134689	Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition.
Q59329851	Cell-free DNA profiling of metastatic prostate cancer reveals microsatellite instability, structural rearrangements and clonal hematopoiesis
Q33915834	Cell-type specific differences in promoter activity of the ALS-linked C9orf72 mouse ortholog.
Q94070170	Cell-type-specific brain methylomes profiled via ultralow-input microfluidics
Q60921908	Cellular 5-hydroxylmethylcytosine content determines tumorigenic potential and prognosis of pancreatic ductal adenocarcinoma
Q90441070	Cellular reprogramming for successful CNS axon regeneration is driven by a temporally changing cast of transcription factors
Q91910470	Cellular response to moderate chromatin architectural defects promotes longevity
Q91641922	Cellular, transcriptomic and isoform heterogeneity of breast cancer cell line revealed by full-length single-cell RNA sequencing
Q49629799	Central role of the p53 pathway in the noncoding-RNA response to oxidative stress.
Q33663019	Cerebrospinal fluid-derived circulating tumour DNA better represents the genomic alterations of brain tumours than plasma.
Q90953584	Cervical cancer patients that respond to chemoradiation therapy display an intense tumor infiltrating immune profile before treatment
Q31130589	ChIA-PET2: a versatile and flexible pipeline for ChIA-PET data analysis
Q92893031	ChIP and Chips: Introducing the WormPharm for correlative studies employing pharmacology and genome-wide analyses in C. elegans
Q58563673	ChIP-Atlas: a data-mining suite powered by full integration of public ChIP-seq data
Q51354115	ChIP-seq Analysis of Condensin Complex in Cultured Mammalian Cells.
Q31132639	ChIP-seq Data Processing for PcG Proteins and Associated Histone Modifications.
Q33830443	ChIP-seq analysis of genomic binding regions of five major transcription factors highlights a central role for ZIC2 in the mouse epiblast stem cell gene regulatory network.
Q51418192	ChIP-seq and ChIP-exo profiling of Pol II, H2A.Z, and H3K4me3 in human K562 cells.
Q38851252	ChIP-seq in studying epigenetic mechanisms of disease and promoting precision medicine: progresses and future directions
Q64067224	ChIPulate: A comprehensive ChIP-seq simulation pipeline
Q92260714	Challenges in funding and developing genomic software: roots and remedies
Q89884662	Challenges in identifying large germline structural variants for clinical use by long read sequencing
Q51418858	Changes at the nuclear lamina alter binding of pioneer factor Foxa2 in aged liver.
Q93073871	Changes in chromatin accessibility ensure robust cell cycle exit in terminally differentiated cells
Q34605887	Changes in nucleosome occupancy associated with metabolic alterations in aged mammalian liver
Q36055559	Characterisation of CDKL5 Transcript Isoforms in Human and Mouse
Q93061294	Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs
Q34472208	Characteristics of de novo structural changes in the human genome
Q92491555	Characteristics of induced mutations in offspring derived from irradiated mouse spermatogonia and mature oocytes
Q40865336	Characterization and comparative analysis of a simian foamy virus complete genome isolated from Brazilian capuchin monkeys
Q57462250	Characterization of Alternative Splicing Events in HPV-Negative Head and Neck Squamous Cell Carcinoma Identifies an Oncogenic DOCK5 Variant
Q37122501	Characterization of Clostridium difficile Spores Lacking Either SpoVAC or Dipicolinic Acid Synthetase.
Q58786657	Characterization of Factors Affecting the Detection Limit of EGFR p.T790M in Circulating Tumor DNA
Q41920916	Characterization of Three New Insect-Specific Flaviviruses: Their Relationship to the Mosquito-Borne Flavivirus Pathogens
Q21131890	Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing
Q39747574	Characterization of a New Pink-Fruited Tomato Mutant Results in the Identification of a Null Allele of the SlMYB12 Transcription Factor.
Q91899658	Characterization of a Novel Conjugative Plasmid in Edwardsiella piscicida Strain MS-18-199
Q35861569	Characterization of an APC Promoter 1B deletion in a Patient Diagnosed with Familial Adenomatous Polyposis via Whole Genome Shotgun Sequencing
Q42334823	Characterization of an androgen-responsive, ornithine decarboxylase-related protein in mouse kidney.
Q24633977	Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing
Q36809494	Characterization of eukaryotic DNA N(6)-methyladenine by a highly sensitive restriction enzyme-assisted sequencing
Q40765189	Characterization of functionally active gene fusions in human papillomavirus related oropharyngeal squamous cell carcinoma
Q33691435	Characterization of genetic aberrations in a single case of metastatic thymic adenocarcinoma
Q91526219	Characterization of genetic subclonal evolution in pancreatic cancer mouse models
Q91143231	Characterization of human telomerase reverse transcriptase promoter methylation and transcription factor binding in differentiated thyroid cancer cell lines
Q92831842	Characterization of intellectual disability and autism comorbidity through gene panel sequencing
Q91855473	Characterization of novel genetic alterations in salivary gland secretory carcinoma
Q55044852	Characterization of phenotypic variation and genome aberrations observed among Phytophthora ramorum isolates from diverse hosts.
Q35679188	Characterization of pseudorabies virus transcriptome by Illumina sequencing
Q41873815	Characterization of the genomic architecture and mutational spectrum of a small cell prostate carcinoma
Q33579776	Characterization of the genomic features and expressed fusion genes in micropapillary carcinomas of the breast
Q54769753	Characterization of translocations in mesenchymal hamartoma and undifferentiated embryonal sarcoma of the liver.
Q40041460	Characterization of vB_SauM-fRuSau02, a Twort-Like Bacteriophage Isolated from a Therapeutic Phage Cocktail
Q49830216	Characterization of viral RNA splicing using whole-transcriptome datasets from host species.
Q62648595	Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis
Q30423222	Characterizing complex structural variation in germline and somatic genomes
Q96817033	Chd4 choreographs self-antigen expression for central immune tolerance
Q90254830	Chemically defined and growth-factor-free culture system for the expansion and derivation of human pluripotent stem cells
Q55301513	Chikungunya virus evolution following a large 3'UTR deletion results in host-specific molecular changes in protein-coding regions.
Q22122062	Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite
Q47991934	Chimeric NUP98-NSD1 transcripts from the cryptic t(5;11)(q35.2;p15.4) in adult de novo acute myeloid leukemia.
Q36313731	Chironomus riparius (Diptera) genome sequencing reveals the impact of minisatellite transposable elements on population divergence.
Q35710313	Chlamydia trachomatis In Vivo to In Vitro Transition Reveals Mechanisms of Phase Variation and Down-Regulation of Virulence Factors
Q40607219	Chlamydomonas Genome Resource for Laboratory Strains Reveals a Mosaic of Sequence Variation, Identifies True Strain Histories, and Enables Strain-Specific Studies.
Q37612740	Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts
Q90628419	Chromatin Remodeling and Immediate Early Gene Activation by SLFN11 in Response to Replication Stress
Q89972715	Chromatin accessibility and histone acetylation in the regulation of competence in early development
Q58541925	Chromatin accessibility dynamics across development and ageing
Q91891585	Chromatin architecture reorganization in murine somatic cell nuclear transfer embryos
Q60919328	Chromatin changes in Anopheles gambiae induced by Plasmodium falciparum infection
Q57046190	Chromatin conformation and transcriptional activity are permissive regulators of DNA replication initiation in Drosophila
Q38380810	Chromatin immunoprecipitation from fixed clinical tissues reveals tumor-specific enhancer profiles
Q92475989	Chromatin interactome mapping at 139 independent breast cancer risk signals
Q35589997	Chromatin mediation of a transcriptional memory effect in yeast
Q34056411	Chromatin profiling reveals regulatory network shifts and a protective role for hepatocyte nuclear factor 4α during colitis.
Q47256163	Chromatin state changes during neural development revealed by in vivo cell-type specific profiling
Q46060358	Chromatin states define tumour-specific T cell dysfunction and reprogramming.
Q113240289	Chromatin structure can introduce systematic biases in genome-wide analyses of Plasmodium falciparum
Q61811556	Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes
Q51416607	Chromium disrupts chromatin organization and CTCF access to its cognate sites in promoters of differentially expressed genes.
Q36574545	Chromoanasynthetic Genomic Rearrangement Identified in a N-Ethyl-N-Nitrosourea (ENU) Mutagenesis Screen in Caenorhabditis elegans
Q37181911	Chromosomal landscape of UV damage formation and repair at single-nucleotide resolution
Q39034749	Chromosome fragility and the abnormal replication of the FMR1 locus in fragile X syndrome
Q91782818	Chromosome-Level Alpaca Reference Genome VicPac3.1 Improves Genomic Insight Into the Biology of New World Camelids
Q37420357	Chromosome-wide profiling of X-chromosome inactivation and epigenetic states in fetal brain and placenta of the opossum, Monodelphis domestica
Q47758630	Cic Loss Promotes Gliomagenesis via Aberrant Neural Stem Cell Proliferation and Differentiation.
Q46268195	CircView: a visualization and exploration tool for circular RNAs.
Q34318374	Circular RNAs are abundant, conserved, and associated with ALU repeats
Q37661448	Circulating tumor cells capture disease evolution in advanced prostate cancer.
Q88595919	Cisplatin-DNA adduct repair of transcribed genes is controlled by two circadian programs in mouse tissues
Q93270744	Cistrome Data Browser: expanded datasets and new tools for gene regulatory analysis
Q44240808	Clarifying sub-genomic positions of QTLs for flowering habit and fruit quality in U.S. strawberry (Fragaria×ananassa) breeding populations using pedigree-based QTL analysis
Q21183997	Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors
Q91930500	Classroom as Genome: Using the Tools of Genomics and Bioinformatics to Illuminate Classroom Observation Data
Q60907416	Claudin-3-deficient C57BL/6J mice display intact brain barriers
Q48143317	Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR-CCNB3 gene fusion
Q48270517	Click chemistry enables preclinical evaluation of targeted epigenetic therapies.
Q92965867	Clinical and molecular characterization of patients with acute myeloid leukemia and sole trisomies of chromosomes 4, 8, 11, 13 or 21
Q30489035	Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis.
Q35900361	Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms
Q37599237	Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Q92129104	Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Q98564426	Clinical implications of prospective genomic profiling of metastatic breast cancer patients
Q91659636	Clinical mutational profiling and categorization of BRAF mutations in melanomas using next generation sequencing
Q92712432	Clinical relevance of somatic mutations in main driver genes detected in gastric cancer patients by next-generation DNA sequencing
Q89120437	Clinical response of the novel activating ALK-I1171T mutation in neuroblastoma to the ALK inhibitor ceritinib
Q89518987	Clinical significance of TP53, BIRC3, ATM and MAPK-ERK genes in chronic lymphocytic leukaemia: data from the randomised UK LRF CLL4 trial
Q61808912	Clinical significance of the mutational landscape and fragmentation of circulating tumor DNA in renal cell carcinoma
Q48348934	Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors.
Q33787472	Clinical utility of whole-exome sequencing in rare diseases: Galactosialidosis
Q92638496	Clinical, histopathological and genetic characterisation of oculoskeletal dysplasia in the Northern Inuit Dog
Q52611832	Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing.
Q41233667	Clinically significant sub-clonality for common drivers can be detected in 26% of KRAS/EGFR mutated lung adenocarcinomas.
Q90480973	Clinicopathological characteristics and genetic analysis of pulmonary carcinoid tumors: A single-center retrospective cohort study and literature review
Q57073246	Clinker: visualizing fusion genes detected in RNA-seq data
Q64067290	Clipped histone H3 is integrated into nucleosomes of DNA replication genes in the human malaria parasite
Q89967098	Clonal Hematopoiesis From Next Generation Sequencing of Plasma From a Patient With Lung Adenocarcinoma: A Case Report
Q36925503	Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition
Q89776891	Clonal evolution underlying leukemia progression and Richter transformation in patients with ibrutinib-relapsed CLL
Q46192438	Clonal hematopoiesis in patients with dyskeratosis congenita
Q96348568	Clonal hematopoiesis is associated with adverse outcomes in multiple myeloma patients undergoing transplant
Q37173548	Clonal neoantigens elicit T cell immunoreactivity and sensitivity to immune checkpoint blockade
Q36176934	Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.
Q91854850	Co-incidence of RCC-susceptibility polymorphisms with HIF cis-acting sequences supports a pathway tuning model of cancer
Q47133201	Co-regulation of transcription by BRG1 and BRM, two mutually exclusive SWI/SNF ATPase subunits
Q92371782	CoCo: RNA-seq read assignment correction for nested genes and multimapped reads
Q91651372	Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging
Q36031029	Codon Usage Influences the Local Rate of Translation Elongation to Regulate Co-translational Protein Folding
Q96641068	Cohesin promotes stochastic domain intermingling to ensure proper regulation of boundary-proximal genes
Q38485000	Collaborative regulation of development but independent control of metabolism by two epidermis-specific transcription factors in Caenorhabditis elegans
Q30768176	Collection, integration and analysis of cancer genomic profiles: from data to insight
Q64929020	Combination of flow cytometry and functional imaging for monitoring of residual disease in myeloma.
Q83224291	Combinatorial chromatin dynamics foster accurate cardiopharyngeal fate choices
Q42365553	Combinatorial control of gene expression in Aspergillus niger grown on sugar beet pectin
Q42500574	Combinatorial epigenetic regulation of non-coding RNAs has profound effects on oncogenic pathways in breast cancer subtypes
Q88923140	Combinatorial knockout of RARα, RARβ, and RARγ completely abrogates transcriptional responses to retinoic acid in murine embryonic stem cells
Q34582354	Combined ChIP-Seq and transcriptome analysis identifies AP-1/JunD as a primary regulator of oxidative stress and IL-1β synthesis in macrophages
Q51419168	Combined cistrome and transcriptome analysis of SKI in AML cells identifies SKI as a co-repressor for RUNX1.
Q35120513	Combined melanocytic and sweat gland neoplasm: cell subsets harbor an identical HRAS mutation in phacomatosis pigmentokeratotica
Q48153693	Combined tumor genomic profiling and exome sequencing in a breast cancer family implicates ATM in tumorigenesis: A proof of principle study
Q58599357	Combining STING-based neoantigen-targeted vaccine with checkpoint modulators enhances antitumor immunity in murine pancreatic cancer
Q90170691	Combining short and long read sequencing to characterize antimicrobial resistance genes on plasmids applied to an unauthorized genetically modified Bacillus
Q36867676	Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection
Q37241472	Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits
Q55380392	Common and divergent features of galactose-1-phosphate and fructose-1-phosphate toxicity in yeast.
Q53636047	Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis.
Q37236012	Common fusion transcripts identified in colorectal cancer cell lines by high-throughput RNA sequencing
Q97538221	Comparable cancer-relevant mutation profiles in synchronous ductal carcinoma in situ and invasive breast cancer
Q90646235	Comparative Analysis of Gammaherpesvirus Circular RNA Repertoires: Conserved and Unique Viral Circular RNAs
Q49895243	Comparative Analysis of Immune Cells Reveals a Conserved Regulatory Lexicon.
Q28550169	Comparative Life Cycle Transcriptomics Revises Leishmania mexicana Genome Annotation and Links a Chromosome Duplication with Parasitism of Vertebrates
Q58586609	Comparative Study on Alternative Splicing in Human Fungal Pathogens Suggests Its Involvement During Host Invasion
Q90071056	Comparative Transcriptome Analysis Reveals Different Host Cell Responses to Acute and Persistent Foot-and-Mouth Disease Virus Infection
Q36034801	Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Q38838300	Comparative analysis of de novo assemblers for variation discovery in personal genomes
Q34942970	Comparative analysis of non-coding RNAs in the antibiotic-producing Streptomyces bacteria
Q47152822	Comparative analysis of primary versus relapse/refractory DLBCL identifies shifts in mutation spectrum
Q34693423	Comparative analysis of the peanut witches'-broom phytoplasma genome reveals horizontal transfer of potential mobile units and effectors.
Q92539957	Comparative analysis on the expression of L1 loci using various RNA-Seq preparations
Q39038992	Comparative and retrospective molecular analysis of Parapoxvirus (PPV) isolates
Q90303408	Comparative genome analysis of Aspergillus flavus clinically isolated in Japan
Q35746800	Comparative genome analysis of Mycoplasma pneumoniae
Q42220191	Comparative genome analysis of Pseudomonas knackmussii B13, the first bacterium known to degrade chloroaromatic compounds
Q34550033	Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium.
Q89661724	Comparative genome characterization of the periodontal pathogen Tannerella forsythia
Q64243951	Comparative genomic analysis of eight novel haloalkaliphilic bacteriophages from Lake Elmenteita, Kenya
Q37317214	Comparative genomic analysis of primary tumors and metastases in breast cancer.
Q28651134	Comparative genomics reveals molecular features unique to the songbird lineage
Q33872148	Comparative genomics shows that viral integrations are abundant and express piRNAs in the arboviral vectors Aedes aegypti and Aedes albopictus
Q36268076	Comparative oncogenomics implicates the neurofibromin 1 gene (NF1) as a breast cancer driver.
Q44079870	Comparative phenotypic analysis and genome sequence of Clostridium beijerinckii SA-1, an offspring of NCIMB 8052.
Q60924390	Comparative study for haplotype block partitioning methods - Evidence from chromosome 6 of the North American Rheumatoid Arthritis Consortium (NARAC) dataset
Q61445820	Comparative transcriptomic analysis unveils interactions between the regulatory CarS protein and light response in Fusarium
Q33868427	Comparative transcriptomics uncovers alternative splicing and molecular marker development in radish (Raphanus sativus L.).
Q90100003	Comparison and Characterization of Mutations Induced by Gamma-Ray and Carbon-Ion Irradiation in Rice (Oryza sativa L.) Using Whole-Genome Resequencing
Q38845359	Comparison of Ion Personal Genome Machine Platforms for the Detection of Variants in BRCA1 and BRCA2.
Q38827665	Comparison of Spinach Sex Chromosomes with Sugar Beet Autosomes Reveals Extensive Synteny and Low Recombination at the Male-Determining Locus.
Q34786626	Comparison of custom capture for targeted next-generation DNA sequencing
Q39157730	Comparison of exome-based HLA class I genotyping tools: identification of platform-specific genotyping errors
Q37145149	Comparison of metabolic capacities and inference of gene content evolution in mosquito-associated Spiroplasma diminutum and S. taiwanense
Q92777623	Comparison of multiple algorithms to reliably detect structural variants in pears
Q34034198	Comparison of solution-based exome capture methods for next generation sequencing
Q39476678	Comparison of targeted next-generation sequencing (NGS) and real-time PCR in the detection of EGFR, KRAS, and BRAF mutations on formalin-fixed, paraffin-embedded tumor material of non-small cell lung carcinoma-superiority of NGS.
Q30976546	Comparison of the Equine Reference Sequence with Its Sanger Source Data and New Illumina Reads
Q57301223	Comparison of the Genetic Alterations between Primary Colorectal Cancers and Their Corresponding Patient-Derived Xenograft Tissues
Q38831184	Comparison of the Life Cycles of Genetically Distant Species C and Species D Human Adenoviruses Ad6 and Ad26 in Human Cells
Q88869223	Competence inhibition by the XrpA peptide encoded within the comX gene of Streptococcus mutans
Q35301426	Competition between ADAR and RNAi pathways for an extensive class of RNA targets
Q34460404	Complete Genome Sequence of "Candidatus Sulcia muelleri" ML, an Obligate Nutritional Symbiont of Maize Leafhopper (Dalbulus maidis).
Q55025371	Complete Genome Sequence of Agrobacterium tumefaciens 1D1609.
Q35687205	Complete Genome Sequence of Agrobacterium tumefaciens Ach5.
Q64089603	Complete Genome Sequence of Spiroplasma alleghenense PLHS-1 (ATCC 51752), a Bacterium Isolated from Scorpion Fly ()
Q37458420	Complete Genome Sequence of Spiroplasma apis B31T (ATCC 33834), a Bacterium Associated with May Disease of Honeybees (Apis mellifera).
Q36193095	Complete Genome Sequence of Spiroplasma cantharicola CC-1T (DSM 21588), a Bacterium Isolated from Soldier Beetle (Cantharis carolinus).
Q41117690	Complete Genome Sequence of Spiroplasma corruscae EC-1T (DSM 19793), a Bacterium Isolated from a Lampyrid Beetle (Ellychnia corrusca).
Q54995669	Complete Genome Sequence of Spiroplasma floricola 23-6T (ATCC 29989), a Bacterium Isolated from a Tulip Tree (Liriodendron tulipifera L.).
Q37355417	Complete Genome Sequence of Spiroplasma helicoides TABS-2T (DSM 22551), a Bacterium Isolated from a Horsefly (Tabanus abactor).
Q36113912	Complete Genome Sequence of Spiroplasma litorale TN-1T (DSM 21781), a Bacterium Isolated from a Green-Eyed Horsefly (Tabanus nigrovittatus).
Q55101257	Complete Genome Sequence of Spiroplasma monobiae MQ-1T (ATCC 33825), a Bacterium Isolated from the Vespid Wasp (Monobia quadridens).
Q37695482	Complete Genome Sequence of Spiroplasma sp. NBRC 100390.
Q37599705	Complete Genome Sequence of Spiroplasma sp. TU-14.
Q37277671	Complete Genome Sequence of Spiroplasma turonicum Tab4cT, a Bacterium Isolated from Horse Flies (Haematopota sp.).
Q41153439	Complete Genome Sequence of Tomato Mosaic Virus Isolated from Jasmine in the United States
Q34283834	Complete Genome Sequence of Vibrio vulnificus 93U204, a Bacterium Isolated from Diseased Tilapia in Taiwan
Q92526166	Complete Genome Sequences for Two Talaromyces marneffei Clinical Isolates from Northern and Southern Vietnam
Q91592788	Complete Genome Sequences of 10 Xanthomonas oryzae pv. oryzae Bacteriophages
Q64060341	Complete Genome Sequences of Four Serotypes of Dengue Virus Prototype Continuously Maintained in the Laboratory
Q49480890	Complete Genome Sequences of Four Toxigenic Clostridium difficile Clinical Isolates from Patients of the Lower Hudson Valley, New York, USA.
Q34497206	Complete Mitochondrial Genomes of New Zealand's First Dogs
Q36162588	Complete Sequence and Analysis of Coconut Palm (Cocos nucifera) Mitochondrial Genome
Q64110838	Complete assembly of the Leishmania donovani (HU3 strain) genome and transcriptome annotation
Q34514653	Complete chloroplast genome sequence of Omani lime (Citrus aurantiifolia) and comparative analysis within the rosids
Q36406391	Complete chloroplast genome sequence of common bermudagrass (Cynodon dactylon (L.) Pers.) and comparative analysis within the family Poaceae
Q40136889	Complete genome sequence of Ostreid herpesvirus type 1 µVar isolated during mortality events in the Pacific oyster Crassostrea gigas in France and Ireland
Q42150871	Complete genome sequence of a tomato mottle mosaic virus isolate from the United States
Q45733856	Complete genome sequence of the mitochondrial DNA of the river lamprey, Lethenteron japonicum.
Q43603525	Complete genome sequence of the mitochondrial DNA of the sparkling enope squid, Watasenia scintillans.
Q36974654	Complete genomes of two dipteran-associated spiroplasmas provided insights into the origin, dynamics, and impacts of viral invasion in spiroplasma
Q51042797	Complete genomic landscape of a recurring sporadic parathyroid carcinoma.
Q36851425	Complete hematologic response of early T-cell progenitor acute lymphoblastic leukemia to the γ-secretase inhibitor BMS-906024: genetic and epigenetic findings in an outlier case
Q34701758	Complete plastid genome sequence of the basal asterid Ardisia polysticta Miq. and comparative analyses of asterid plastid genomes
Q37430071	Complex tissue-specific patterns and distribution of multiple RAGE splice variants in different mammals
Q50955653	Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome.
Q33399905	Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
Q94525825	Comprehensive Analysis of CDC27 Related to Peritoneal Metastasis by Whole Exome Sequencing in Gastric Cancer
Q35839601	Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
Q61053903	Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
Q35966298	Comprehensive Definition of the SigH Regulon of Mycobacterium tuberculosis Reveals Transcriptional Control of Diverse Stress Responses
Q93047934	Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort
Q41613769	Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency.
Q36563549	Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes
Q35075158	Comprehensive analysis of transcriptome variation uncovers known and novel driver events in T-cell acute lymphoblastic leukemia
Q92683025	Comprehensive annotations of human herpesvirus 6A and 6B genomes reveal novel and conserved genomic features
Q38930324	Comprehensive characterization of genes associated with the TP53 signal transduction pathway in various tumors
Q36111215	Comprehensive comparison of molecular portraits between cell lines and tumors in breast cancer
Q38973884	Comprehensive evaluation of de novo transcriptome assembly programs and their effects on differential gene expression analysis
Q49199812	Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.
Q92262647	Comprehensive genomic profiling of high-grade serous ovarian carcinoma from Chinese patients identifies co-occurring mutations in the Ras/Raf pathway with TP53
Q94554231	Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors
Q34262286	Comprehensive high-throughput RNA sequencing analysis reveals contamination of multiple nasopharyngeal carcinoma cell lines with HeLa cell genomes
Q37193365	Comprehensive mutation profiling by next-generation sequencing of effusion fluids from patients with high-grade serous ovarian carcinoma
Q42367352	Comprehensive screening of target molecules by next-generation sequencing in patients with malignant solid tumors: guiding entry into phase I clinical trials
Q64234563	Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements
Q30698740	Compression of structured high-throughput sequencing data
Q34491794	Compromised RNA polymerase III complex assembly leads to local alterations of intergenic RNA polymerase II transcription in Saccharomyces cerevisiae
Q28686251	Computational analysis of bacterial RNA-Seq data
Q38335021	Computational and analytical challenges in single-cell transcriptomics
Q38367824	Computational methodology for ChIP-seq analysis
Q36976457	Concentrating pre-mRNA processing factors in the histone locus body facilitates efficient histone mRNA biogenesis.
Q92334597	Concomitant and noncanonical JAK2 and MPL mutations in JAK2V617F- and MPLW515 L-positive myelofibrosis
Q55115047	Concurrent Host-Pathogen Transcriptional Responses in a Clostridium perfringens Murine Myonecrosis Infection.
Q40997916	Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome
Q35916990	Condensin targets and reduces unwound DNA structures associated with transcription in mitotic chromosome condensation
Q90628480	Conditional Single Vector CRISPR/SaCas9 Viruses for Efficient Mutagenesis in the Adult Mouse Nervous System
Q53915700	Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion.
Q34476085	Congenital cataracts: de novo gene conversion event in CRYBB2.
Q37725864	Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis
Q93183187	Conidial Morphogenesis and Septin-Mediated Plant Infection Require Smo1, a Ras GTPase-Activating Protein in Magnaporthe oryzae
Q34310269	Consensus rules in variant detection from next-generation sequencing data
Q89393079	Conservation of mRNA quality control factor Ski7 and its diversification through changes in alternative splicing and gene duplication
Q38429205	Conserved Transcription Factors Steer Growth-Related Genomic Programs in Daphnia
Q38935229	Conserved effect of aging on DNA methylation and association with EZH2 polycomb protein in mice and humans
Q45036014	Conserved regulation of hoxc11 by pitx1 in Anolis lizards
Q47659265	Considerations on Experimental Design and Data Analysis of Chromatin Immunoprecipitation Experiments
Q93163087	Consistent RNA sequencing contamination in GTEx and other data sets
Q35460011	Construction of a mariner-based transposon vector for use in insertion sequence mutagenesis in selected members of the Rhizobiaceae
Q48204405	Construction of full-length Japanese reference panel of class I HLA genes with single-molecule, real-time sequencing.
Q92610027	Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex
Q44877047	Contemporary evolution of a Lepidopteran species, Heliothis virescens, in response to modern agricultural practices
Q38810340	Context-Specific Effects of TGF-β/SMAD3 in Cancer Are Modulated by the Epigenome.
Q21266675	ContigScape: a Cytoscape plugin facilitating microbial genome gap closing
Q91780889	Continuous and Discrete Neuron Types of the Adult Murine Striatum
Q91723135	Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing
Q28242188	Contribution of RIT1 mutations to the pathogenesis of Noonan syndrome: four new cases and further evidence of heterogeneity
Q37502181	Contribution of natural antisense transcription to an endogenous siRNA signature in human cells.
Q90724417	Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration
Q33363945	Control of Oriented Tissue Growth through Repression of Organ Boundary Genes Promotes Stem Morphogenesis
Q58741724	Control of directionality of chromatin folding for the inter- and intra-domain contacts at the Tfap2c-Bmp7 locus
Q92784867	Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation
Q47448307	Control of nerve cord formation by Engrailed and Gooseberry-Neuro: A multi-step, coordinated process.
Q46623774	Control of plant cell fate transitions by transcriptional and hormonal signals.
Q94530153	Controlling gene activation by enhancers through a drug-inducible topological insulator
Q49340216	Conventional and pioneer modes of glucocorticoid receptor interaction with enhancer chromatin in vivo.
Q92751151	Convergent genetic aberrations in murine and human T lineage acute lymphoblastic leukemias
Q46475999	Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals
Q41691913	Cooperative interactions enable singular olfactory receptor expression in mouse olfactory neurons
Q60914617	Cooperative predation in the social amoebae Dictyostelium discoideum
Q42124699	Coordinate Regulation of Antimycin and Candicidin Biosynthesis
Q41861562	Coordinate redeployment of PRC1 proteins suppresses tumor formation during Drosophila development
Q90442116	Coordinated alterations in RNA splicing and epigenetic regulation drive leukaemogenesis
Q92203631	Coordinated transcriptional regulation by thyroid hormone and glucocorticoid interaction in adult mouse hippocampus-derived neuronal cells
Q58113988	Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic Patients
Q58703328	Copy number variation is associated with gene expression change in archaea
Q54936179	Core non-coding RNAs of Piscirickettsia salmonis.
Q37732569	Coregulation of genetic programs by the transcription factors NFIB and STAT5.
Q36131210	Correction of Down syndrome and Edwards syndrome aneuploidies in human cell cultures
Q45370513	Correction of a pathogenic gene mutation in human embryos
Q39227619	Correlation of B7-H3 with androgen receptor, immune pathways and poor outcome in prostate cancer: an expression-based analysis
Q64097680	Corrupted coordination of epigenetic modifications leads to diverging chromatin states and transcriptional heterogeneity in CLL
Q47270556	Coupling of microRNA-directed phased small interfering RNA generation from long noncoding genes with alternative splicing and alternative polyadenylation in small RNA-mediated gene silencing.
Q30676015	Coval: improving alignment quality and variant calling accuracy for next-generation sequencing data.
Q38615870	Crambled: A Shiny application to enable intuitive resolution of conflicting cellularity estimates
Q92129130	Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis
Q57040708	Cross-resistance is modular in bacteria-phage interactions
Q97587326	Cross-species oncogenic signatures of breast cancer in canine mammary tumors
Q92086343	Crosstalk between chromatin structure, cohesin activity and transcription
Q46268357	Cultivation of Peptidiphaga gingivicola from subgingival plaque: The first representative of a novel genus of Actinomycetaceae
Q37037117	Cutaneous squamous and neuroendocrine carcinoma: genetically and immunohistochemically different from Merkel cell carcinoma
Q64232923	Cyclical adaptation of measles virus quasispecies to epithelial and lymphocytic cells: To V, or not to V
Q59790638	Cyclin A2/E1 activation defines a hepatocellular carcinoma subclass with a rearrangement signature of replication stress
Q99243096	Cytogenetically visible inversions are formed by multiple molecular mechanisms
Q38895948	Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis
Q33607399	DDK Promotes Tumor Chemoresistance and Survival via Multiple Pathways.
Q46261088	DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes.
Q47141399	DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition
Q30410672	DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma
Q47397800	DISARM is a widespread bacterial defence system with broad anti-phage activities.
Q39858965	DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System
Q64388374	DNA Ligase 1 is an essential mediator of sister chromatid telomere fusions in G2 cell cycle phase
Q57030104	DNA damage sensitivity of SWI/SNF-deficient cells depends on TFIIH subunit p62/GTF2H1
Q33685402	DNA methylation and Transcriptome Changes Associated with Cisplatin Resistance in Ovarian Cancer
Q47113975	DNA methylation in silkworm genome may provide insights into epigenetic regulation of response to Bombyx mori cypovirus infection
Q57474637	DNA methylation patterns in peripheral blood mononuclear cells from Holstein cattle with variable milk yield
Q31133498	DNA methylation profiling of the fibrinogen gene landscape in human cells and during mouse and zebrafish development
Q64071456	DNA methylation repels targeting of Arabidopsis REF6
Q64064309	DNA methylome of human neonatal umbilical cord: Enrichment of differentially methylated regions compared to umbilical cord blood DNA at transcription factor genes involved in body patterning and effects of maternal folate deficiency or children's sex
Q46242671	DNA mismatch repair preferentially protects genes from mutation
Q37125781	DNA repair genes are selectively mutated in diffuse large B cell lymphomas
Q39030647	DNA sequence properties that predict susceptibility to epiallelic switching.
Q47903841	DNA sequencing at 40: past, present and future
Q38388740	DNAseq Workflow in a Diagnostic Context and an Example of a User Friendly Implementation
Q65000831	DNase-seq to Study Chromatin Accessibility in Early Xenopus tropicalis Embryos.
Q37179299	DOT1L-mediated H3K79me2 modification critically regulates gene expression during cardiomyocyte differentiation
Q35053069	DUX4 binding to retroelements creates promoters that are active in FSHD muscle and testis
Q35190362	DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy
Q36300839	DUX4-induced dsRNA and MYC mRNA stabilization activate apoptotic pathways in human cell models of facioscapulohumeral dystrophy
Q28115665	DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects
Q38425165	Dalliance: interactive genome viewing on the web.
Q38996216	Dataset for distribution of SIDER2 elements in the Leishmania major genome and transcriptome.
Q35998049	De Novo Centromere Formation and Centromeric Sequence Expansion in Wheat and its Wide Hybrids
Q89462013	De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus
Q28297699	De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy
Q38474294	De novo characterisation of the greenlip abalone transcriptome (Haliotis laevigata) with a focus on the heat shock protein 70 (HSP70) family.
Q61780809	De novo clustering of long reads by gene from transcriptomics data
Q24627067	De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
Q37693369	De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability
Q91814933	De novo mutation rate estimation in wolves of known pedigree
Q21144861	De novo mutations in moderate or severe intellectual disability
Q28260677	De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome
Q34508599	De novo reconstruction of the Toxoplasma gondii transcriptome improves on the current genome annotation and reveals alternatively spliced transcripts and putative long non-coding RNAs
Q28715973	De novo sequence assembly and characterisation of a partial transcriptome for an evolutionarily distinct reptile, the tuatara (Sphenodon punctatus)
Q41821972	De novo sequencing, assembly and analysis of the genome of the laboratory strain Saccharomyces cerevisiae CEN.PK113-7D, a model for modern industrial biotechnology
Q29615950	De novo transcript sequence reconstruction from RNA-seq using the Trinity platform for reference generation and analysis
Q91497049	De novo variation in bipolar disorder
Q34217540	De-novo assembly and analysis of the heterozygous triploid genome of the wine spoilage yeast Dekkera bruxellensis AWRI1499.
Q58617533	Deciphering highly similar multigene family transcripts from Iso-Seq data with IsoCon
Q91143059	Deciphering the genomic, epigenomic, and transcriptomic landscapes of pre-invasive lung cancer lesions
Q41159611	Deciphering the metabolic response of Mycobacterium tuberculosis to nitrogen stress
Q35970681	Deciphering the plant splicing code: experimental and computational approaches for predicting alternative splicing and splicing regulatory elements
Q41612823	Decitabine-Vorinostat combination treatment in acute myeloid leukemia activates pathways with potential for novel triple therapy
Q101569793	Decoding myofibroblast origins in human kidney fibrosis
Q37629378	Deep Assessment of Genomic Diversity in Cassava for Herbicide Tolerance and Starch Biosynthesis.
Q36117450	Deep Sequencing Analysis of Nucleolar Small RNAs: Bioinformatics
Q37142077	Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation and homozygous truncating mutations
Q54453253	Deep proteome profiling of Trichoplax adhaerens reveals remarkable features at the origin of metazoan multicellularity.
Q38759537	Deep sequencing and high-throughput analysis of PIWI-associated small RNAs.
Q34974058	Deep sequencing identifies genetic heterogeneity and recurrent convergent evolution in chronic lymphocytic leukemia
Q92887487	Deep sequencing of a recurrent oligodendroglioma and the derived xenografts reveals new insights into the evolution of human oligodendroglioma and candidate driver genes
Q33892571	Deep sequencing of organ- and stage-specific microRNAs in the evolutionarily basal insect Blattella germanica (L.) (Dictyoptera, Blattellidae).
Q34311583	Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.
Q41141837	Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease
Q36576392	Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis
Q91924566	DeepSV: accurate calling of genomic deletions from high-throughput sequencing data using deep convolutional neural network
Q43045026	Defect in the formation of 70S ribosomes caused by lack of ribosomal protein L34 can be suppressed by magnesium
Q92311624	Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo
Q57973932	Deficiency in the nuclear long noncoding RNA causes myogenic defects and heart remodeling in mice
Q92916364	Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer
Q36364631	Defining Genetic Fitness Determinants and Creating Genomic Resources for an Oral Pathogen
Q51415192	Defining Regulatory Elements in the Human Genome Using Nucleosome Occupancy and Methylome Sequencing (NOMe-Seq).
Q47148323	Defining the location of promoter-associated R-loops at near-nucleotide resolution using bisDRIP-seq.
Q93037439	Defining the transcription landscape of the Gram-negative marine bacterium Vibrio harveyi
Q35088957	Defining the transcriptomic landscape of Candida glabrata by RNA-Seq.
Q49527646	Delayed Degradation and Impaired Dendritic Delivery of Intron-Lacking EGFP-Arc/Arg3.1 mRNA in EGFP-Arc Transgenic Mice.
Q40369018	Deletion of 2.7 kb near HOXD3 in an Arabian horse with occipitoatlantoaxial malformation
Q90713678	Deletion of Gpr27 in vivo reduces insulin mRNA but does not result in diabetes
Q57295462	Deletions linked to PROG1 gene participate in plant architecture domestication in Asian and African rice
Q90341909	Delineating the role of MITF isoforms in pigmentation and tissue homeostasis
Q64890954	DeltaNp63-dependent super enhancers define molecular identity in pancreatic cancer by an interconnected transcription factor network.
Q40602521	Dependence-induced increase of alcohol self-administration and compulsive drinking mediated by the histone methyltransferase PRDM2.
Q38753118	Depletion of Mouse Cells from Human Tumor Xenografts Significantly Improves Downstream Analysis of Target Cells
Q37483972	Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
Q47686306	Derivation of ground-state female ES cells maintaining gamete-derived DNA methylation
Q116672799	Description and molecular characterisation of Pelecitus copsychi Uni, Mat Udin & Martin n. sp. (Nematoda: Onchocercidae) from the white-rumped shama Copsychus malabaricus (Scopoli) (Passeriformes: Muscicapidae) of Pahang, Malaysia
Q58795187	Description of Genetic Variants in Genes in Mexican Patients with Ovarian Cancer: A First Step towards Implementing Personalized Medicine
Q27334010	Descriptive Epidemiology and Whole Genome Sequencing Analysis for an Outbreak of Bovine Tuberculosis in Beef Cattle and White-Tailed Deer in Northwestern Minnesota
Q57170496	Design and MinION testing of a nanopore targeted gene sequencing panel for chronic lymphocytic leukemia
Q59352711	Design and validation of a universal influenza virus enrichment probe set and its utility in deep sequence analysis of primary cloacal swab surveillance samples of wild birds
Q37234566	Design of Effective Primary MicroRNA Mimics With Different Basal Stem Conformations.
Q37034262	Detailed Characterization of Human Induced Pluripotent Stem Cells Manufactured for Therapeutic Applications.
Q88182715	Detailed genomic characterization identifies high heterogeneity and histotype-specific genomic profiles in adrenocortical carcinomas
Q64968835	Detecting and Tracking Circulating Tumour DNA Copy Number Profiles during First Line Chemotherapy in Oesophagogastric Adenocarcinoma.
Q35032007	Detecting somatic genetic alterations in tumor specimens by exon capture and massively parallel sequencing.
Q93009797	Detection of CSF1 rearrangements deleting the 3' UTR in tenosynovial giant cell tumors
Q38666285	Detection of Differential DNA Methylation Under Stress Conditions Using Bisulfite Sequence Analysis.
Q47956458	Detection of EGFRvIII mutant DNA in the peripheral blood of brain tumor patients
Q92493499	Detection of Epstein-Barr Virus Infection in Non-Small Cell Lung Cancer
Q64059913	Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application
Q37709234	Detection of circulating tumor DNA in patients with advanced non-small cell lung cancer
Q90640909	Detection of circulating tumor cell DNA for monitoring advanced gastric cancer
Q100736938	Detection of early stage pancreatic cancer using 5-hydroxymethylcytosine signatures in circulating cell free DNA
Q56980521	Detection of mixed-strain infections by FACS and ultra-low input genome sequencing
Q35826206	Detection of murine leukemia virus in the Epstein-Barr virus-positive human B-cell line JY, using a computational RNA-Seq-based exogenous agent detection pipeline, PARSES.
Q47157939	Detection of tumor-derived DNA dispersed in the airway improves the diagnostic accuracy of bronchoscopy for lung cancer
Q64102415	Determination of local chromatin interactions using a combined CRISPR and peroxidase APEX2 system
Q97418674	Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third
Q44024204	Determining long-range chromatin interactions for selected genomic sites using 4C-seq technology: from fixation to computation.
Q64276102	Development and evaluation of a milk protein transcript depletion method for differential transcriptome analysis in mammary gland tissue
Q37666821	Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment
Q47137127	Development and validation of a targeted next generation DNA sequencing panel outperforming whole exome sequencing for the identification of clinically relevant genetic variants
Q36701360	Development and validation of allele-specific SNP/indel markers for eight yield-enhancing genes using whole-genome sequencing strategy to increase yield potential of rice, Oryza sativa L
Q34582256	Development of SNP markers identifying European wildcats, domestic cats, and their admixed progeny
Q49296229	Development of a Method to Implement Whole-Genome Bisulfite Sequencing of cfDNA from Cancer Patients and a Mouse Tumor Model.
Q35715337	Development of a Model System for Tick-Borne Flavivirus Persistence in HEK 293T Cells
Q89511089	Development of a Precision Medicine Workflow in Hematological Cancers, Aalborg University Hospital, Denmark
Q92794867	Development of a Versatile, Near Full Genome Amplification and Sequencing Approach for a Broad Variety of HIV-1 Group M Variants
Q35182386	Development of molecular markers tightly linked to Pvr4 gene in pepper using next-generation sequencing.
Q28655705	Development of synchronous VHL syndrome tumors reveals contingencies and constraints to tumor evolution
Q98394771	Developmental changes in the accessible chromatin, transcriptome and Ascl1-binding correlate with the loss in Müller Glial regenerative potential
Q37457271	Developmentally programmed germ cell remodelling by endodermal cell cannibalism
Q36170468	Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis
Q37558643	Diagnosis of Noonan syndrome and related disorders using target next generation sequencing
Q39275885	Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing
Q36503498	Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing
Q36019509	Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome
Q34734645	Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 Genes
Q90484210	Diagnostic Utility of Next-Generation Sequencing for Disorders of Somatic Mosaicism: A Five-Year Cumulative Cohort
Q41783629	Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors
Q57899034	Diagnostic applications of next generation sequencing: working towards quality standards/Diagnostische Anwendung von Next Generation Sequencing: Auf dem Weg zu Qualitätsstandards
Q48825369	Diagnostic exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis.
Q53794596	Diagnostic use of computational retrotransposon detection: Successful definition of pathogenetic mechanism in a ciliopathy phenotype.
Q36751630	Dicer-independent RNA-directed DNA methylation in Arabidopsis
Q98223004	Dichotomous engagement of HDAC3 activity governs inflammatory responses
Q34993956	Differences in DNA methylation between human neuronal and glial cells are concentrated in enhancers and non-CpG sites
Q34720273	Differences in gastric carcinoma microenvironment stratify according to EBV infection intensity: implications for possible immune adjuvant therapy
Q53824357	Different chromatin and DNA sequence characteristics define glucocorticoid receptor binding sites that are blocked or not blocked by coregulator Hic-5.
Q48157894	Different milk diets have substantial effects on the jejunal mucosal immune system of pre-weaning calves, as demonstrated by whole transcriptome sequencing.
Q42797675	Different molecular complexes that mediate transcriptional induction and repression by FoxP3.
Q50098941	Different mutational function of low- and high-linear energy transfer heavy-ion irradiation demonstrated by whole-genome resequencing of Arabidopsis mutants.
Q90616770	Differential Modulation of Innate Immune Responses in Human Primary Cells by Influenza A Viruses Carrying Human or Avian Nonstructural Protein 1
Q39002288	Differential expression of microRNAs and potential targets under drought stress in barley.
Q40138268	Differential expression of novel microRNAs in response to the infection of a TMV mutant with an internal poly(A) tract in N. benthamiana
Q34504665	Differential expression of small RNAs under chemical stress and fed-batch fermentation in E. coli
Q24633890	Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
Q90556071	Differential modulation of the androgen receptor for prostate cancer therapy depends on the DNA response element
Q33662656	Differential regulation of the α-globin locus by Krüppel-like Factor 3 in erythroid and non-erythroid cells
Q34723952	Differential transcript isoform usage pre- and post-zygotic genome activation in zebrafish
Q37231038	Differential urinary specific gravity as a molecular phenotype of the bladder cancer genetic association in the urea transporter gene, SLC14A1.
Q98286423	Differentiating Drosophila female germ cells initiate Polycomb silencing by regulating PRC2-interacting proteins
Q91341516	Differentiation of human pluripotent stem cells into neurons or cortical organoids requires transcriptional co-regulation by UTX and 53BP1
Q33557596	Different enhancer classes in Drosophila bind distinct architectural proteins and mediate unique chromatin interactions and 3D architecture
Q37482702	Digenic mutations of human OCRL paralogs in Dent's disease type 2 associated with Chiari I malformation
Q38911544	Digenome-seq: genome-wide profiling of CRISPR-Cas9 off-target effects in human cells
Q38364793	Digital Sorting of Pure Cell Populations Enables Unambiguous Genetic Analysis of Heterogeneous Formalin-Fixed Paraffin-Embedded Tumors by Next Generation Sequencing
Q34044207	Dimeric CRISPR RNA-Guided FokI-dCas9 Nucleases Directed by Truncated gRNAs for Highly Specific Genome Editing
Q61795989	Direct RNA sequencing on nanopore arrays redefines the transcriptional complexity of a viral pathogen
Q57153482	Direct estimation of the spontaneous mutation rate by short-term mutation accumulation lines in
Q99350319	Direct identification of a mutation in OsSh1 causing non-shattering in a rice (Oryza sativa L.) mutant cultivar using whole-genome resequencing
Q100395284	Direct interactions with commensal streptococci modify intercellular communication behaviors of Streptococcus mutans
Q41101126	Direct interrogation of the role of H3K9 in metazoan heterochromatin function.
Q41620118	Direct links between the vernalization response and other key traits of cereal crops
Q33741464	Direct observation of genomic heterogeneity through local haplotyping analysis
Q35823718	Direct, genome-wide assessment of DNA mutations in single cells.
Q57030878	Direct-to-consumer DNA testing of 6,000 dogs reveals 98.6-kb duplication associated with blue eyes and heterochromia in Siberian Huskies
Q90287172	Directed Nucleosome Sliding during the Formation of the Simian Virus 40 Particle Exposes DNA Sequences Required for Early Transcription
Q36817901	Directing an artificial zinc finger protein to new targets by fusion to a non-DNA-binding domain
Q61794394	Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma
Q34756561	Discovering motifs that induce sequencing errors
Q36522778	Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology
Q37615837	Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Q37609524	Discovery of Cancer Driver Long Noncoding RNAs across 1112 Tumour Genomes: New Candidates and Distinguishing Features
Q90327712	Discovery of Novel Sequences in 1,000 Swedish Genomes
Q89502964	Discovery of a New TLR Gene and Gene Expansion Event through Improved Desert Tortoise Genome Assembly with Chromosome-Scale Scaffolds
Q87900070	Discovery of a new predominant cytosine DNA modification that is linked to gene expression in malaria parasites.
Q34107765	Discovery of common sequences absent in the human reference genome using pooled samples from next generation sequencing
Q101226308	Discovery of driver non-coding splice-site-creating mutations in cancer
Q41086738	Discovery of ethanol-responsive small RNAs in Zymomonas mobilis
Q47209586	Discovery of internalizing antibodies to basal breast cancer cells
Q57464842	Discovery of potential causative mutations in human coding and noncoding genome with the interactive software BasePlayer
Q92954866	Discrimination of low- and high-grade appendiceal mucinous neoplasms by targeted sequencing of cancer-related variants
Q41625772	Disease-stabilizing treatment based on all-trans retinoic acid and valproic acid in acute myeloid leukemia - identification of responders by gene expression profiling of pretreatment leukemic cells
Q87014664	Dismantling papillary renal cell carcinoma classification: The heterogeneity of genetic profiles suggests several independent diseases
Q91792286	Disruption of Broad Epigenetic Domains in PDAC Cells by HAT Inhibitors
Q33756974	Disruption of Mycobacterium avium subsp. paratuberculosis-specific genes impairs in vivo fitness
Q97547609	Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype
Q64057851	Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability
Q96577087	Dissecting myogenin-mediated retinoid X receptor signaling in myogenic differentiation
Q51418242	Dissecting super-enhancer hierarchy based on chromatin interactions.
Q89893370	Dissecting the Regulatory Strategies of NF-κB RelA Target Genes in the Inflammatory Response Reveals Differential Transactivation Logics
Q37631820	Dissecting the chromatin interactome of microRNA genes.
Q37701311	Dissecting the function of the adult β-globin downstream promoter region using an artificial zinc finger DNA-binding domain
Q90114569	Distinct Classes of Chromatin Loops Revealed by Deletion of an RNA-Binding Region in CTCF
Q64272858	Distinct Gut Virome Profile of Pregnant Women With Type 1 Diabetes in the ENDIA Study
Q89831609	Distinct Mesenchymal Cell Populations Generate the Essential Intestinal BMP Signaling Gradient
Q46293907	Distinct Trajectories of Massive Recent Gene Gains and Losses in Populations of a Microbial Eukaryotic Pathogen
Q36189980	Distinct features of lamin A-interacting chromatin domains mapped by ChIP-sequencing from sonicated or micrococcal nuclease-digested chromatin
Q48701324	Distinct genetic profiles of extracranial and intracranial acral melanoma metastases.
Q35476240	Distinguishing between productive and abortive promoters using a random forest classifier in Mycoplasma pneumoniae
Q21092704	Distributive conjugal transfer in mycobacteria generates progeny with meiotic-like genome-wide mosaicism, allowing mapping of a mating identity locus
Q89888262	Disturbance of floral colour pattern by activation of an endogenous pararetrovirus, petunia vein clearing virus, in aged petunia plants
Q41068482	Div-Seq: Single-nucleus RNA-Seq reveals dynamics of rare adult newborn neurons
Q53730678	Diverse BRCA1 and BRCA2 Reversion Mutations in Circulating Cell-Free DNA of Therapy-Resistant Breast or Ovarian Cancer.
Q37683831	Diverse origin of mitochondrial lineages in Iron Age Black Sea Scythians
Q92048552	DolphinNext: a distributed data processing platform for high throughput genomics
Q92538893	Domestication of previously uncultivated Candidatus Desulforudis audaxviator from a deep aquifer in Siberia sheds light on its physiology and evolution
Q36116699	Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia
Q64098975	Dorsal-Ventral Differences in Neural Stem Cell Quiescence Are Induced by p57KIP2/Dacapo
Q60310169	Downregulation of ERG and FLI1 expression in endothelial cells triggers endothelial-to-mesenchymal transition
Q36842582	Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Q50036364	Draft Genome Sequence of Burkholderia sp. Strain WAC0059, a Bacterium Isolated from the Medicinal Fungus Antrodia cinnamomea.
Q36381837	Draft Genome Sequence of Pedobacter sp. Strain Hv1, an Isolate from Medicinal Leech Mucosal Castings
Q60550871	Draft Genome Sequence of Vibrio vulnificus 86573B, a Bacterium Isolated from Diseased Tilapia in Taiwan
Q36323237	Draft Genome Sequence of a 16SrII-A Subgroup Phytoplasma Associated with Purple Coneflower (Echinacea purpurea) Witches' Broom Disease in Taiwan
Q90278143	Driver gene alterations and activated signaling pathways toward malignant progression of gastrointestinal stromal tumors
Q55004535	Drosophila Larval Brain Neoplasms Present Tumour-Type Dependent Genome Instability.
Q95305911	Drosophila SWR1 and NuA4 complexes are defined by DOMINO isoforms
Q90730210	Drug-induced chromatin accessibility changes associate with sensitivity to liver tumor promotion
Q97069606	Dual RNA-seq of Orientia tsutsugamushi informs on host-pathogen interactions for this neglected intracellular human pathogen
Q47284112	Dual Targeting of Oncogenic Activation and Inflammatory Signaling Increases Therapeutic Efficacy in Myeloproliferative Neoplasms.
Q28533839	Dual analysis of the murine cytomegalovirus and host cell transcriptomes reveal new aspects of the virus-host cell interface
Q37346983	Dual chromatin recognition by the histone deacetylase complex HCHC is required for proper DNA methylation in Neurospora crassa
Q94466529	Dual histone methyl reader ZCWPW1 facilitates repair of meiotic double strand breaks in male mice
Q55337080	Dual origin of relapses in retinoic-acid resistant acute promyelocytic leukemia.
Q92150346	Dual-targeting strategy using trastuzumab and lapatinib in a patient with HER2 gene amplification in recurrent metachronous metastatic gallbladder carcinoma
Q38633192	Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus.
Q64234454	Duplication of F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma
Q36177380	Dwarfism with joint laxity in Friesian horses is associated with a splice site mutation in B4GALT7.
Q90266119	Dynamic Changes in Genome-Wide Histone3 Lysine27 Trimethylation and Gene Expression of Soybean Roots in Response to Salt Stress
Q34453834	Dynamic DNA methylation orchestrates cardiomyocyte development, maturation and disease.
Q51839827	Dynamic Reorganization of Chromatin Accessibility Signatures during Dedifferentiation of Secretory Precursors into Lgr5+ Intestinal Stem Cells.
Q59350055	Dynamic Transcriptome Profiling Dataset of Vaccinia Virus Obtained from Long-read Sequencing Techniques
Q92496123	Dynamic and regulated TAF gene expression during mouse embryonic germ cell development
Q34596224	Dynamic changes in the Streptococcus pneumoniae transcriptome during transition from biofilm formation to invasive disease upon influenza A virus infection
Q37400379	Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
Q34179675	Dynamic microRNA gene transcription and processing during T cell development.
Q93223071	Dynamic molecular monitoring reveals that SWI-SNF mutations mediate resistance to ibrutinib plus venetoclax in mantle cell lymphoma
Q33742601	Dynamic regulation of genome-wide pre-mRNA splicing and stress tolerance by the Sm-like protein LSm5 in Arabidopsis
Q38466295	Dynamic transition of transcription and chromatin landscape during fission yeast adaptation to glucose starvation.
Q90468424	Dynamics and genomic landscape of CD8+ T cells undergoing hepatic priming
Q52716666	Dynamics of sister chromatid resolution during cell cycle progression.
Q35152112	Dysregulation of X chromosome inactivation in high grade ovarian serous adenocarcinoma
Q97419111	Dysregulation of cancer genes by recurrent intergenic fusions
Q50062541	EAT1 transcription factor, a non-cell-autonomous regulator of pollen production, activates meiotic small RNA biogenesis in rice anther tapetum.
Q33591193	EED orchestration of heart maturation through interaction with HDACs is H3K27me3-independent.
Q41472663	EGFR G796D mutation mediates resistance to osimertinib
Q36506742	EHMT2 directs DNA methylation for efficient gene silencing in mouse embryos
Q42365224	EIN2 mediates direct regulation of histone acetylation in the ethylene response
Q37338872	EIN2-dependent regulation of acetylation of histone H3K14 and non-canonical histone H3K23 in ethylene signalling.
Q38925517	ELF-MF exposure affects the robustness of epigenetic programming during granulopoiesis
Q94460607	EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
Q58786329	EMBLmyGFF3: a converter facilitating genome annotation submission to European Nucleotide Archive
Q24600461	ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19
Q27852637	ESR1 ligand-binding domain mutations in hormone-resistant breast cancer
Q38696706	ETV4 and AP1 Transcription Factors Form Multivalent Interactions with three Sites on the MED25 Activator-Interacting Domain
Q38844207	ETV6/RUNX1-like acute lymphoblastic leukemia: A novel B-cell precursor leukemia subtype associated with the CD27/CD44 immunophenotype.
Q39371111	EXPLoRA-web: linkage analysis of quantitative trait loci using bulk segregant analysis
Q28741454	EZH2 codon 641 mutations are common in BCL2-rearranged germinal center B cell lymphomas
Q92668386	Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth
Q89769213	Early detection of lysosomal diseases by screening of cases of idiopathic splenomegaly and/or thrombocytopenia with a next-generation sequencing gene panel
Q47820852	Early life stress confers lifelong stress susceptibility in mice via ventral tegmental area OTX2.
Q50668042	Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair.
Q41517895	Ecological and genetic interactions between cyanobacteria and viruses in a low-oxygen mat community inferred through metagenomics and metatranscriptomics.
Q41658107	Editor's Highlight: Neonatal Activation of the Xenobiotic-Sensors PXR and CAR Results in Acute and Persistent Down-regulation of PPARα-Signaling in Mouse Liver
Q60307202	Effect of Upregulated DNA Replication and Sister Chromatid Cohesion 1 Expression on Proliferation and Prognosis in Hepatocellular Carcinoma
Q90281664	Effect of diversity in gp41 membrane proximal external region of primary HIV-1 Indian subtype C sequences on interaction with broadly neutralizing antibodies 4E10 and 10E8
Q91620199	Effect of low-level BCR-ABL1 kinase domain mutations identified by next-generation sequencing in patients with chronic myeloid leukaemia: a population-based study
Q48252015	Effect of plasmid design and type of integration event on recombinant protein expression in Pichia pastoris
Q58702354	Effects of maternal nutrition on the expression of genomic imprinted genes in ovine fetuses
Q31064721	Effects of the Ion PGM™ Hi-Q™ sequencing chemistry on sequence data quality
Q89236313	Effects of the stimuli-dependent enrichment of 8-oxoguanine DNA glycosylase1 on chromatinized DNA
Q34341329	Efficiency and power as a function of sequence coverage, SNP array density, and imputation
Q64901933	Efficient Epstein-Barr Virus Progeny Production Mediated by Cancer-Derived LMP1 and Virally-Encoded microRNAs.
Q55102445	Efficient Expression of Genes in the Drosophila Germline Using a UAS Promoter Free of Interference by Hsp70 piRNAs.
Q36189031	Efficient Preparation of High-Complexity ChIP-Seq Profiles from Early Xenopus Embryos.
Q98945954	Efficient chromatin profiling of H3K4me3 modification in cotton using CUT&Tag
Q30357150	Efficient mapping of transgene integration sites and local structural changes in Cre transgenic mice using targeted locus amplification.
Q100311082	Elements at the 5' end of Xist harbor SPEN-independent transcriptional antiterminator activity
Q92395095	Elucidation of de novo small insertion/deletion biology with parent-of-origin phasing
Q30401330	Emergence and Evolution of Multidrug-Resistant Klebsiella pneumoniae with both blaKPC and blaCTX-M Integrated in Chromosome
Q92542205	Endodermal Maternal Transcription Factors Establish Super-Enhancers during Zygotic Genome Activation
Q90465700	Endogenous epitope-tagging of Tet1, Tet2 and Tet3 identifies TET2 as a naïve pluripotency marker
Q99207799	Endogenous retroviruses drive species-specific germline transcriptomes in mammals
Q90604753	Endometrial Carcinomas with a "Serous" Component in Young Women are Enriched for DNA Mismatch Repair Deficiency, Lynch Syndrome, and POLE Exonuclease Domain Mutations
Q90697824	Endometrial cancer with an EML4-ALK rearrangement
Q38695836	Endothelial protein C receptor is overexpressed in colorectal cancer as a result of amplification and hypomethylation of chromosome 20q
Q89748615	Engineering bacterial symbionts of nematodes improves biocontrol potential of the western corn rootworm
Q64448282	Enhanced Growth of Pilin-Deficient Geobacter sulfurreducens Mutants in Carbon Poor and Electron Donor Limiting Conditions
Q55088118	Enhanced JBrowse plugins for epigenomics data visualization.
Q47633059	Enhanced Nociception in Angelman Syndrome Model Mice
Q48194067	Enhanced Wort Fermentation with De Novo Lager Hybrids Adapted to High-Ethanol Environments
Q64101032	Enhanced and controlled chromatin extraction from FFPE tissues and the application to ChIP-seq
Q38263926	Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
Q30382864	Enhanced whole exome sequencing by higher DNA insert lengths.
Q92915904	Enhancement of LIN28B-induced hematopoietic reprogramming by IGF2BP3
Q61124893	Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands
Q89093847	Enhancer of zeste homolog 2 (Ezh2) controls bone formation and cell cycle progression during osteogenesis in mice
Q102220255	Enhancer remodeling promotes tumor-initiating activity in NRF2-activated non-small cell lung cancers
Q58114043	Enhancer, transcriptional, and cell fate plasticity precedes intestinal determination during endoderm development
Q35097959	Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain
Q64937259	Enhancing face validity of mouse models of Alzheimer's disease with natural genetic variation.
Q110949953	Enhort: a platform for deep analysis of genomic positions
Q41001736	Enriched domain detector: a program for detection of wide genomic enrichment domains robust against local variations
Q38635837	Enrichment by hybridisation of long DNA fragments for Nanopore sequencing
Q36012704	Enrichment of H3K9me2 on Unsynapsed Chromatin in Caenorhabditis elegans Does Not Target de Novo Sites
Q46441245	Entire nucleotide sequences of Gossypium raimondii and G. arboreum mitochondrial genomes revealed A-genome species as cytoplasmic donor of the allotetraploid species.
Q90240003	Environmentally induced plasticity of programmed DNA elimination boosts somatic variability in Paramecium tetraurelia
Q36776051	Enzootic Arbovirus Surveillance in Forest Habitat and Phylogenetic Characterization of Novel Isolates of Gamboa Virus in Panama
Q96303513	Eosinophil function in adipose tissue is regulated by Krüppel-like factor 3 (KLF3)
Q35879513	Epigenetic Alterations in Density Selected Human Spermatozoa for Assisted Reproduction
Q90376437	Epigenetic Changes Associated with Early Life Experiences: Saliva, A Biospecimen for DNA Methylation Signatures
Q36258923	Epigenetic Landscape of Kaposi's Sarcoma-Associated Herpesvirus Genome in Classic Kaposi's Sarcoma Tissues
Q46890724	Epigenetic Regulation of ZBTB18 Promotes Glioblastoma Progression.
Q46789737	Epigenetic Regulation of the Sex Determination Gene MeGI in Polyploid Persimmon
Q36626342	Epigenetic Studies Point to DNA Replication/Repair Genes as a Basis for the Heritable Nature of Long Term Complications in Diabetes
Q49985254	Epigenetic alterations in TRAMP mice: epigenome DNA methylation profiling using MeDIP-seq.
Q64065013	Epigenetic and transcriptional profiling of triple negative breast cancer
Q41641943	Epigenetic changes in T-cell and monocyte signatures and production of neurotoxic cytokines in ALS patients
Q55008852	Epigenetic drift of H3K27me3 in aging links glycolysis to healthy longevity in Drosophila.
Q64086806	Epigenetic drug library screening identified an LSD1 inhibitor to target UTX-deficient cells for differentiation therapy
Q46302040	Epigenetic mechanisms underlying maternal diabetes-associated risk of congenital heart disease.
Q92460255	Epigenetic priming by Dot1l in lymphatic endothelial progenitors ensures normal lymphatic development and function
Q39025220	Epigenetic regulation of GATA2 and its impact on normal karyotype acute myeloid leukemia.
Q47664340	Epigenetic regulation of gene expression in cancer: techniques, resources and analysis.
Q35211627	Epigenetic regulation of the ELOVL6 gene is associated with a major QTL effect on fatty acid composition in pigs.
Q64286874	Epigenetically modulated FOXM1 suppresses dendritic cell maturation in pancreatic cancer and colon cancer
Q37733832	Epigenetically-driven anatomical diversity of synovial fibroblasts guides joint-specific fibroblast functions.
Q39117081	Epigenetics and Control of RNAs
Q92570048	Epigenome Mapping Identifies Tumor-Specific Gene Expression in Primary Rectal Cancer
Q37721730	Epigenome mapping highlights chromatin-mediated gene regulation in the protozoan parasite Trichomonas vaginalis.
Q38602034	Epigenome-wide analysis of DNA methylation in lung tissue shows concordance with blood studies and identifies tobacco smoke-inducible enhancers
Q38808095	Epigenome-wide effects of vitamin D and their impact on the transcriptome of human monocytes involve CTCF.
Q90261216	Epigenomic Profiling Discovers Trans-lineage SOX2 Partnerships Driving Tumor Heterogeneity in Lung Squamous Cell Carcinoma
Q36367191	Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells
Q40357382	Epigenomic landscape of 5-hydroxymethylcytosine reveals its transcriptional regulation of lncRNAs in colorectal cancer.
Q57295433	Epigenomic map of human liver reveals principles of zonated morphogenic and metabolic control
Q45325680	Epistastic interactions within the Junín virus envelope glycoprotein complex provide an evolutionary barrier to reversion in the live-attenuated Candid#1 vaccine
Q33630385	Epistatic and allelic interactions control expression of ribosomal RNA gene clusters in Arabidopsis thaliana
Q42776260	Epithelial-Mesenchymal Micro-niches Govern Stem Cell Lineage Choices
Q92499172	Epitranscriptomic profiling in human placenta: N6-methyladenosine modification at the 5'-untranslated region is related to fetal growth and preeclampsia
Q96958671	Epiviz File Server: Query, Transform and Interactively Explore Data from Indexed Genomic Files
Q56895076	Epiviz Web Components: reusable and extensible component library to visualize functional genomic datasets
Q28608051	Epiviz: a view inside the design of an integrated visual analysis software for genomics
Q38730271	Epo reprograms the epigenome of erythroid cells
Q37336454	Epstein-Barr virus and human herpesvirus 6 detection in a non-Hodgkin's diffuse large B-cell lymphoma cohort by using RNA sequencing
Q37493384	Epstein-Barr virus super-enhancer eRNAs are essential for MYC oncogene expression and lymphoblast proliferation
Q34044076	Essential Genes in the Core Genome of the Human Pathogen Streptococcus pyogenes
Q58705671	Essential Nucleoid Associated Protein mIHF (Rv1388) Controls Virulence and Housekeeping Genes in Mycobacterium tuberculosis
Q41863092	Essential requirements for the detection and degradation of invaders by the Haloferax volcanii CRISPR/Cas system I-B.
Q41134756	Establishing the origin of metastatic deposits in the setting of multiple primary malignancies: the role of massively parallel sequencing
Q92130629	Establishment and characterization of a cell line and patient-derived xenograft (PDX) from peritoneal metastasis of low-grade serous ovarian carcinoma
Q28485145	Establishment and characterization of a highly tumourigenic and cancer stem cell enriched pancreatic cancer cell line as a well defined model system
Q92804245	Establishment of an eHAP1 human haploid cell line hybrid reference genome assembled from short and long reads
Q61796499	Establishment, molecular and biological characterization of HCB-514: a novel human cervical cancer cell line
Q99710555	Estimation of the SNP Mutation Rate in Two Vegetatively Propagating Species of Duckweed
Q30407671	Estrogen modulation of endosome-associated toll-like receptor 8: an IFNα-independent mechanism of sex-bias in systemic lupus erythematosus.
Q37085951	Estrogen receptor alpha (ERα/ESR1) mediates the p53-independent overexpression of MDM4/MDMX and MDM2 in human breast cancer
Q38723501	Estrogen-regulated STAT1 activation promotes TLR8 expression to facilitate signaling via microRNA-21 in systemic lupus erythematosus.
Q64122242	Ets1 suppresses atopic dermatitis by suppressing pathogenic T cell responses
Q36289245	Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
Q37025950	Evaluating cell lines as tumour models by comparison of genomic profiles
Q38909912	Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number Variants.
Q50050350	Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
Q89522036	Evaluating the genome and resistome of extensively drug-resistant Klebsiella pneumoniae using native DNA and RNA Nanopore sequencing
Q33839369	Evaluation and optimisation of indel detection workflows for ion torrent sequencing of the BRCA1 and BRCA2 genes
Q46211586	Evaluation and rational design of guide RNAs for efficient CRISPR/Cas9-mediated mutagenesis in Ciona
Q35674525	Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing
Q36367163	Evaluation of MC1R high-throughput nucleotide sequencing data generated by the 1000 Genomes Project
Q35757609	Evaluation of Unbiased Next-Generation Sequencing of RNA (RNA-seq) as a Diagnostic Method in Influenza Virus-Positive Respiratory Samples.
Q38662565	Evaluation of exome variants using the Ion Proton Platform to sequence error-prone regions
Q37131995	Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM)
Q90681451	Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton
Q36055662	EventPointer: an effective identification of alternative splicing events using junction arrays.
Q100560062	Evidence for 28 genetic disorders discovered by combining healthcare and research data
Q64063635	Evidence for DNA-mediated nuclear compartmentalization distinct from phase separation
Q37291373	Evidence for Direct Control of Virulence and Defense Gene Circuits by the Pseudomonas aeruginosa Quorum Sensing Regulator, MvfR
Q55108557	Evidence for Mitochondrial Genome Methylation in the Yeast Candida albicans: A Potential Novel Epigenetic Mechanism Affecting Adaptation and Pathogenicity?
Q43741099	Evidence for regulation of columnar habit in apple by a putative 2OG-Fe(II) oxygenase
Q46495792	Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi.
Q34277284	Evolution of Burkholderia pseudomallei in recurrent melioidosis
Q98288781	Evolution of Multi-Resistance to Vancomycin, Daptomycin, and Linezolid in Methicillin-Resistant Staphylococcus aureus Causing Persistent Bacteremia
Q104064794	Evolution of Pseudomonas aeruginosa toward higher fitness under standard laboratory conditions
Q83229014	Evolution of Yin and Yang isoforms of a chromatin remodeling subunit precedes the creation of two genes
Q37212864	Evolution of a FLT3-TKD mutated subclone at meningeal relapse in acute promyelocytic leukemia
Q53725145	Evolution of cross-resistance to medical triazoles in Aspergillus fumigatus through selection pressure of environmental fungicides.
Q21090479	Evolution of genome size and complexity in the rhabdoviridae
Q101116526	Evolution of resistance to fluoroquinolones by dengue virus serotype 4 provides insight into mechanism of action and consequences for viral fitness
Q89702162	Evolution of self-compatibility by a mutant Sm-RNase in citrus
Q47148265	Evolution of sequence-specific anti-silencing systems in Arabidopsis.
Q46301564	Evolution of the alternative AQP2 gene: Acquisition of a novel protein-coding sequence in dolphins
Q35529883	Evolutionary Engineering Improves Tolerance for Replacement Jet Fuels in Saccharomyces cerevisiae
Q38693643	Evolutionary adaptation revealed by comparative genome analysis of woolly mammoths and elephants
Q64903822	Evolutionary analysis of human parechovirus type 3 and clinical outcomes of infection during the 2017-18 Australian epidemic.
Q35700941	Evolutionary engineering of a wine yeast strain revealed a key role of inositol and mannoprotein metabolism during low-temperature fermentation
Q28646150	Evolutionary insights from de novo transcriptome assembly and SNP discovery in California white oaks
Q90186568	Evolutionary repair: Changes in multiple functional modules allow meiotic cohesin to support mitosis
Q100416601	Evolutionary trajectory of fish Piscine novirhabdovirus (=Viral Hemorrhagic Septicemia Virus) across its Laurentian Great Lakes history: Spatial and temporal diversification
Q36499949	Evolved hexose transporter enhances xylose uptake and glucose/xylose co-utilization in Saccharomyces cerevisiae.
Q47791066	Ex-vivo assessment of drug response on breast cancer primary tissue with preserved microenvironments
Q35745210	ExScalibur: A High-Performance Cloud-Enabled Suite for Whole Exome Germline and Somatic Mutation Identification
Q46744224	Examining the Causes and Consequences of Context-Specific Differential DNA Methylation in Maize.
Q57281823	Examining the contribution of smoking and HPV towards the etiology of oral cavity squamous cell carcinoma using high-throughput sequencing: A prospective observational study
Q58782636	Examining transcriptional changes to DNA replication and repair factors over uveal melanoma subtypes
Q64097541	Excessive miR-25-3p maturation via N-methyladenosine stimulated by cigarette smoke promotes pancreatic cancer progression
Q91081542	Excised linear introns regulate growth in yeast
Q36143956	Exclusion of the 750-kb genetically unstable region at Xq27 as a candidate locus for prostate malignancy in HPCX1-linked families.
Q59350377	Existing host range mutations constrain further emergence of RNA viruses
Q93103710	Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium
Q37678950	Exome Sequencing Identifies Potentially Druggable Mutations in Nasopharyngeal Carcinoma.
Q35897454	Exome analysis of a family with pleiotropic congenital heart disease.
Q34542441	Exome capture sequencing of adenoma reveals genetic alterations in multiple cellular pathways at the early stage of colorectal tumorigenesis
Q35943473	Exome screening to identify loss-of-function mutations in the rhesus macaque for development of preclinical models of human disease
Q27027055	Exome sequencing and complex disease: practical aspects of rare variant association studies
Q39314513	Exome sequencing and digital PCR analyses reveal novel mutated genes related to the metastasis of pancreatic ductal adenocarcinoma
Q34219041	Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus
Q34408752	Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer
Q24314885	Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
Q30362427	Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family.
Q50538593	Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
Q24616117	Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer
Q92611050	Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations
Q42245258	Exome sequencing of extreme clopidogrel response phenotypes identifies B4GALT2 as a determinant of on-treatment platelet reactivity
Q91521978	Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
Q39290981	Exome sequencing of hepatitis B virus-associated hepatocellular carcinoma
Q34474029	Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences
Q28254930	Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease
Q30426901	Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families
Q36346537	Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders
Q30617099	Exome-based analysis for RNA epigenome sequencing data
Q34535838	Exon Junction Complexes Show a Distributional Bias toward Alternatively Spliced mRNAs and against mRNAs Coding for Ribosomal Proteins.
Q91204025	Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies
Q37710155	Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing
Q33877449	Experimental Evolution Reveals Favored Adaptive Routes to Cell Aggregation in Yeast
Q33923485	Experimental and Computational Considerations in the Study of RNA-Binding Protein-RNA Interactions
Q90003241	Expert curation of the human and mouse olfactory receptor gene repertoires identifies conserved coding regions split across two exons
Q45058251	Exploiting AR-Regulated Drug Transport to Induce Sensitivity to the Survivin Inhibitor YM155.
Q33575864	Exploiting the extraordinary genetic polymorphism of ciona for developmental genetics with whole genome sequencing
Q36288788	Exploratory bioinformatics investigation reveals importance of "junk" DNA in early embryo development
Q64985785	Exploring Genetic Data Across Individuals: Design and Evaluation of a Novel Comparative Report Tool.
Q98730664	Exploring Non-Coding RNAs in RNAcentral
Q90888062	Exploring a Pool-seq-only approach for gaining population genomic insights in nonmodel species
Q36120489	Exploring and visualizing multidimensional data in translational research platforms.
Q98572015	Exploring the virulence gene interactome with CRISPR/dCas9 in the human malaria parasite
Q57485144	Exposed to Sublethal Levels of Hydrogen Peroxide Mounts a Complex Transcriptional Response
Q48120379	Expression analysis of candidate genes for fatty acid composition in adipose tissue and identification of regulatory regions
Q31132409	Expression and methylation data from SLE patient and healthy control blood samples subdivided with respect to ARID3a levels
Q39090019	Expression of a non-coding RNA in ectromelia virus is required for normal plaque formation.
Q100415826	Expression of fatty acid and triacylglycerol synthesis genes in interspecific hybrids of oil palm
Q35608982	Expression of heterologous sigma factors enables functional screening of metagenomic and heterologous genomic libraries
Q38727204	Expression of the Antisense-to-Latency Transcript Long Noncoding RNA in Kaposi's Sarcoma-Associated Herpesvirus
Q36380247	Expression profile of Epstein-Barr virus and human adenovirus small RNAs in tonsillar B and T lymphocytes
Q87606615	Expression profiling of snoRNAs in normal hematopoiesis and AML
Q33974147	ExpressionPlot: a web-based framework for analysis of RNA-Seq and microarray gene expression data
Q38799740	Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
Q92579102	Extensive Recovery of Embryonic Enhancer and Gene Memory Stored in Hypomethylated Enhancer DNA
Q59349577	Extensive editing of cellular and viral double-stranded RNA structures accounts for innate immunity suppression and the proviral activity of ADAR1p150
Q34325564	Extensive evolutionary changes in regulatory element activity during human origins are associated with altered gene expression and positive selection
Q87800507	Extraction of Molecular Features through Exome to Transcriptome Alignment
Q89161457	Extrapolation of Variant Phase in Mitochondrial Short-Chain Enoyl-CoA Hydratase (ECHS1) Deficiency
Q42209149	Extreme HOT regions are CpG-dense promoters in C. elegans and humans
Q38712800	Eye movement disorders are an early manifestation of CACNA1A mutations in children
Q83229853	FAK activity sustains intrinsic and acquired ovarian cancer resistance to platinum chemotherapy
Q37130034	FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly
Q38694309	FGFR2 Amplification in Colorectal Adenocarcinoma
Q36251989	FGFR2 mutation in 46,XY sex reversal with craniosynostosis
Q30503882	FISH Oracle: a web server for flexible visualization of DNA copy number data in a genomic context.
Q64971573	FNBtools: A Software to Identify Homozygous Lesions in Deletion Mutant Populations.
Q38781895	FOXA1 defines cancer cell specificity.
Q61799066	FOXM1 modulates 5-FU resistance in colorectal cancer through regulating TYMS expression
Q53081210	FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
Q91691711	FTO controls reversible m6Am RNA methylation during snRNA biogenesis
Q89568569	Factor 8 Gene Mutation Spectrum of 270 Patients with Haemophilia A: Identification of 36 Novel Mutations
Q58759684	Facultative dosage compensation of developmental genes on autosomes in Drosophila and mouse embryonic stem cells
Q90589943	Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families
Q57284117	Familial breast cancer and DNA repair genes: insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
Q41194940	Family genome browser: visualizing genomes with pedigree information.
Q36457608	Farewell to GBM-O: Genomic and transcriptomic profiling of glioblastoma with oligodendroglioma component reveals distinct molecular subgroups.
Q36265829	Fast and accurate mutation detection in whole genome sequences of multiple isogenic samples with IsoMut
Q34230237	Fast homozygosity mapping and identification of a zebrafish ENU-induced mutation by whole-genome sequencing
Q34989928	FastDMA: an infinium humanmethylation450 beadchip analyzer
Q50444877	Fat mass and obesity-associated (FTO) protein regulates adult neurogenesis.
Q64083862	Feasibility and utility of a panel testing for 114 cancer-associated genes in a clinical setting: A hospital-based study
Q39633438	Feedback Regulation of ABA Signaling and Biosynthesis by a bZIP Transcription Factor Targets Drought-Resistance-Related Genes.
Q37720599	Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate
Q92224189	Fibrogenic Activity of MECP2 Is Regulated by Phosphorylation in Hepatic Stellate Cells
Q36172253	Field monitoring of avian influenza viruses: whole-genome sequencing and tracking of neuraminidase evolution using 454 pyrosequencing
Q42444938	Fine mapping and chromosome walking towards the Ror1 locus in barley (Hordeum vulgare L.).
Q104486460	Fine mapping and identification of candidate genes for the peach powdery mildew resistance gene Vr3
Q34956008	Fine mapping of V(D)J recombinase mediated rearrangements in human lymphoid malignancies
Q36168180	Fine mapping of a QTL on bovine chromosome 6 using imputed full sequence data suggests a key role for the group-specific component (GC) gene in clinical mastitis and milk production.
Q90258065	Fine-Grained Analysis of Spontaneous Mutation Spectrum and Frequency in Arabidopsis thaliana
Q57466029	Fine-tuning carbapenem resistance by reducing porin permeability of bacteria activated in the selection process of conjugation
Q50487328	Fine-tuning of chromatin composition and Polycomb recruitment by two Mi2 homologues during C. elegans early embryonic development.
Q28596118	First Draft Assembly and Annotation of the Genome of a California Endemic Oak Quercus lobata Née (Fagaceae)
Q92890450	First Estimation of the Spontaneous Mutation Rate in Diatoms
Q64242226	First Record Mutations in the Genes and Causing Leukodystrophy in Jordan
Q35825104	First complete mitochondrial genome of the South American annual fish Austrolebias charrua (Cyprinodontiformes: Rivulidae): peculiar features among cyprinodontiforms mitogenomes.
Q91893068	First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations
Q34042235	Fish the ChIPs: a pipeline for automated genomic annotation of ChIP-Seq data.
Q58616281	Fitness and Genomic Consequences of Chronic Exposure to Low Levels of Copper and Nickel in Mutation Accumulation Lines
Q35319061	Flexible and accessible workflows for improved proteogenomic analysis using the Galaxy framework
Q48165291	Flexible guide-RNA design for CRISPR applications using Protospacer Workbench.
Q46271214	Flowering Time Gene Variation in Brassica Species Shows Evolutionary Principles
Q88968433	Fludarabine and rituximab with escalating doses of lenalidomide followed by lenalidomide/rituximab maintenance in previously untreated chronic lymphocytic leukaemia (CLL): the REVLIRIT CLL-5 AGMT phase I/II study
Q95272303	FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
Q34321600	Fluorescence-based phenotypic selection allows forward genetic screens in haploid human cells
Q37622836	Forensic SNP Genotyping using Nanopore MinION Sequencing.
Q57215134	Forensic ancestry analysis in two Chinese minority populations using massively parallel sequencing of 165 ancestry-informative SNPs
Q44326729	Formation of a functional maize centromere after loss of centromeric sequences and gain of ectopic sequences
Q36166661	Found and Lost: The Fates of Horizontally Acquired Genes in Arthropod-Symbiotic Spiroplasma
Q96291703	FoxO suppresses endoplasmic reticulum stress to inhibit growth of Tsc1-deficient tissues under nutrient restriction
Q45978548	Foxh1 Occupies cis-Regulatory Modules Prior to Dynamic Transcription Factor Interactions Controlling the Mesendoderm Gene Program.
Q47914208	Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments.
Q36814625	Foxp3+ T-regulatory cells require DNA methyltransferase 1 expression to prevent development of lethal autoimmunity.
Q56459662	Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets
Q83226916	Free circular introns with an unusual branchpoint in neuronal projections
Q59691133	Frequency and signature of somatic variants in 1461 human brain exomes
Q38262833	Frequent DPH3 promoter mutations in skin cancers
Q30252418	Frequent IDH2 R172 mutations in undifferentiated and poorly-differentiated sinonasal carcinomas.
Q104515610	Frequent asymptomatic infection with tobacco ringspot virus on melon fruit
Q64117427	Frequent germline mutations of in sporadic subcutaneous panniculitis-like T-cell lymphoma
Q38855694	Frequent methylation of the KLOTHO gene and overexpression of the FGFR4 receptor in invasive ductal carcinoma of the breast.
Q90828086	Frequent mutations of genes encoding vacuolar H+ -ATPase components in granular cell tumors
Q35907666	Frequent variations in cancer-related genes may play prognostic role in treatment of patients with chronic myeloid leukemia.
Q36619566	From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula
Q89759731	From astrocytoma to glioblastoma: a clonal evolution study
Q38763141	From genetic associations to functional studies in multiple sclerosis.
Q31137675	From next-generation resequencing reads to a high-quality variant data set.
Q36668920	From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software
Q50226177	Fruit carotenoid-deficient mutants in tomato reveal a function of the plastidial isopentenyl diphosphate isomerase (IDI1) in carotenoid biosynthesis.
Q52589942	Full Genome Sequencing Reveals New Southern African Territories Genotypes Bringing Us Closer to Understanding True Variability of Foot-and-Mouth Disease Virus in Africa.
Q36148562	Full-Length Isoform Sequencing Reveals Novel Transcripts and Substantial Transcriptional Overlaps in a Herpesvirus
Q36255382	Full-length single-cell RNA-seq applied to a viral human cancer: applications to HPV expression and splicing analysis in HeLa S3 cells
Q35018130	Function and evolution of DNA methylation in Nasonia vitripennis
Q89831508	Functional Heterogeneity within the Developing Zebrafish Epicardium
Q98224394	Functional Validation of CLDN Variants Identified in a Neural Tube Defect Cohort Demonstrates Their Contribution to Neural Tube Defects
Q35551730	Functional analysis of the microtubule-interacting transcriptome
Q33741094	Functional anatomy of the immunoglobulin heavy chain 3΄ super-enhancer needs not only core enhancer elements but also their unique DNA context
Q35590286	Functional and mechanistic studies of XPC DNA-repair complex as transcriptional coactivator in embryonic stem cells
Q90421910	Functional confirmation that the R1488* variant in SCN9A results in complete loss-of-function of Nav1.7.
Q33701265	Functional dissection of NEAT1 using genome editing reveals substantial localization of the NEAT1_1 isoform outside paraspeckles
Q39688289	Functional interdependence of BRD4 and DOT1L in MLL leukemia
Q100427932	Functional role of Tet-mediated RNA hydroxymethylcytosine in mouse ES cells and during differentiation
Q37701282	Functional signature for the recognition of specific target mRNAs by human Staufen1 protein.
Q36180589	Functional variants of human papillomavirus type 16 demonstrate host genome integration and transcriptional alterations corresponding to their unique cancer epidemiology.
Q92153986	Functionally Annotating Regulatory Elements in the Equine Genome Using Histone Mark ChIP-Seq
Q103825998	Functionally impaired plasmacytoid dendritic cells and non-haematopoietic sources of type I interferon characterize human autoimmunity
Q92763644	Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency
Q64073314	Fungal acetylome comparative analysis identifies an essential role of acetylation in human fungal pathogen virulence
Q102053964	Fungal-bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds
Q38369216	Fungus Causing White-Nose Syndrome in Bats Accumulates Genetic Variability in North America with No Sign of Recombination
Q55059859	Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy.
Q33551414	G quadruplexes are genomewide targets of transcriptional helicases XPB and XPD.
Q36293353	GATA family members as inducers for cellular reprogramming to pluripotency
Q48009718	GATA4 loss of function in liver cancer impedes precursor to hepatocyte transition
Q36385889	GATA4 represses an ileal program of gene expression in the proximal small intestine by inhibiting the acetylation of histone H3, lysine 27.
Q30583255	GBSA: a comprehensive software for analysing whole genome bisulfite sequencing data.
Q91991483	GCNA Interacts with Spartan and Topoisomerase II to Regulate Genome Stability
Q30418169	GEMINI: integrative exploration of genetic variation and genome annotations
Q36185343	GENE REGULATION. Discrete functions of nuclear receptor Rev-erbα couple metabolism to the clock.
Q35448871	GINDEL: accurate genotype calling of insertions and deletions from low coverage population sequence reads
Q56397937	GIVE: portable genome browsers for personal websites
Q35537214	GNAS and KRAS Mutations Define Separate Progression Pathways in Intraductal Papillary Mucinous Neoplasm-Associated Carcinoma
Q58616990	GNE myopathy in Chinese population: hotspot and novel mutations
Q21128696	GROM-RD: resolving genomic biases to improve read depth detection of copy number variants
Q64057242	GWAS for quantitative resistance phenotypes in Mycobacterium tuberculosis reveals resistance genes and regulatory regions
Q91641973	Gauging genetic diversity of generalists: A test of genetic and ecological generalism with RNA virus experimental evolution
Q52720862	Gcn4 Binding in Coding Regions Can Activate Internal and Canonical 5' Promoters in Yeast.
Q61804723	GenESysV: a fast, intuitive and scalable genome exploration open source tool for variants generated from high-throughput sequencing projects
Q33959270	GenExp: an interactive web-based genomic DAS client with client-side data rendering
Q92538627	Gene Fusions Derived by Transcriptional Readthrough are Driven by Segmental Duplication in Human
Q36939219	Gene Mutation Profiles in Primary Diffuse Large B Cell Lymphoma of Central Nervous System: Next Generation Sequencing Analyses
Q54960366	Gene Presence-Absence Polymorphism in Castrating Anther-Smut Fungi: Recent Gene Gains and Phylogeographic Structure.
Q37369056	Gene dysregulation by histone variant H2A.Z in bladder cancer
Q38879634	Gene expression atlas of pigeonpea and its application to gain insights into genes associated with pollen fertility implicated in seed formation
Q92332172	Gene expression in blood from an individual with β-thalassemia: An RNA sequence analysis
Q38788399	Gene regulatory mechanisms underpinning prostate cancer susceptibility
Q36285449	Gene structure in the sea urchin Strongylocentrotus purpuratus based on transcriptome analysis.
Q92561700	Gene-Specific H1 Eviction through a Transcriptional Activator→p300→NAP1→H1 Pathway
Q48338509	Gene-body chromatin modification dynamics mediate epigenome differentiation in Arabidopsis.
Q36214668	Generating Multiple Base-Resolution DNA Methylomes Using Reduced Representation Bisulfite Sequencing
Q35920812	Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Q36383198	Generation of a Maize B Centromere Minimal Map Containing the Central Core Domain
Q92703125	Genes Controlled by DNA Methylation Are Involved in Wilms Tumor Progression
Q38063580	Genes, behavior and next-generation RNA sequencing.
Q87997279	Genetic Alterations in Essential Thrombocythemia Progression to Acute Myeloid Leukemia: A Case Series and Review of the Literature
Q41156085	Genetic Analyses of the NF1 Gene in Turkish Neurofibromatosis Type I Patients and Definition of three Novel Variants
Q59359110	Genetic Characterization of the Patois Serogroup (Genus ; Family ) and Evidence That Estero Real Virus is a Member of the Genus
Q46263804	Genetic Drift and Indel Mutation in the Evolution of Yeast Mitochondrial Genome Size
Q42678820	Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes
Q49828986	Genetic Separation of Listeria monocytogenes Causing Central Nervous System Infections in Animals.
Q55523920	Genetic alterations analysis in prognostic stratified groups identified TP53 and ARID1A as poor clinical performance markers in intrahepatic cholangiocarcinoma.
Q33829598	Genetic alterations in seborrheic keratoses.
Q100559752	Genetic alterations of SUGP1 mimic mutant-SF3B1 splice pattern in lung adenocarcinoma and other cancers
Q36844915	Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
Q52605253	Genetic analysis of a congenital split‑hand/split‑foot malformation 4 pedigree.
Q37572813	Genetic analysis of microglandular adenosis and acinic cell carcinomas of the breast provides evidence for the existence of a low-grade triple-negative breast neoplasia family
Q41195725	Genetic analysis of uterine adenosarcomas and phyllodes tumors of the breast
Q33693912	Genetic and clonal dissection of murine small cell lung carcinoma progression by genome sequencing
Q57454031	Genetic and epigenetic determinants establish a continuum of Hsf1 occupancy and activity across the yeast genome
Q92296632	Genetic basis of functional variability in adhesion G protein-coupled receptors
Q37301932	Genetic changes of non-small cell lung cancer under neoadjuvant therapy
Q38716624	Genetic characterization, molecular epidemiology, and phylogenetic relationships of insect-specific viruses in the taxon Negevirus
Q92830480	Genetic compensation triggered by mutant mRNA degradation
Q100307115	Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families
Q48190630	Genetic determinants and epigenetic effects of pioneer-factor occupancy.
Q36413849	Genetic determinants of FOXM1 overexpression in epithelial ovarian cancer and functional contribution to cell cycle progression
Q91447863	Genetic diversity of porcine reproductive and respiratory syndrome virus 1 in the United States of America from 2010 to 2018
Q41926643	Genetic economy in picornaviruses: Foot-and-mouth disease virus replication exploits alternative precursor cleavage pathways.
Q37578024	Genetic evidence that Nkx2.2 acts primarily downstream of Neurog3 in pancreatic endocrine lineage development
Q36502518	Genetic heterogeneity of RPMI-8402, a T-acute lymphoblastic leukemia cell line
Q36567845	Genetic heterogeneity of diffuse large B-cell lymphoma
Q40238692	Genetic hurdles limit the arms race between Prochlorococcus and the T7-like podoviruses infecting them
Q33664484	Genetic interrogation of circulating multiple myeloma cells at single-cell resolution
Q48291446	Genetic landscape of papillary thyroid carcinoma in the Chinese population.
Q52688263	Genetic mutations associated with lung cancer metastasis to the brain.
Q37085985	Genetic mutations associated with metastatic clear cell renal cell carcinoma
Q53692223	Genetic profiling of Mycobacterium bovis strains from slaughtered cattle in Eritrea.
Q101403214	Genetic profiling of Vietnamese population from large-scale genomic analysis of non-invasive prenatal testing data
Q37580860	Genetic separation of southern and northern soybean breeding programs in North America and their associated allelic variation at four maturity loci
Q36826330	Genetic signatures of Mycobacterium tuberculosis Nonthaburi genotype revealed by whole genome analysis of isolates from tuberculous meningitis patients in Thailand.
Q31110916	Genetic testing for TMEM154 mutations associated with lentivirus susceptibility in sheep
Q42532351	Genetic variant representation, annotation and prioritization in the post-GWAS era.
Q55479814	Genetic variants associated with Alzheimer's disease confer different cerebral cortex cell-type population structure.
Q64235930	Genetic variants in cardiac calcification in Northern Sweden
Q28655798	Genetic variation of the whole ICAM4 gene in Caucasians and African Americans
Q41268222	Geno viewer, a SAM/BAM viewer tool
Q36342871	Genome Analysis of Latin American Cervical Cancer: Frequent Activation of the PIK3CA Pathway
Q35801696	Genome Analysis of Pseudomonas fluorescens PCL1751: A Rhizobacterium that Controls Root Diseases and Alleviates Salt Stress for Its Plant Host
Q52326284	Genome Annotation Generator: a simple tool for generating and correcting WGS annotation tables for NCBI submission.
Q28292290	Genome Maps, a new generation genome browser
Q99602837	Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
Q36473412	Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
Q34533654	Genome Sequencing of Xanthomonas vasicola Pathovar vasculorum Reveals Variation in Plasmids and Genes Encoding Lipopolysaccharide Synthesis, Type-IV Pilus and Type-III Secretion Effectors
Q58702723	Genome Wide Identification of Mutational Hotspots in the Apicomplexan Parasite Neospora caninum and the Implications for Virulence
Q55426160	Genome data uncover four synergistic key regulators for extremely small body size in horses.
Q45071452	Genome diversity of tuber-bearing Solanum uncovers complex evolutionary history and targets of domestication in the cultivated potato
Q34200605	Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
Q50041474	Genome editing in Kluyveromyces and Ogataea yeasts using a broad-host-range Cas9/gRNA co-expression plasmid.
Q21560957	Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment
Q64987506	Genome plasticity in Candida albicans is driven by long repeat sequences.
Q42778174	Genome re-annotation of the wild strawberry Fragaria vesca using extensive Illumina- and SMRT-based RNA-seq datasets
Q37596109	Genome reference and sequence variation in the large repetitive central exon of human MUC5AC.
Q41349092	Genome sequence comparison of Aspergillus fumigatus strains isolated from patients with pulmonary aspergilloma and chronic necrotizing pulmonary aspergillosis.
Q46251945	Genome sequence of Japanese oak silk moth, Antheraea yamamai: the first draft genome in family Saturniidae
Q92450184	Genome sequence of Pseudomonas aeruginosa PAO1161, a PAO1 derivative with the ICEPae1161 integrative and conjugative element
Q34267669	Genome sequence of Shigella flexneri serotype 5a strain M90T Sm
Q35943263	Genome sequence of Vibrio sp. strain EJY3, an agarolytic marine bacterium metabolizing 3,6-anhydro-L-galactose as a sole carbon source.
Q64069453	Genome sequence of the corn leaf aphid (Rhopalosiphum maidis Fitch)
Q37518900	Genome sequencing accuracy by RCA-seq versus long PCR template cloning and sequencing in identification of human papillomavirus type 58.
Q55308953	Genome sequencing analysis of Streptomyces coelicolor mutants that overcome the phosphate-depending vancomycin lethal effect.
Q92961199	Genome sequencing in cytogenetics: Comparison of short-read and linked-read approaches for germline structural variant detection and characterization
Q57172482	Genome wide analysis of meiotic recombination in yeast: For a few SNPs more
Q34704997	Genome wide analysis of the complete GlnR nitrogen-response regulon in Mycobacterium smegmatis
Q49994322	Genome-Based Comparison of Clostridioides difficile: Average Amino Acid Identity Analysis of Core Genomes.
Q90749475	Genome-Wide Adductomics Analysis Reveals Heterogeneity in the Induction and Loss of Cyclobutane Thymine Dimers across Both the Nuclear and Mitochondrial Genomes
Q36012010	Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours.
Q30299913	Genome-Wide Analysis Uncovers Novel Recurrent Alterations in Primary Central Nervous System Lymphomas.
Q35847076	Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours
Q33362273	Genome-Wide Characterization of Maize Small RNA Loci and Their Regulation in the required to maintain repression6-1 (rmr6-1) Mutant and Long-Term Abiotic Stresses
Q42230462	Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions.
Q92072594	Genome-Wide Comparisons of Mutations Induced by Carbon-Ion Beam and Gamma-Rays Irradiation in Rice via Resequencing Multiple Mutants
Q28602947	Genome-Wide Estimates of Mutation Rates and Spectrum in Schizosaccharomyces pombe Indicate CpG Sites are Highly Mutagenic Despite the Absence of DNA Methylation
Q33735743	Genome-Wide Estimates of Transposable Element Insertion and Deletion Rates in Drosophila Melanogaster
Q97420947	Genome-Wide Identification of a Regulatory Mutation in BMP15 Controlling Prolificacy in Sheep
Q47381434	Genome-Wide Mapping of Decay Factor-mRNA Interactions in Yeast Identifies Nutrient-Responsive Transcripts as Targets of the Deadenylase Ccr4.
Q51415181	Genome-Wide Mapping of Protein-DNA Interactions on Nascent Chromatin.
Q36481528	Genome-Wide Mapping of the Binding Sites and Structural Analysis of Kaposi's Sarcoma-Associated Herpesvirus Viral Interferon Regulatory Factor 2 Reveal that It Is a DNA-Binding Transcription Factor.
Q93095338	Genome-Wide Measurement and Computational Analysis of Transcription Factor Binding and Chromatin Accessibility in Lymphocytes
Q36440362	Genome-Wide Mutational Signature of the Chemotherapeutic Agent Mitomycin C in Caenorhabditis elegans
Q109650018	Genome-Wide Profiling Reveals Alternative Polyadenylation of Innate Immune-Related mRNA in Patients With COVID-19
Q36355966	Genome-Wide Profiling of Histone Modifications and Histone Variants in Arabidopsis thaliana and Marchantia polymorpha.
Q35692482	Genome-Wide Reprogramming of Transcript Architecture by Temperature Specifies the Developmental States of the Human Pathogen Histoplasma
Q50034338	Genome-Wide STAT3 Binding Analysis after Histone Deacetylase Inhibition Reveals Novel Target Genes in Dendritic Cells.
Q37746482	Genome-Wide Screen Reveals sec21 Mutants of Saccharomyces cerevisiae Are Methotrexate-Resistant
Q38648414	Genome-Wide Sensitivity Analysis of the Microsymbiont Sinorhizobium meliloti to Symbiotically Important, Defensin-Like Host Peptides
Q37592700	Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans
Q50097481	Genome-Wide circRNA Profiling from RNA-seq Data.
Q39283161	Genome-scale analysis of the non-cultivable Treponema pallidum reveals extensive within-patient genetic variation
Q33569318	Genome-wide (over)view on the actions of vitamin D
Q34789573	Genome-wide DNA methylation analysis reveals a potential mechanism for the pathogenesis and development of uterine leiomyomas
Q59791185	Genome-wide Estrogen Receptor-α activation is sustained, not cyclical
Q36850429	Genome-wide RNAi screens in human brain tumor isolates reveal a novel viability requirement for PHF5A
Q40408213	Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
Q21266670	Genome-wide analyses of Epstein-Barr virus reveal conserved RNA structures and a novel stable intronic sequence RNA
Q34720303	Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis
Q36652760	Genome-wide analysis of KAP1, the 7SK snRNP complex, and RNA polymerase II.
Q41514063	Genome-wide analysis of alternative splicing landscapes modulated during plant-virus interactions in Brachypodium distachyon.
Q42236156	Genome-wide analysis of mutations in mutant lineages selected following fast-neutron irradiation mutagenesis of Arabidopsis thaliana
Q36180219	Genome-wide analysis of p63 binding sites identifies AP-2 factors as co-regulators of epidermal differentiation
Q51415384	Genome-wide analysis of replication timing by next-generation sequencing with E/L Repli-seq.
Q35630360	Genome-wide analysis of small nucleolar RNAs of Leishmania major reveals a rich repertoire of RNAs involved in modification and processing of rRNA.
Q52334530	Genome-wide analysis of the regulation of Cu metabolism in Cryptococcus neoformans.
Q89076066	Genome-wide analysis of the spatiotemporal regulation of firing and dormant replication origins in human cells
Q30458169	Genome-wide analysis reveals characteristics of off-target sites bound by the Cas9 endonuclease.
Q48210394	Genome-wide analysis reveals specificities of Cpf1 endonucleases in human cells
Q34313018	Genome-wide and single-cell analyses reveal a context dependent relationship between CBP recruitment and gene expression
Q40141021	Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma.
Q97418199	Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors
Q34968567	Genome-wide association of mediator and RNA polymerase II in wild-type and mediator mutant yeast
Q88968486	Genome-wide association study identifies loci associated with milk leukocyte phenotypes following experimental challenge with Streptococcus uberis
Q35889279	Genome-wide binding analysis of the transcriptional regulator TrmBL1 in Pyrococcus furiosus
Q50528544	Genome-wide binding site analysis of FAR-RED ELONGATED HYPOCOTYL3 reveals its novel function in Arabidopsis development.
Q40165187	Genome-wide characterization reveals complex interplay between TP53 and TP63 in response to genotoxic stress
Q36684836	Genome-wide coexpression of steroid receptors in the mouse brain: Identifying signaling pathways and functionally coordinated regions
Q64943540	Genome-wide comparative analysis in Solanaceous species reveals evolution of microRNAs targeting defense genes in Capsicum spp.
Q35493806	Genome-wide depletion of replication initiation events in highly transcribed regions
Q40083025	Genome-wide discovery of novel M1T1 group A streptococcal determinants important for fitness and virulence during soft-tissue infection.
Q92121422	Genome-wide discovery of the daily transcriptome, DNA regulatory elements and transcription factor occupancy in the monarch butterfly brain
Q90042573	Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni
Q47926307	Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia.
Q55129542	Genome-wide excision repair in Arabidopsis is coupled to transcription and reflects circadian gene expression patterns.
Q36266332	Genome-wide exonic small interference RNA-mediated gene silencing regulates sexual reproduction in the homothallic fungus Fusarium graminearum
Q35131055	Genome-wide features of neuroendocrine regulation in Drosophila by the basic helix-loop-helix transcription factor DIMMED.
Q46722623	Genome-wide histone acetylation correlates with active transcription in maize
Q37473013	Genome-wide identification and characterisation of human DNA replication origins by initiation site sequencing (ini-seq).
Q60048618	Genome-wide identification of RETINOBLASTOMA RELATED 1 binding sites in Arabidopsis reveals novel DNA damage regulators
Q38879390	Genome-wide identification of Wnt/β-catenin transcriptional targets during Xenopus gastrulation.
Q34831419	Genome-wide identification of binding sites for NAC and YABBY transcription factors and co-regulated genes during soybean seedling development by ChIP-Seq and RNA-Seq
Q92786450	Genome-wide identification of histone methylation (H3K9me2) and acetylation (H4K12ac) marks in two ecotypes of switchgrass (Panicum virgatum L.).
Q34332639	Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation.
Q42796095	Genome-wide mapping of DNase I hypersensitive sites in rare cell populations using single-cell DNase sequencing
Q51419224	Genome-wide mapping of endogenous G-quadruplex DNA structures by chromatin immunoprecipitation and high-throughput sequencing.
Q90526979	Genome-wide mapping of nucleotide excision repair with XR-seq
Q57285697	Genome-wide mapping reveals conserved and diverged R-loop activities in the unusual genetic landscape of the African trypanosome genome
Q86380048	Genome-wide methylation analysis in vestibular schwannomas shows putative mechanisms of gene expression modulation and global hypomethylation at the HOX gene cluster
Q34102972	Genome-wide mutant fitness profiling identifies nutritional requirements for optimal growth of Yersinia pestis in deep tissue
Q35503394	Genome-wide next-generation DNA and RNA sequencing reveals a mutation that perturbs splicing of the phosphatidylinositol glycan anchor biosynthesis class H gene (PIGH) and causes arthrogryposis in Belgian Blue cattle
Q36352703	Genome-wide patterns of latitudinal differentiation among populations of Drosophila melanogaster from North America
Q36135171	Genome-wide positioning of bivalent mononucleosomes.
Q35969015	Genome-wide profiling of RNA polymerase transcription at nucleotide resolution in human cells with native elongating transcript sequencing.
Q57035926	Genome-wide profiling of histone H3K27 acetylation featured fatty acid signalling in pancreatic beta cells in diet-induced obesity in mice
Q64970181	Genome-wide profiling of the alternative splicing provides insights into development in Plutella xylostella.
Q34592761	Genome-wide redistribution of BRD4 binding sites in transformation resistant cells
Q36306107	Genome-wide redistribution of H3K27me3 is linked to genotoxic stress and defective growth
Q36980674	Genome-wide redistribution of MeCP2 in dorsal root ganglia after peripheral nerve injury
Q37518199	Genome-wide sequencing reveals two major sub-lineages in the genetically monomorphic pathogen xanthomonas campestris pathovar musacearum
Q35162344	Genome-wide snapshot of chromatin regulators and states in Xenopus embryos by ChIP-Seq
Q57147476	Genome-wide somatic variant calling using localized colored de Bruijn graphs
Q36252998	Genome-wide standing variation facilitates long-term response to bidirectional selection for antibody response in chickens
Q33359052	Genome-wide study of KNOX regulatory network reveals brassinosteroid catabolic genes important for shoot meristem function in rice
Q37711612	Genome-wide transcription-coupled repair in Escherichia coli is mediated by the Mfd translocase
Q28253567	GenomeView: a next-generation genome browser
Q42080229	Genomes and transcriptomes of partners in plant-fungal-interactions between canola (Brassica napus) and two Leptosphaeria species
Q36746904	Genomic Analysis of Storage Protein Deficiency in Genetically Related Lines of Common Bean (Phaseolus vulgaris)
Q44874982	Genomic Analysis of the DNA Replication Timing Program during Mitotic S Phase in Maize (Zea mays) Root Tips
Q96953562	Genomic Characterization of Mycobacterium leprae to Explore Transmission Patterns Identifies New Subtype in Bangladesh
Q28603004	Genomic Characterization of Yogue, Kasokero, Issyk-Kul, Keterah, Gossas, and Thiafora Viruses: Nairoviruses Naturally Infecting Bats, Shrews, and Ticks
Q90680980	Genomic Characterization of the Periwinkle Leaf Yellowing (PLY) Phytoplasmas in Taiwan
Q34412371	Genomic DNA copy-number alterations of the let-7 family in human cancers
Q38602104	Genomic Determinants of Protein Abundance Variation in Colorectal Cancer Cells.
Q48174403	Genomic Diversity in the Endosymbiotic Bacterium Rhizobium leguminosarum.
Q98577525	Genomic Diversity of SARS-CoV-2 During Early Introduction into the United States National Capital Region
Q62746983	Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer
Q88670394	Genomic Heterogeneity and the Small Renal Mass
Q50020655	Genomic Identification and Functional Characterization of Essential Genes in Caenorhabditis elegans.
Q89510134	Genomic Landscape of Young-Onset Bladder Cancer and Its Prognostic Implications on Adult Bladder Cancer
Q104130368	Genomic RNA Elements Drive Phase Separation of the SARS-CoV-2 Nucleocapsid
Q52576108	Genomic Structural Variations Affecting Virulence During Clonal Expansion of Pseudomonas syringae pv. actinidiae Biovar 3 in Europe.
Q29010741	Genomic Support for a Moa-Tinamou Clade and Adaptive Morphological Convergence in Flightless Ratites
Q35870339	Genomic Targets and Features of BarA-UvrY (-SirA) Signal Transduction Systems
Q91136332	Genomic analysis reveals recurrent deletion of JAK-STAT signaling inhibitors HNRNPK and SOCS1 in mycosis fungoides
Q36001763	Genomic and Molecular Characterization of Miltefosine Resistance in Leishmania infantum Strains with Either Natural or Acquired Resistance through Experimental Selection of Intracellular Amastigotes
Q37163051	Genomic and Transcriptomic Associations Identify a New Insecticide Resistance Phenotype for the Selective Sweep at the Cyp6g1 Locus of Drosophila melanogaster
Q58093851	Genomic and Transcriptomic Characterization Links Cell Lines with Aggressive Head and Neck Cancers
Q56594556	Genomic and environmental determinants and their interplay underlying phenotypic plasticity
Q37269294	Genomic and epigenomic analysis of high-risk prostate cancer reveals changes in hydroxymethylation and TET1.
Q36254274	Genomic and transcriptomic comparison between Staphylococcus aureus strains associated with high and low within herd prevalence of intra-mammary infection.
Q36618604	Genomic and transcriptomic hallmarks of poorly differentiated and anaplastic thyroid cancers.
Q41593604	Genomic and transcriptomic studies of an RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine)-degrading actinobacterium
Q36256943	Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Q98286405	Genomic architecture and evolutionary antagonism drive allelic expression bias in the social supergene of red fire ants
Q57050458	Genomic assemblies of newly sequenced Trypanosoma cruzi strains reveal new genomic expansion and greater complexity
Q90235545	Genomic characterisation of Cuiaba and Charleville viruses: arboviruses (family Rhabdoviridae, genus Sripuvirus) infecting reptiles and amphibians
Q34423070	Genomic characterisation of the effector complement of the potato cyst nematode Globodera pallida
Q42777609	Genomic characterization of chromosome translocations in patients with T/myeloid mixed-phenotype acute leukemia.
Q30833823	Genomic characterization of high-count MBL cases indicates that early detection of driver mutations and subclonal expansion are predictors of adverse clinical outcome
Q98471377	Genomic characterization of malignant progression in neoplastic pancreatic cysts
Q37319470	Genomic correlates of response to CTLA-4 blockade in metastatic melanoma
Q102211005	Genomic determinants for initiation and length of natural antisense transcripts in Entamoeba histolytica
Q38757999	Genomic determinants of chronic myelomonocytic leukemia
Q35224770	Genomic distribution of H3K9me2 and DNA methylation in a maize genome
Q57539937	Genomic distribution of maize facultative heterochromatin marked by trimethylation of H3K27
Q31136664	Genomic divergence between the migratory and stationary ecotypes of Atlantic cod.
Q55285916	Genomic diversity in ochratoxigenic and non ochratoxigenic strains of Aspergillus carbonarius.
Q34262322	Genomic diversity of Epstein-Barr virus genomes isolated from primary nasopharyngeal carcinoma biopsy samples.
Q51782883	Genomic diversity of Taylorella equigenitalis introduced into the United States from 1978 to 2012.
Q89555508	Genomic footprints of activated telomere maintenance mechanisms in cancer
Q59803634	Genomic insights into virulence mechanisms of Leishmania donovani: evidence from an atypical strain
Q101476027	Genomic landscape and clonal architecture of mouse oral squamous cell carcinomas dictate tumour ecology
Q59790485	Genomic landscape of oxidative DNA damage and repair reveals regioselective protection from mutagenesis
Q43690913	Genomic landscape of transcriptional and epigenetic dysregulation in early onset polyglutamine disease.
Q30419110	Genomic mapping of phosphorothioates reveals partial modification of short consensus sequences
Q57567361	Genomic profile of pseudomyxoma peritonei analyzed using next-generation sequencing and immunohistochemistry
Q92795244	Genomic profiling of primary histiocytic sarcoma reveals two molecular subgroups
Q30360213	Genomic profiling reveals mutational landscape in parathyroid carcinomas
Q37252070	Genomic resources for wild populations of the house mouse, Mus musculus and its close relative Mus spretus
Q27320583	Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.
Q47173122	Genomic signatures of 60 years of bidirectional selection for 8-week body weight in chickens
Q37197807	Genomic targets, and histone acetylation and gene expression profiling of neural HDAC inhibition
Q57174398	Genomics and Epigenetics of Malignant Mesothelioma
Q36154689	Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options
Q38174765	Genomics of alternative splicing: evolution, development and pathophysiology
Q31154892	Genomics pipelines and data integration: challenges and opportunities in the research setting.
Q90100979	Genotyping of circulating tumor DNA in cholangiocarcinoma reveals diagnostic and prognostic information
Q46368395	Geographically structured genetic variation in the Medicago lupulina-Ensifer mutualism.
Q47267611	Germ-line and somatic EPHA2 coding variants in lens aging and cataract.
Q52626311	Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori
Q52717677	Germline Genetic IKZF1 Variation and Predisposition to Childhood Acute Lymphoblastic Leukemia.
Q28115011	Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer
Q36276527	Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer
Q60912587	Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary study
Q51441565	Germline TP53 mutations result into a constitutive defect of p53 DNA binding and transcriptional response to DNA damage.
Q47109102	Germline TTN variants are enriched in PTEN-wildtype Bannayan-Riley-Ruvalcaba syndrome.
Q52584783	Germline Tissues for Optimal Somatic Variant Detection in Myelodysplastic Syndromes (MDS).
Q35834127	Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalities
Q37289800	Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors
Q39012911	Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type
Q42271393	Germline and somatic genetic changes in multicentric tumors obtained from a patient with multiple endocrine neoplasia type 1.
Q64389365	Germline cancer susceptibility gene variants, somatic second hits, and survival outcomes in patients with resected pancreatic cancer
Q37701988	Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinoma
Q42373531	Germline mutation within COL2A1 associated with lethal chondrodysplasia in a polled Holstein family
Q40053289	Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene
Q94481864	Germline whole exome sequencing of a family with appendiceal mucinous tumours presenting with pseudomyxoma peritonei
Q35014623	Giardia lamblia transcriptome analysis using TSS-Seq and RNA-Seq
Q90680944	Global Analysis of Cell Wall Genes Revealed Putative Virulence Factors in the Dermatophyte Trichophyton rubrum
Q36210023	Global Deletion of TSPO Does Not Affect the Viability and Gene Expression Profile
Q38956956	Global MEF2 target gene analysis in cardiac and skeletal muscle reveals novel regulation of DUSP6 by p38MAPK-MEF2 signaling
Q35741569	Global SUMOylation on active chromatin is an acute heat stress response restricting transcription.
Q39100509	Global alterations of DNA methylation in cholangiocarcinoma target the Wnt signaling pathway
Q28484097	Global assessment of genomic regions required for growth in Mycobacterium tuberculosis
Q37082645	Global assessment of imprinted gene expression in the bovine conceptus by next generation sequencing
Q37547195	Global bidirectional transcription of the Epstein-Barr virus genome during reactivation
Q37255788	Global cellular response to chemotherapy-induced apoptosis
Q58726423	Global characterization of the Dicer-like protein DrnB roles in miRNA biogenesis in the social amoeba Dictyostelium discoideum
Q92310051	Global distribution of white spot syndrome virus genotypes determined using a novel genotyping assay
Q62606410	Global epigenetic analysis of BDNF Val66Met mice hippocampus reveals changes in dendrite and spine remodeling genes
Q34389954	Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression
Q36068422	Global identification of hnRNP A1 binding sites for SSO-based splicing modulation.
Q42281559	Global misregulation of genes largely uncoupled to DNA methylome epimutations characterizes a congenital overgrowth syndrome.
Q41461673	Global regulation of heterochromatin spreading by Leo1.
Q90437192	Global regulation of the histone mark H3K36me2 underlies epithelial plasticity and metastatic progression
Q47096901	Global role of the bacterial post-transcriptional regulator CsrA revealed by integrated transcriptomics
Q97587521	Global translation during early development depends on the essential transcription factor PRDM10
Q64093740	Glucocorticoid Receptor-Binding and Transcriptome Signature in Cardiomyocytes
Q30660958	GobyWeb: simplified management and analysis of gene expression and DNA methylation sequencing data
Q57285035	Going the distance: optimizing RNA-Seq strategies for transcriptomic analysis of complex viral genomes
Q30838197	GrabBlur--a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files
Q36015220	Graded gene expression changes determine phenotype severity in mouse models of CRX-associated retinopathies
Q89701678	Grafting alters tomato transcriptome and enhances tolerance to an airborne virus infection
Q92918056	Gross transcriptomic analysis of Pseudomonas putida for diagnosing environmental shifts
Q37409710	H3F3A K27M mutations in thalamic gliomas from young adult patients
Q47139599	H3K14ac is linked to methylation of H3K9 by the triple Tudor domain of SETDB1.
Q64077203	H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
Q40985261	H3K4 Methylation-Dependent Memory of Somatic Cell Identity Inhibits Reprogramming and Development of Nuclear Transfer Embryos
Q59134782	H3K9 methyltransferases and demethylases control lung tumor-propagating cells and lung cancer progression
Q91892521	HBO1 is required for the maintenance of leukaemia stem cells
Q40892042	HBOC multi-gene panel testing: comparison of two sequencing centers
Q64261955	HDAC9 complex inhibition improves smooth muscle-dependent stenotic vascular disease
Q30940080	HEPeak: an HMM-based exome peak-finding package for RNA epigenome sequencing data
Q38704133	HER2 Reactivation through Acquisition of the HER2 L755S Mutation as a Mechanism of Acquired Resistance to HER2-targeted Therapy in HER2+ Breast Cancer
Q41699409	HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype
Q36520900	HIV Tat controls RNA Polymerase II and the epigenetic landscape to transcriptionally reprogram target immune cells
Q92833135	HIV-1 DNA-capture-seq is a useful tool for the comprehensive characterization of HIV-1 provirus
Q89748520	HIV-1-induced cytokines deplete homeostatic innate lymphoid cells and expand TCF7-dependent memory NK cells
Q30666001	HMCan: a method for detecting chromatin modifications in cancer samples using ChIP-seq data.
Q37151371	HNF6 and Rev-erbα integrate hepatic lipid metabolism by overlapping and distinct transcriptional mechanisms
Q27852254	HPV-related methylation signature predicts survival in oropharyngeal squamous cell carcinomas
Q40050669	HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis
Q52631103	HSV-1-induced disruption of transcription termination resembles a cellular stress response but selectively increases chromatin accessibility downstream of genes.
Q35886890	HTLV-1 bZIP Factor Impairs Anti-viral Immunity by Inducing Co-inhibitory Molecule, T Cell Immunoglobulin and ITIM Domain (TIGIT).
Q35249211	Haploinsufficiency of ETV6 and CDKN1B in patients with acute myeloid leukemia and complex karyotype
Q88049645	Haplotype distribution and association of candidate genes with salt tolerance in Indian wild rice germplasm
Q92139302	Hdac3, Setdb1, and Kap1 mark H3K9me3/H3K14ac bivalent regions in young and aged liver
Q30457826	Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness
Q92093010	Heat stress-induced transposon activation correlates with 3D chromatin organization rearrangement in Arabidopsis
Q92992850	Helitron distribution in Brassicaceae and whole Genome Helitron density as a character for distinguishing plant species
Q51418651	Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis.
Q64056394	Hepatocyte-specific loss of GPS2 in mice reduces non-alcoholic steatohepatitis via activation of PPARα
Q38371154	Herbicide targets and detoxification proteins in sugarcane: from gene assembly to structure modelling
Q37699579	Hereditary leiomyomatosis and renal cell carcinoma syndrome-associated renal cancer: recognition of the syndrome by pathologic features and the utility of detecting aberrant succination by immunohistochemistry.
Q51701362	Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene.
Q50043331	Herpes Simplex Virus 1 Dramatically Alters Loading and Positioning of RNA Polymerase II on Host Genes Early in Infection.
Q34057278	Heterochromatin controls γH2A localization in Neurospora crassa
Q41571576	Heterogeneous Tumor-Immune Microenvironments among Differentially Growing Metastases in an Ovarian Cancer Patient.
Q92709159	Heterozygous rare genetic variants in non-syndromic early-onset obesity
Q30843060	HiChIP: a high-throughput pipeline for integrative analysis of ChIP-Seq data
Q56395478	HiGlass: web-based visual exploration and analysis of genome interaction maps
Q34613877	Hierarchical molecular tagging to resolve long continuous sequences by massively parallel sequencing
Q36725434	High Quality Maize Centromere 10 Sequence Reveals Evidence of Frequent Recombination Events
Q47581915	High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Q37236234	High expression of ZNF703 independent of amplification indicates worse prognosis in patients with luminal B breast cancer
Q55452619	High expression of the p53 isoform γ is associated with reduced progression-free survival in uterine serous carcinoma.
Q92576725	High levels of PIWI-interacting RNAs are present in the small RNA landscape of prostate epithelium from vitamin D clinical trial specimens
Q52737068	High numbers of PDCD1 (PD-1)-positive T cells and B2M mutations in microsatellite-unstable colorectal cancer.
Q91838148	High prevalence of DNA damage repair gene defects and TP53 alterations in men with treatment-naïve metastatic prostate cancer -Results from a prospective pilot study using a 37 gene panel
Q57464755	High prevalence of focal and multi-focal somatic genetic variants in the human brain
Q27026983	High throughput sequencing approaches to mutation discovery in the mouse
Q35842833	High transcript abundance, RNA editing, and small RNAs in intergenic regions within the massive mitochondrial genome of the angiosperm Silene noctiflora
Q51323498	High-Resolution Genome-Wide Mapping of Nucleosome Positioning and Occupancy Level Using Paired-End Sequencing Technology.
Q62602871	High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report
Q92214564	High-efficient and precise base editing of C•G to T•A in the allotetraploid cotton (Gossypium hirsutum) genome using a modified CRISPR/Cas9 system
Q90288030	High-fat diet fuels prostate cancer progression by rewiring the metabolome and amplifying the MYC program
Q43658331	High-intensity UV laser ChIP-seq for the study of protein-DNA interactions in living cells
Q57795854	High-resolution architecture and partner genes of rearrangements in lymphoma with DLBCL morphology
Q52359182	High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing.
Q50485002	High-resolution loss of heterozygosity screening implicates PTPRJ as a potential tumor suppressor gene that affects susceptibility to Non-Hodgkin's lymphoma.
Q33784107	High-resolution quantification of hepatitis C virus genome-wide mutation load and its correlation with the outcome of peginterferon-alpha2a and ribavirin combination therapy
Q33274578	High-resolution whole-genome analysis of skull base chordomas implicates FHIT loss in chordoma pathogenesis
Q46459571	High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome
Q30381262	High-specificity detection of rare alleles with Paired-End Low Error Sequencing (PELE-Seq).
Q40084499	High-throughput RNA sequencing in B-cell lymphomas
Q34992696	High-throughput RNA sequencing-based virome analysis of 50 lymphoma cell lines from the Cancer Cell Line Encyclopedia project
Q46500344	High-throughput m6A-seq reveals RNA m6A methylation patterns in the chloroplast and mitochondria transcriptomes of Arabidopsis thaliana
Q34333656	High-throughput multiplex HLA genotyping by next-generation sequencing using multi-locus individual tagging
Q38983113	High-throughput next-generation sequencing to genotype six classical HLA loci from 96 donors in a single MiSeq run.
Q35836890	High-throughput sequencing of human plasma RNA by using thermostable group II intron reverse transcriptases.
Q41985304	High-throughput sequencing of the synaptome in major depressive disorder
Q33562187	High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis.
Q36246008	High-throughput whole genome sequencing of Porcine reproductive and respiratory syndrome virus from cell culture materials and clinical specimens using next-generation sequencing technology
Q100946039	Higher genome mutation rates of Beijing lineage of Mycobacterium tuberculosis during human infection
Q59808057	Highly Selective 5-Formyluracil Labeling and Genome-wide Mapping Using (2-Benzimidazolyl)Acetonitrile Probe
Q55002041	Highly efficient base editing in Staphylococcus aureus using an engineered CRISPR RNA-guided cytidine deaminase.
Q46638570	Highly efficient heritable plant genome engineering using Cas9 orthologues from Streptococcus thermophilus and Staphylococcus aureus
Q34896975	Highly expressed captured genes and cross-kingdom domains present in Helitrons create novel diversity in Pleurotus ostreatus and other fungi
Q47666849	Hill-Robertson Interference Reduces Genetic Diversity on a Young Plant Y-Chromosome
Q41497014	Histone 4 lysine 8 acetylation regulates proliferation and host-pathogen interaction in Plasmodium falciparum
Q64061762	Histone H3 lysine 4 methyltransferase is required for facultative heterochromatin at specific loci
Q64080015	Histone Modifications Drive Aberrant Notch3 Expression/Activity and Growth in T-ALL
Q42511004	Histone deacetylase 3 prepares brown adipose tissue for acute thermogenic challenge.
Q40951274	Histone deacetylase class-I inhibition promotes epithelial gene expression in pancreatic cancer cells in a BRD4- and MYC-dependent manner.
Q92370754	Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate
Q92387567	Histone methyltransferases regulate the transcriptional expression of ERα and the proliferation of tamoxifen-resistant breast cancer cells
Q36144279	Histone monoubiquitination by Clock-Bmal1 complex marks Per1 and Per2 genes for circadian feedback.
Q92643099	Historical contingency shapes adaptive radiation in Antarctic fishes
Q64070446	Hominoid-Specific Transposable Elements and KZFPs Facilitate Human Embryonic Genome Activation and Control Transcription in Naive Human ESCs
Q30665213	Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs.
Q35581537	Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred.
Q36585048	Homozygosity mapping and whole-genome sequencing reveals a deep intronic PROM1 mutation causing cone-rod dystrophy by pseudoexon activation
Q33763589	Hormone-dependent control of developmental timing through regulation of chromatin accessibility
Q36281868	Host Gene Expression Is Regulated by Two Types of Noncoding RNAs Transcribed from the Epstein-Barr Virus BamHI A Rightward Transcript Region
Q36661484	Hotspots for Vitamin-Steroid-Thyroid Hormone Response Elements Within Switch Regions of Immunoglobulin Heavy Chain Loci Predict a Direct Influence of Vitamins and Hormones on B Cell Class Switch Recombination.
Q34964179	How hot are drosophila hotspots? examining recombination rate variation and associations with nucleotide diversity, divergence, and maternal age in Drosophila pseudoobscura.
Q42943393	How to Isolate a Plant's Hypomethylome in One Shot.
Q36890247	Hox-C9 activates the intrinsic pathway of apoptosis and is associated with spontaneous regression in neuroblastoma
Q59333341	HoxA9 transforms murine myeloid cells by a feedback loop driving expression of key oncogenes and cell cycle control genes
Q92517722	Hoxa13 regulates expression of common Hox target genes involved in cartilage development to coordinate the expansion of the autopodal anlage
Q34089873	HrrF is the Fur-regulated small RNA in nontypeable Haemophilus influenzae
Q36435199	Human RNase L tunes gene expression by selectively destabilizing the microRNA-regulated transcriptome.
Q33865666	Human genome-wide repair map of DNA damage caused by the cigarette smoke carcinogen benzo[a]pyrene
Q37378179	Human induced pluripotent stem cell-derived cardiomyocytes recapitulate the predilection of breast cancer patients to doxorubicin-induced cardiotoxicity
Q37123374	Human papillomavirus type 58 genome variations and RNA expression in cervical lesions
Q38705984	Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations
Q52873719	Hybrid Cellular Metabolism Coordinated by Zic3 and Esrrb Synergistically Enhances Induction of Naive Pluripotency.
Q92006491	Hybridization promotes asexual reproduction in Caenorhabditis nematodes
Q41561078	Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals
Q104749796	Hypoxia-induced suppression of alternative splicing of MBD2 promotes breast cancer metastasis via activation of FZD1
Q30694646	ICO amplicon NGS data analysis: a Web tool for variant detection in common high-risk hereditary cancer genes analyzed by amplicon GS Junior next-generation sequencing
Q90452302	IDH1 Expression via the R132H Mutation-Specific Antibody in Adrenocortical Neoplasias-Prognostic Impact in Carcinomas
Q98181408	IL-15 Preconditioning Augments CAR T Cell Responses to Checkpoint Blockade for Improved Treatment of Solid Tumors
Q55517096	INSaFLU: an automated open web-based bioinformatics suite "from-reads" for influenza whole-genome-sequencing-based surveillance.
Q47110684	INTEGRATE-Vis: a tool for comprehensive gene fusion visualization
Q89991582	IRF4 instructs effector Treg differentiation and immune suppression in human cancer
Q57080588	IRF8 Regulates Transcription of Naips for NLRC4 Inflammasome Activation
Q53407519	IRS2 mutations linked to invasion in pleomorphic invasive lobular carcinoma.
Q30898093	IRcall and IRclassifier: two methods for flexible detection of intron retention events from RNA-Seq data
Q64937859	ISG20 promotes local tumor immunity and contributes to poor survival in human glioma.
Q37210954	ISL1 and JMJD3 synergistically control cardiac differentiation of embryonic stem cells
Q64231142	ISL1 predicts poor outcomes for patients with gastric cancer and drives tumor progression through binding to the ZEB1 promoter together with SETD7
Q64109194	ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy
Q39632029	Icarus: visualizer for de novo assembly evaluation
Q53126713	Identical TP53 mutations in pelvic carcinosarcomas and associated serous tubal intraepithelial carcinomas provide evidence of their clonal relationship.
Q90524318	Identification and Characterization of the First Virulent Phages, Including a Novel Jumbo Virus, Infecting Ochrobactrum spp
Q33882617	Identification and characterization of a FOXA2-regulated transcriptional enhancer at a type 2 diabetes intronic locus that controls GCKR expression in liver cells
Q61799384	Identification and characterization of a direct activator of a gene transfer agent
Q90496455	Identification and characterization of jasmonic acid- and linolenic acid-mediated transcriptional regulation of secondary laticifer differentiation in Hevea brasiliensis
Q35655079	Identification and characterization of long non-coding RNAs involved in osmotic and salt stress in Medicago truncatula using genome-wide high-throughput sequencing
Q51149039	Identification and characterization of long noncoding RNA in Paulownia tomentosa treated with methyl methane sulfonate.
Q31041859	Identification and correction of systematic error in high-throughput sequence data
Q42152221	Identification of 3' gene ends using transcriptional and genomic conservation across vertebrates
Q42775500	Identification of Brassinosteroid Target Genes by Chromatin Immunoprecipitation Followed by High-Throughput Sequencing (ChIP-seq) and RNA-Sequencing.
Q42710918	Identification of Complete Repertoire of Apis florea Odorant Receptors Reveals Complex Orthologous Relationships with Apis mellifera.
Q64108136	Identification of DNA-Methylated CpG Islands Associated With Gene Silencing in the Adult Body Tissues of the Ogye Chicken Using RNA-Seq and Reduced Representation Bisulfite Sequencing
Q49958017	Identification of G-quadruplex clusters by high-throughput sequencing of whole-genome amplified products with a G-quadruplex ligand.
Q36133597	Identification of HIV Mutation as Diagnostic Biomarker through Next Generation Sequencing
Q36060915	Identification of Highly Variable Supernumerary Chromosome Segments in an Asexual Pathogen.
Q35877841	Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study
Q47141591	Identification of MYLK3 mutations in familial dilated cardiomyopathy
Q52595198	Identification of Plasmid-Encoded sRNAs in a blaNDM-1-Harboring Multidrug-Resistance Plasmid pNDM-HK in Enterobacteriaceae.
Q35616182	Identification of Reproduction-Related Gene Polymorphisms Using Whole Transcriptome Sequencing in the Large White Pig Population
Q98195425	Identification of SNPs and InDels associated with berry size in table grapes integrating genetic and transcriptomic approaches
Q36418130	Identification of Source of Brucella suis Infection in Human by Using Whole-Genome Sequencing, United States and Tonga
Q90113804	Identification of Structural Variation in Chimpanzees Using Optical Mapping and Nanopore Sequencing
Q50063994	Identification of Two Distinct Classes of the Human INO80 Complex Genome-Wide.
Q92755189	Identification of a Master Regulator of Differentiation in Toxoplasma
Q29035744	Identification of a Novel Hepacivirus in Domestic Cattle from Germany
Q28550467	Identification of a Novel Lipoprotein Regulator of Clostridium difficile Spore Germination
Q38867763	Identification of a Novel Somatic Mutation Leading to Allele Dropout for EGFR L858R Genotyping in Non-Small Cell Lung Cancer
Q35666595	Identification of a common risk haplotype for canine idiopathic epilepsy in the ADAM23 gene
Q33622368	Identification of a novel RASD1 somatic mutation in a USP8-mutated corticotroph adenoma.
Q41462539	Identification of a novel coronavirus from guinea fowl using metagenomics
Q54356148	Identification of a novel de novo deletion in RAF1 associated with biventricular hypertrophy in Noonan syndrome.
Q38469149	Identification of a novel gene fusion (BMX-ARHGAP) in gastric cardia adenocarcinoma
Q51177048	Identification of a novel protein kinase that affects the chronological lifespan in fission yeast.
Q47144537	Identification of alcohol stress tolerance genes of Synechocystis sp. PCC 6803 using adaptive laboratory evolution.
Q37100216	Identification of an EMS-induced causal mutation in a gene required for boron-mediated root development by low-coverage genome re-sequencing in Arabidopsis.
Q38469377	Identification of an epigenetic signature of early mouse liver regeneration that is disrupted by Zn-HDAC inhibition
Q64075131	Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Q53204880	Identification of candidate genes associated with fertility restoration of cytoplasmic male-sterility in onion (Allium cepa L.) using a combination of bulked segregant analysis and RNA-seq.
Q56028089	Identification of candidate genes associated with mealiness and maturity date in peach [Prunus persica (L.) Batsch] using QTL analysis and deep sequencing
Q90480845	Identification of circulating tumor DNA using a targeted 545-gene next generation sequencing panel in patients with gastric cancer
Q34340569	Identification of direct targets and modified bases of RNA cytosine methyltransferases
Q96683490	Identification of distinct loci for de novo DNA methylation by DNMT3A and DNMT3B during mammalian development
Q33558039	Identification of endoribonuclease specific cleavage positions reveals novel targets of RNase III in Streptococcus pyogenes
Q50467373	Identification of genes required by Bacillus thuringiensis for survival in soil by transposon-directed insertion site sequencing.
Q50479844	Identification of genes required for soil survival in Burkholderia thailandensis by transposon-directed insertion site sequencing.
Q42024522	Identification of genomic binding sites for Candida glabrata Pdr1 transcription factor in wild-type and ρ0 cells.
Q31105081	Identification of interleukin genes in Pogona vitticeps using a de novo transcriptome assembly from RNA-seq data
Q61796834	Identification of lenalidomide resistance pathways in myeloma and targeted resensitization using cereblon replacement, inhibition of STAT3 or targeting of IRF4
Q92965003	Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosis
Q35089615	Identification of mutations in zebrafish using next-generation sequencing
Q98952074	Identification of mycobacteriophage toxic genes reveals new features of mycobacterial physiology and morphology
Q41657185	Identification of new branch points and unconventional introns in Saccharomyces cerevisiae
Q92591575	Identification of new hypoxia-regulated epithelial-mesenchymal transition marker genes labeled by H3K4 acetylation
Q35689684	Identification of new viral genes and transcript isoforms during Epstein-Barr virus reactivation using RNA-Seq
Q37401110	Identification of non-coding genetic variants in samples from hypoxemic respiratory disease patients that affect the transcriptional response to hypoxia.
Q93216612	Identification of novel HNF1B mRNA splicing variants and their qualitative and semi-quantitative profile in selected healthy and tumour tissues
Q92123999	Identification of novel genes involved in phosphate accumulation in Lotus japonicus through Genome Wide Association mapping of root system architecture and anion content
Q40722148	Identification of novel human papillomavirus lineages and sublineages in HIV/HPV-coinfected pregnant women by next-generation sequencing
Q36903712	Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system
Q92096782	Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease
Q30749239	Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases
Q34457014	Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq
Q39010754	Identification of novel transcription factors in osteoclast differentiation using genome-wide analysis of open chromatin determined by DNase-seq
Q35041982	Identification of novel transcripts and noncoding RNAs in bovine skin by deep next generation sequencing
Q48731403	Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
Q46242568	Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
Q35638426	Identification of quantitative trait loci underlying resistance to southern root-knot and reniform nematodes in soybean accession PI 567516C
Q55259551	Identification of rare de novo epigenetic variations in congenital disorders.
Q39516571	Identification of small RNAs in Mycobacterium smegmatis using heterologous Hfq
Q34573775	Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia
Q54960094	Identification of somatic mutations in monozygotic twins discordant for psychiatric disorders.
Q33836160	Identification of structural variation in mouse genomes
Q94585971	Identification of the distribution of human endogenous retroviruses K (HML-2) by PCR-based target enrichment sequencing
Q27334215	Identification of the genomic insertion site of Pmel-1 TCR α and β transgenes by next-generation sequencing
Q42665464	Identifying ChIP-seq enrichment using MACS.
Q64883926	Identifying Transcription Factor Olig2 Genomic Binding Sites in Acutely Purified PDGFRα+ Cells by Low-cell Chromatin Immunoprecipitation Sequencing Analysis.
Q57232273	Identifying molecular markers suitable for Frl selection in tomato breeding
Q34261618	Identity by descent mapping of founder mutations in cancer using high-resolution tumor SNP data
Q47114619	Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing
Q92615204	Immune signature drives leukemia escape and relapse after hematopoietic cell transplantation
Q58223804	Immune stimuli shape the small non-coding transcriptome of extracellular vesicles released by dendritic cells
Q92203199	ImmuneRegulation: a web-based tool for identifying human immune regulatory elements
Q92797185	Immunoevolution of mouse pancreatic organoid isografts from preinvasive to metastatic disease
Q90319072	Immunohistochemical detection of ALK protein identifies APC mutated medulloblastoma and differentiates the WNT-activated medulloblastoma from other types of posterior fossa childhood tumors
Q39030334	Immunomics of the koala (Phascolarctos cinereus).
Q37718264	Impact of genomic polymorphisms on the repertoire of human MHC class I-associated peptides
Q36660160	Impact of genomic structural variation in Drosophila melanogaster based on population-scale sequencing
Q30663457	Impact of library preparation on downstream analysis and interpretation of RNA-Seq data: comparison between Illumina PolyA and NuGEN Ovation protocol
Q55387060	Impact of lower uterine segment involvement in type II endometrial cancer and the unique mutational profile of serous tumors.
Q47151248	Impact of the G84E variant on HOXB13 gene and protein expression in formalin-fixed, paraffin-embedded prostate tumours.
Q61445370	Impaired LXRα Phosphorylation Attenuates Progression of Fatty Liver Disease
Q35178920	Implementation of Cloud based next generation sequencing data analysis in a clinical laboratory.
Q55449354	Implementing precision cancer medicine in the public health services of Norway: the diagnostic infrastructure and a cost estimate.
Q38902848	Implications of evolutionary engineering for growth and recombinant protein production in methanol-based growth media in the yeast Pichia pastoris.
Q92859183	Improved Genome Assembly and Annotation of the Soybean Aphid (Aphis glycines Matsumura)
Q112709246	Improved gRNA secondary structures allow editing of target sites resistant to CRISPR-Cas9 cleavage
Q34456468	Improved pipeline for reducing erroneous identification by 16S rRNA sequences using the Illumina MiSeq platform
Q59128965	Improved reference genome for the domestic horse increases assembly contiguity and composition
Q34194405	Improved structural annotation of protein-coding genes in the Meloidogyne hapla genome using RNA-Seq
Q35863944	Improving RNA-Seq Precision with MapAl
Q34430087	Improving indel detection specificity of the Ion Torrent PGM benchtop sequencer
Q34389977	Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Q34568742	Improving mutation screening in familial hematuric nephropathies through next generation sequencing
Q33637526	Improving transcriptome construction in non-model organisms: integrating manual and automated gene definition in Emiliania huxleyi
Q36132221	In Vivo Transcriptional Activation Using CRISPR/Cas9 in Drosophila
Q34037810	In depth annotation of the Anopheles gambiae mosquito midgut transcriptome.
Q34413907	In depth comparison of an individual's DNA and its lymphoblastoid cell line using whole genome sequencing
Q50204802	In silico analysis of the sequence features responsible for alternatively spliced introns in the model green alga Chlamydomonas reinhardtii.
Q48355079	In vitro expansion of mouse primordial germ cell-like cells recapitulates an epigenetic blank slate.
Q38968027	In vivo murine model of acquired resistance in myeloma reveals differential mechanisms for lenalidomide and pomalidomide in combination with dexamethasone.
Q64900178	In vivo nuclear capture and molecular profiling identifies Gmeb1 as a transcriptional regulator essential for dopamine neuron function.
Q64077633	In vivo recombination of Saccharomyces eubayanus maltose-transporter genes yields a chimeric transporter that enables maltotriose fermentation
Q55252335	In vivo reprogramming drives Kras-induced cancer development.
Q107077787	In vivo structural characterization of the SARS-CoV-2 RNA genome identifies host proteins vulnerable to repurposed drugs
Q33742547	In-depth genome characterization of a Brazilian common bean core collection using DArTseq high-density SNP genotyping.
Q36365675	In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome
Q39829557	InPhaDel: integrative shotgun and proximity-ligation sequencing to phase deletions with single nucleotide polymorphisms
Q30536439	InSilico DB genomic datasets hub: an efficient starting point for analyzing genome-wide studies in GenePattern, Integrative Genomics Viewer, and R/Bioconductor
Q41945245	Inactivation of Lsd1 triggers senescence in trophoblast stem cells by induction of Sirt4.
Q43074457	Inactivation of a GAL4-like transcription factor improves cell fitness and product yield in glycoengineered Pichia pastoris strains
Q38260979	Incorporating computational resources in a cancer research program
Q98159014	Increased frequency of ESR1 mutation in metastatic breast cancer by dosing selective estrogen receptor modulator followed by aromatase inhibitor
Q90439802	Increased frequency of germline BRCA2 mutations associates with prostate cancer metastasis in a racially diverse patient population
Q34468164	Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
Q31142768	Indel variant analysis of short-read sequencing data with Scalpel.
Q52372669	Individual retrotransposon integrants are differentially controlled by KZFP/KAP1-dependent histone methylation, DNA methylation and TET-mediated hydroxymethylation in naïve embryonic stem cells.
Q42678871	Individualized drug screening based on next generation sequencing and patient derived xenograft model for pancreatic cancer with bone metastasis
Q90838638	Individualized recovery of gut microbial strains post antibiotics
Q40973371	Indole Glucosinolate Biosynthesis Limits Phenylpropanoid Accumulation in Arabidopsis thaliana.
Q52687455	Induction and recovery of copy number variation in banana through gamma irradiation and low-coverage whole-genome sequencing.
Q47594220	Induction of H3K9me3 and DNA methylation by tethered heterochromatin factors in Neurospora crassa
Q57289394	Induction of antibacterial proteins and peptides in the coprophilous mushroom Coprinopsis cinerea in response to bacteria
Q36736766	Infection by Herpes Simplex Virus 1 Causes Near-Complete Loss of RNA Polymerase II Occupancy on the Host Cell Genome
Q21145293	Inferring clonal composition from multiple sections of a breast cancer
Q48120468	Inferring genetic origins and phenotypic traits of George Bähr, the architect of the Dresden Frauenkirche
Q37119308	Infiltrating epitheliosis of the breast: characterization of histological features, immunophenotype and genomic profile
Q92539305	Inflorescence Meristem Fate Is Dependent on Seed Development and FRUITFULL in Arabidopsis thaliana
Q64115872	Influence of p53 Isoform Expression on Survival in High-Grade Serous Ovarian Cancers
Q54210115	Influenza Virus Mounts a Two-Pronged Attack on Host RNA Polymerase II Transcription.
Q47290509	Informatics for cancer immunotherapy
Q52686318	Inherited DNA-Repair Defects in Colorectal Cancer.
Q89514576	Inhibition of IRF4 in dendritic cells by PRR-independent and -dependent signals inhibit Th2 and promote Th17 responses
Q61445491	Inhibition of monocyte-like cell extravasation protects from neurodegeneration in DBA/2J glaucoma
Q35261803	Inhibition of mutant EGFR in lung cancer cells triggers SOX2-FOXO6-dependent survival pathways
Q94591952	Injured adult neurons regress to an embryonic transcriptional growth state
Q50421956	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus.
Q35140495	Insect-specific viruses detected in laboratory mosquito colonies and their potential implications for experiments evaluating arbovirus vector competence
Q93072545	Insertion Pool Sequencing for Insertional Mutant Analysis in Complex Host-Microbe Interactions
Q90629047	Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
Q33877266	Insight into the Recent Genome Duplication of the Halophilic Yeast Hortaea werneckii: Combining an Improved Genome with Gene Expression and Chromatin Structure
Q58781272	Insights Into Mutation Variation in Lithuanian Exome
Q64087601	Insights Into the Evolution of Daptomycin Resistance From an Bioreactor Model
Q64101616	Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA Sequencing
Q21144876	Insights into the Dekkera bruxellensis genomic landscape: comparative genomics reveals variations in ploidy and nutrient utilisation potential amongst wine isolates
Q57027318	Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy
Q34485099	Insulator function and topological domain border strength scale with architectural protein occupancy
Q88707296	Integral bHLH factor regulation of cell cycle exit and RGC differentiation
Q92087496	Integrated Epigenome, Exome, and Transcriptome Analyses Reveal Molecular Subtypes and Homeotic Transformation in Uterine Fibroids
Q89597706	Integrated Genome-Wide Analysis of an Isogenic Pair of Pseudomonas aeruginosa Clinical Isolates with Differential Antimicrobial Resistance to Ceftolozane/Tazobactam, Ceftazidime/Avibactam, and Piperacillin/Tazobactam
Q55403103	Integrated Multi-Omic Analysis of Mycobacterium tuberculosis H37Ra Redefines Virulence Attributes.
Q33983489	Integrated RNA and DNA sequencing improves mutation detection in low purity tumors.
Q41133916	Integrated analysis of long non-coding RNAs in human colorectal cancer
Q37284612	Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma
Q41924355	Integrated analysis of the molecular action of Vorinostat identifies epi-sensitised targets for combination therapy.
Q34744054	Integrated analysis of whole genome and transcriptome sequencing reveals diverse transcriptomic aberrations driven by somatic genomic changes in liver cancers
Q35920853	Integrated genomic analysis suggests MLL3 is a novel candidate susceptibility gene for familial nasopharyngeal carcinoma
Q48315182	Integrated genomic characterization of adrenocortical carcinoma
Q36584991	Integrated genomic profiling identifies microRNA-92a regulation of IQGAP2 in locally advanced rectal cancer
Q38000683	Integrated inference and analysis of regulatory networks from multi-level measurements
Q91750411	Integrating Bacterial ChIP-seq and RNA-seq Data With SnakeChunks
Q28077579	Integrating Epigenomics into the Understanding of Biomedical Insight
Q36407813	Integration of Genome-Wide TF Binding and Gene Expression Data to Characterize Gene Regulatory Networks in Plant Development
Q89863505	Integration, abundance, and transmission of mutations and transgenes in a series of CRISPR/Cas9 soybean lines
Q28264933	Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
Q93115049	Integrative Molecular Characterization of Resistance to Neoadjuvant Chemoradiation in Rectal Cancer
Q95841097	Integrative Omics Analysis Reveals a Limited Transcriptional Shock After Yeast Interspecies Hybridization
Q33754852	Integrative analyses of gene expression and DNA methylation profiles in breast cancer cell line models of tamoxifen-resistance indicate a potential role of cells with stem-like properties
Q42089762	Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse.
Q28288215	Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal
Q30652671	Integrative analysis of deep sequencing data identifies estrogen receptor early response genes and links ATAD3B to poor survival in breast cancer
Q60312683	Integrative approach using Yersinia pestis genomes to revisit the historical landscape of plague during the Medieval Period
Q27853170	Integrative clinical genomics of advanced prostate cancer
Q38633199	Integrative genomic analysis by interoperation of bioinformatics tools in GenomeSpace
Q35839013	Integrative phenotyping framework (iPF): integrative clustering of multiple omics data identifies novel lung disease subphenotypes
Q60045126	Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP
Q48186198	Inter-Laboratory Evaluation of a Next-Generation Sequencing Panel for Acute Myeloid Leukemia
Q46256901	Inter-individual gene variants associated with trabecular bone plasticity: A step forward in the personal genomics of degenerative bone disease
Q48317457	Interactive visualization and analysis of large-scale sequencing datasets using ZENBU.
Q91884187	Interferon signature in patients with STAT1 gain-of-function mutation is epigenetically determined
Q63369779	Interleukin 10 mutant zebrafish have an enhanced interferon gamma response and improved survival against a Mycobacterium marinum infection
Q58716718	Internal RNAs overlapping coding sequences can drive the production of alternative proteins in archaea
Q92875181	Interplay between small RNA pathways shapes chromatin landscapes in C. elegans
Q96023037	Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma
Q42773657	Interpretation, stratification and evidence for sequence variants affecting mRNA splicing in complete human genome sequences
Q93106472	Interrogating Mutant Allele Expression via Customized Reference Genomes to Define Influential Cancer Mutations
Q64289907	Interspecies conservation of organisation and function between nonhomologous regional centromeres
Q35530031	Interspecific and intraspecific gene variability in a 1-Mb region containing the highest density of NBS-LRR genes found in the melon genome
Q36559698	Intestinal master transcription factor CDX2 controls chromatin access for partner transcription factor binding
Q36410147	Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy
Q91887235	Intra-individual variation of circulating tumour DNA in lung cancer patients
Q59064996	Intra-tumour diversification in colorectal cancer at the single-cell level
Q33587363	Intracellular lipid binding protein family diversity from Oyster Crassostrea gigas: genomic and structural features of invertebrate lipid transporters
Q30443828	Intracytoplasmic copper homeostasis controls cytochrome c oxidase production
Q38953705	Intragenic anaplastic lymphoma kinase (ALK) rearrangements: translocations as a novel mechanism of ALK activation in neuroblastoma tumors.
Q34339024	Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1.
Q41520220	Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer
Q39229528	Intron retention as a component of regulated gene expression programs.
Q104459103	Intron retention is a robust marker of intertumoral heterogeneity in pancreatic ductal adenocarcinoma
Q64990890	Intron retention is a source of neoepitopes in cancer.
Q37741521	Intronic polyadenylation of PDGFRα in resident stem cells attenuates muscle fibrosis.
Q48182949	Investigating Potential Chromosomal Rearrangements during Laboratory Culture of Neisseria gonorrhoeae
Q92330185	Investigating the role of super-enhancer RNAs underlying embryonic stem cell differentiation
Q42760068	Investigation of Somatic GNAQ, GNA11, BAP1 and SF3B1 Mutations in Ophthalmic Melanocytomas
Q40800645	Investigation of Viral and Host Chromatin by ChIP-PCR or ChIP-Seq Analysis
Q36335892	Investigation of mutations in the HBB gene using the 1,000 genomes database
Q37260761	Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples
Q57092242	Investigation of the Plasma Virome from Cases of Unexplained Febrile Illness in Tanzania from 2013 to 2014: a Comparative Analysis between Unbiased and VirCapSeq-VERT High-Throughput Sequencing Approaches
Q36657199	Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle.
Q92831987	Involvement of a G Protein Regulatory Circuit in Alternative Oxidase Production in Neurospora crassa
Q37556326	Ischemic Preconditioning Confers Epigenetic Repression of Mtor and Induction of Autophagy Through G9a-Dependent H3K9 Dimethylation
Q50010956	Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark.
Q88975963	Isolation and characterization of SARS-CoV-2 from the first US COVID-19 patient
Q47812031	Isolation and characterization of circulating tumor cells using a novel workflow combining the CellSearch® system and the CellCelector™.
Q64090555	Isolation, characterization and analysis of bacteriophages from the haloalkaline lake Elmenteita, Kenya
Q90348540	Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course
Q35546060	Itaya virus, a Novel Orthobunyavirus Associated with Human Febrile Illness, Peru
Q36974344	JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma
Q36793546	JBrowse: a dynamic web platform for genome visualization and analysis
Q37644459	Jmjd2c facilitates the assembly of essential enhancer-protein complexes at the onset of embryonic stem cell differentiation
Q33361956	Job Sharing in the Endomembrane System: Vacuolar Acidification Requires the Combined Activity of V-ATPase and V-PPase.
Q34756290	Joint genotype inference with germline and somatic mutations
Q39550920	Juicebox Provides a Visualization System for Hi-C Contact Maps with Unlimited Zoom
Q27317357	KDM2B is implicated in bovine lethal multi-organic developmental dysplasia
Q58798780	KDM5 histone demethylases repress immune response via suppression of STING
Q37603840	KDM5 lysine demethylases are involved in maintenance of 3'UTR length.
Q42688550	KLF4 is downregulated but not mutated during human esophageal squamous cell carcinogenesis and has tumor stage-specific functions
Q88294430	KLRG1+ Effector CD8+ T Cells Lose KLRG1, Differentiate into All Memory T Cell Lineages, and Convey Enhanced Protective Immunity
Q33744019	Kaposi's sarcoma-associated herpesvirus-encoded LANA interacts with host KAP1 to facilitate establishment of viral latency
Q28553630	KdmB, a Jumonji Histone H3 Demethylase, Regulates Genome-Wide H3K4 Trimethylation and Is Required for Normal Induction of Secondary Metabolism in Aspergillus nidulans
Q38744688	Killer Immunoglobulin-Like Receptor Allele Determination Using Next-Generation Sequencing Technology
Q98771620	Killing Two Birds With One Stone - Strain Engineering Facilitates the Development of a Unique Rhamnolipid Production Process
Q90391244	Kin28 depletionincreases association of TFIID subunits Taf1 and Taf4 with promoters in Saccharomyces cerevisiae
Q46244893	Kiwifruit SVP2 controls developmental and drought-stress pathways
Q34044769	Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME.
Q89794499	Knock down of GmVQ58 encoding a VQ motif-containing protein enhances soybean resistance to the common cutworm (Spodoptera litura Fabricius)
Q24303485	Kras(G12D) and Nkx2-1 haploinsufficiency induce mucinous adenocarcinoma of the lung
Q41845530	Krüppel-like Transcription Factor KLF10 Suppresses TGFβ-Induced Epithelial-to-Mesenchymal Transition via a Negative Feedback Mechanism
Q91806159	L3MBTL1 regulates ALS/FTD-associated proteotoxicity and quality control
Q90016756	LATS kinase-mediated CTCF phosphorylation and selective loss of genomic binding
Q37544999	LIM domain-binding 1 maintains the terminally differentiated state of pancreatic β cells.
Q91062866	LSD1-mediated repression of GFI1 super-enhancer plays an essential role in erythroleukemia
Q64102053	Laboratory Evolution of a × Hybrid Under Simulated Lager-Brewing Conditions
Q37615730	Laboratory confirmed miltefosine resistant cases of visceral leishmaniasis from India
Q96765738	Laboratory culture of the California Sea Firefly Vargula tsujii (Ostracoda: Cypridinidae): Developing a model system for the evolution of marine bioluminescence
Q36019732	Lack of Genotype and Phenotype Correlation in a Rice T-DNA Tagged Line Is Likely Caused by Introgression in the Seed Source
Q36722643	Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder
Q48248056	Lamin B1 regulates somatic mutations and progression of B-cell malignancies.
Q95933674	Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
Q90125978	Large X-linked palindromes undergo arm-to-arm gene conversion across Mus lineages
Q41901006	Large inverted duplications in the human genome form via a fold-back mechanism
Q62569091	Large-Scale Structural Variation Detection in Subterranean Clover Subtypes Using Optical Mapping
Q50096559	Large-scale genomic analysis shows association between homoplastic genetic variation in Mycobacterium tuberculosis genes and meningeal or pulmonary tuberculosis.
Q34067272	Lariat intronic RNAs in the cytoplasm of Xenopus tropicalis oocytes
Q30460694	Late Danubian mitochondrial genomes shed light into the Neolithisation of Central Europe in the 5th millennium BC.
Q62723303	Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: Diagnosis and novel mutation revealed by exome sequencing
Q34449792	Late onset spinal motor neuronopathy is caused by mutation in CHCHD10.
Q92740597	Latency and interval therapy affect the evolution in metastatic colorectal cancer
Q30979204	LayerCake: a tool for the visual comparison of viral deep sequencing data
Q30279194	Leaf shape evolution has a similar genetic architecture in three edaphic specialists within the Mimulus guttatus species complex
Q26849760	Legume genomics: understanding biology through DNA and RNA sequencing
Q37695595	Lethal Consequences of Overcoming Metabolic Restrictions Imposed on a Cooperative Bacterial Population
Q34312209	Leukemia gene atlas--a public platform for integrative exploration of genome-wide molecular data
Q37655097	Leveraging biological replicates to improve analysis in ChIP-seq experiments
Q30995841	Leveraging existing data sets to generate new insights into Alzheimer's disease biology in specific patient subsets
Q113307853	Lexicon-Mono-Seq, DOM Text Based Async MSA Viewer
Q34484579	Limitations and possibilities of low cell number ChIP-seq.
Q36560114	Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America
Q37718170	Limiting Thymic Precursor Supply Increases the Risk of Lymphoid Malignancy in Murine X-Linked Severe Combined Immunodeficiency
Q50041523	Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation.
Q37387069	Linear ubiquitination by LUBEL has a role in Drosophila heat stress response.
Q91767504	LinkedSV for detection of mosaic structural variants from linked-read exome and genome sequencing data
Q36548792	Liver-derived ketone bodies are necessary for food anticipation
Q89136368	Liver-specific knockout of histone methyltransferase G9a impairs liver maturation and dysregulates inflammatory, cytoprotective, and drug-processing genes
Q41819380	Lkb1 inactivation drives lung cancer lineage switching governed by Polycomb Repressive Complex 2.
Q33648454	LncRNAs are altered in lung squamous cell carcinoma and lung adenocarcinoma
Q64389029	Local Inversion Heterozygosity Alters Recombination throughout the Genome
Q41952216	Local potentiation of stress-responsive genes by upstream noncoding transcription
Q38733840	Local regulation of gene expression by lncRNA promoters, transcription and splicing.
Q90370352	Localized calcium signaling and the control of coupling at Cx36 gap junctions
Q89495295	Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform
Q43924342	Loci associated with skin pigmentation identified in African populations.
Q37679760	Locus- and cell type-specific epigenetic switching during cellular differentiation in mammals
Q36577607	Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells.
Q34885158	Long Non-Coding RNA BST2/BISPR is Induced by IFN and Regulates the Expression of the Antiviral Factor Tetherin.
Q88558433	Long Noncoding RNAs AC009014.3 and Newly Discovered XPLAID Differentiate Aggressive and Indolent Prostate Cancers
Q57635195	Long genes linked to autism spectrum disorders harbor broad enhancer-like chromatin domains
Q33687024	Long non-coding RNA PARTICLE bridges histone and DNA methylation
Q35538795	Long non-coding RNA discovery across the genus anopheles reveals conserved secondary structures within and beyond the Gambiae complex
Q58101203	Long non-coding RNAs have age-dependent diurnal expression that coincides with age-related changes in genome-wide facultative heterochromatin
Q36446804	Long non-coding RNAs in innate and adaptive immunity
Q38625682	Long noncoding RNAs in T lymphocytes
Q45939332	Long-Read Sequencing of Human Cytomegalovirus Transcriptome Reveals RNA Isoforms Carrying Distinct Coding Potentials.
Q41868468	Long-range PCR in next-generation sequencing: comparison of six enzymes and evaluation on the MiSeq sequencer
Q57454043	Long-read sequence capture of the hemoglobin gene clusters across gadid species
Q88562679	Long-read sequencing data analysis for yeasts
Q47150153	Long-read sequencing of the human cytomegalovirus transcriptome with the Pacific Biosciences RSII platform.
Q64053851	Long-read sequencing reveals a 4.4 kb tandem repeat region in the mitogenome of Echinococcus granulosus (sensu stricto) genotype G1
Q93052882	Long-read sequencing unveils IGH-DUX4 translocation into the silenced IGH allele in B-cell acute lymphoblastic leukemia
Q103805205	Long-read trio sequencing of individuals with unsolved intellectual disability
Q38870624	Long-term Benefit of PD-L1 Blockade in Lung Cancer Associated with JAK3 Activation
Q99586011	Long-term expansion with germline potential of human primordial germ cell-like cells in vitro
Q36132307	Longevity Genes Revealed by Integrative Analysis of Isoform-Specific daf-16/FoxO Mutants of Caenorhabditis elegans
Q58704184	Loss of Bacitracin Resistance Due to a Large Genomic Deletion among Strains
Q90270583	Loss of Cx43 in Murine Sertoli Cells Leads to Altered Prepubertal Sertoli Cell Maturation and Impairment of the Mitosis-Meiosis Switch
Q92325664	Loss of DUX causes minor defects in zygotic genome activation and is compatible with mouse development
Q50942246	Loss of FAM46C Promotes Cell Survival in Myeloma.
Q33757192	Loss of Heterozygosity Drives Adaptation in Hybrid Yeast
Q88475996	Loss of KLHL6 promotes diffuse large B-cell lymphoma growth and survival by stabilizing the mRNA decay factor roquin2
Q93216454	Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood
Q27852894	Loss of NF1 in cutaneous melanoma is associated with RAS activation and MEK dependence
Q34677727	Loss of PHD3 allows tumours to overcome hypoxic growth inhibition and sustain proliferation through EGFR.
Q92264584	Loss of RNA Chaperone Hfq Unveils a Toxic Pathway in Pseudomonas aeruginosa
Q90205004	Loss of SATB1 Induces p21-Dependent Cellular Senescence in Post-mitotic Dopaminergic Neurons
Q34637394	Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy
Q89748170	Loss of glucocorticoid receptor expression mediates in vivo dexamethasone resistance in T-cell acute lymphoblastic leukemia
Q35731663	Loss of heterozygosity: what is it good for?
Q89820781	Loss-of-Function Mutation of Soybean R2R3 MYB Transcription Factor Dilutes Tawny Pubescence Color
Q37153028	Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling
Q33904619	Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease
Q47745542	Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes
Q35296003	Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene
Q36104839	Low Input Whole-Exome Sequencing to Determine the Representation of the Tumor Exome in Circulating DNA of Non-Small Cell Lung Cancer Patients
Q36021163	Low Mutation Burden in Ovarian Cancer May Limit the Utility of Neoantigen-Targeted Vaccines.
Q48354684	Low PTEN levels and PIK3CA mutations predict resistance to neoadjuvant lapatinib and trastuzumab without chemotherapy in patients with HER2 over-expressing breast cancer.
Q64081707	Low genetic variation is associated with low mutation rate in the giant duckweed
Q91235855	Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy - a pilot study
Q93010782	Low-Input MNase Accessibility of Chromatin (Low-Input MACC)
Q35180364	Low-grade prostate cancer diverges early from high grade and metastatic disease
Q55509938	Low-level mitochondrial heteroplasmy modulates DNA replication, glucose metabolism and lifespan in mice.
Q97517796	Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions
Q41981114	Lung neuroendocrine tumours: deep sequencing of the four World Health Organization histotypes reveals chromatin-remodelling genes as major players and a prognostic role for TERT, RB1, MEN1 and KMT2D.
Q48050366	Lyplal1 is dispensable for normal fat deposition in mice
Q56960691	Lysine benzoylation is a histone mark regulated by SIRT2
Q103805532	Lysine demethylase 7a regulates murine anterior-posterior development by modulating the transcription of Hox gene cluster
Q35731994	MAC: identifying and correcting annotation for multi-nucleotide variations
Q37146906	MADS-Box Transcription Factor VdMcm1 Regulates Conidiation, Microsclerotia Formation, Pathogenicity, and Secondary Metabolism of Verticillium dahliae
Q41929231	MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulation.
Q38671417	MED12 regulates a transcriptional network of calcium-handling genes in the heart.
Q88636857	MEF2‑activated long non‑coding RNA PCGEM1 promotes cell proliferation in hormone‑refractory prostate cancer through downregulation of miR‑148a
Q37702041	MET expression and copy number status in clear-cell renal cell carcinoma: prognostic value and potential predictive marker
Q34436309	MGAviewer: a desktop visualization tool for analysis of metagenomics alignment data
Q100633139	MIR2111-5 locus and shoot-accumulated mature miR2111 systemically enhance nodulation depending on HAR1 in Lotus japonicus
Q64263869	MITE , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in ATCC 17978 and Its Prevalence across the Family
Q56475859	MMARGE: Motif Mutation Analysis for Regulatory Genomic Elements
Q38981135	MNase-Sensitive Complexes in Yeast: Nucleosomes and Non-histone Barriers
Q91013991	MOWChIP-seq for low-input and multiplexed profiling of genome-wide histone modifications
Q47410836	MTA1 is a novel regulator of autophagy that induces tamoxifen resistance in breast cancer cells.
Q91770829	MTA2/NuRD Regulates B Cell Development and Cooperates with OCA-B in Controlling the Pre-B to Immature B Cell Transition
Q38659305	MUTATIONS IN THE E2 GLYCOPROTEIN AND THE 3' UNTRANSLATED REGION ENHANCE CHIKUNGUNYA VIRUS VIRULENCE IN MICE.
Q46456818	MYB transcription factor gene involved in sex determination in Asparagus officinalis.
Q34511655	MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism
Q39158975	MYCN and HDAC2 cooperate to repress miR-183 signaling in neuroblastoma
Q34662111	Magnetosome-containing bacteria living as symbionts of bivalves
Q40258088	Maintenance of the marginal-zone B cell compartment specifically requires the RNA-binding protein ZFP36L1.
Q33365211	Malate-dependent Fe accumulation is a critical checkpoint in the root developmental response to low phosphate
Q37049456	Male-specific region of the bovine Y chromosome is gene rich with a high transcriptomic activity in testis development
Q37248485	Mammary analog secretory carcinoma of the thyroid gland: A primary thyroid adenocarcinoma harboring ETV6-NTRK3 fusion
Q37546911	Mammary-specific gene activation is defined by progressive recruitment of STAT5 during pregnancy and the establishment of H3K4me3 marks
Q36286659	Manananggal - a novel viewer for alternative splicing events
Q92072795	Mapping Cucumber Vein Yellowing Virus Resistance in Cucumber (Cucumis sativus L.) by Using BSA-seq Analysis
Q37583703	Mapping Whole-Transcriptome Splicing in Mouse Hematopoietic Stem Cells.
Q46558029	Mapping genome-wide transcription-factor binding sites using DAP-seq.
Q36207245	Mapping of histone modifications in episomal HBV cccDNA uncovers an unusual chromatin organization amenable to epigenetic manipulation
Q35870178	Mapping the CgrA regulon of Rhodospirillum centenum reveals a hierarchal network controlling Gram-negative cyst development.
Q48021791	Mapping the malaria parasite druggable genome by using in vitro evolution and chemogenomics
Q35749827	Mapping vaccinia virus DNA replication origins at nucleotide level by deep sequencing
Q33920114	Mapping whole genome shotgun sequence and variant calling in mammalian species without their reference genomes
Q35325212	Mapsnp: an R package to plot a genomic map for single nucleotide polymorphisms
Q40974677	Massive Amplification at an Unselected Locus Accompanies Complex Chromosomal Rearrangements in Yeast
Q35911314	Massively parallel sequencing of phyllodes tumours of the breast reveals actionable mutations, and TERT promoter hotspot mutations and TERT gene amplification as likely drivers of progression
Q36889782	Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Q52375014	Massively parallel sequencing-enabled mixture analysis of mitochondrial DNA samples.
Q63406163	Maternal knockout causes loss of H3K27me3 imprinting and random X inactivation in the extraembryonic cells
Q90183071	Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals
Q83226945	Maternally regulated gastrulation as a source of variation contributing to cavefish forebrain evolution
Q53580017	Maxillary carcinosarcoma: Identification of a novel MET mutation in both carcinomatous and sarcomatous components through next generation sequencing.
Q92088409	McCune Albright syndrome is a genetic predisposition to intraductal papillary and mucinous neoplasms of the pancreas associated pancreatic cancer in relation with GNAS somatic mutation - a case report
Q90635259	MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2
Q34679937	Meander: visually exploring the structural variome using space-filling curves
Q40384168	Measuring microbial fitness in a field reciprocal transplant experiment
Q64081328	Measuring sequencer size bias using REcount: a novel method for highly accurate Illumina sequencing-based quantification
Q92823577	Mechanisms governing the pioneering and redistribution capabilities of the non-classical pioneer PU.1.
Q41627698	Mediator binds to boundaries of chromosomal interaction domains and to proteins involved in DNA looping, RNA metabolism, chromatin remodeling, and actin assembly.
Q30040534	Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations
Q33845382	Melanisation of Aspergillus terreus-Is Butyrolactone I Involved in the Regulation of Both DOPA and DHN Types of Pigments in Submerged Culture?
Q36793441	Melanoma adapts to RAF/MEK inhibitors through FOXD3-mediated upregulation of ERBB3
Q47566212	Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS.
Q91806520	Membrane metalloprotease TRABD2A restricts HIV-1 progeny production in resting CD4+ T cells by degrading viral Gag polyprotein
Q36181226	Membrane vesicle-mediated release of bacterial RNA
Q35584856	Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT): A Hybridization Capture-Based Next-Generation Sequencing Clinical Assay for Solid Tumor Molecular Oncology
Q64282939	Mendelian Inconsistent Signatures from 1314 Ancestrally Diverse Family Trios Distinguish Biological Variation from Sequencing Error
Q30695675	Mercadeo Virus: A Novel Mosquito-Specific Flavivirus from Panama
Q91874596	Merkel cell polyomavirus activates LSD1-mediated blockade of non-canonical BAF to regulate transformation and tumorigenesis
Q99415574	Merqury: reference-free quality, completeness, and phasing assessment for genome assemblies
Q90281640	Meta-analysis of Chromatin Programming by Steroid Receptors
Q47663049	Meta-analysis of transcriptomic datasets identifies genes enriched in the mammalian circadian pacemaker.
Q96815799	MetaRibo-Seq measures translation in microbiomes
Q89722307	Metabolic Labeling of RNAs Uncovers Hidden Features and Dynamics of the Arabidopsis Transcriptome
Q64981158	Metabolic heterogeneity underlies reciprocal fates of TH17 cell stemness and plasticity.
Q37131345	Metabolic reprogramming during neuronal differentiation from aerobic glycolysis to neuronal oxidative phosphorylation
Q63246383	Metagenomic Analysis Reveals Three Novel and Prevalent Mosquito Viruses from a Single Pool of Collected in the Republic of Korea
Q59351955	Metagenomic analysis of intestinal mucosa revealed a specific eukaryotic gut virome signature in early-diagnosed inflammatory bowel disease
Q55346790	Metagenomic analysis of viruses associated with maize lethal necrosis in Kenya.
Q30562554	Metagenomic shotgun sequencing of a Bunyavirus in wild-caught Aedes aegypti from Thailand informs the evolutionary and genomic history of the Phleboviruses
Q34091425	Metastatic tumor evolution and organoid modeling implicate TGFBR2 as a cancer driver in diffuse gastric cancer
Q41098443	Metformin inhibits SUV39H1-mediated migration of prostate cancer cells.
Q38812665	Methods, Tools and Current Perspectives in Proteogenomics
Q35391678	Methylation affects transposition and splicing of a large CACTA transposon from a MYB transcription factor regulating anthocyanin synthase genes in soybean seed coats
Q37126770	Methylation interactions in Arabidopsis hybrids require RNA-directed DNA methylation and are influenced by genetic variation
Q28533664	Methylation of histone H3 on lysine 79 associates with a group of replication origins and helps limit DNA replication once per cell cycle
Q35027111	Methylome analysis identifies a Wilms tumor epigenetic biomarker detectable in blood
Q34212632	Methylome, transcriptome, and PPAR(γ) cistrome analyses reveal two epigenetic transitions in fat cells
Q42425844	Mettl3-mediated m6A regulates spermatogonial differentiation and meiosis initiation.
Q34497810	MiR137 is an androgen regulated repressor of an extended network of transcriptional coregulators
Q34532230	Micro-scale genomic DNA copy number aberrations as another means of mutagenesis in breast cancer
Q35908632	MicroRNA genes and their target 3'-untranslated regions are infrequently somatically mutated in ovarian cancers
Q44733280	MicroRNA superfamilies descended from miR390 and their roles in secondary small interfering RNA Biogenesis in Eudicots
Q91728021	MicroRNA-196a is regulated by ER and is a prognostic biomarker in ER+ breast cancer
Q60046093	MicroRNA-31 Reduces the Motility of Proinflammatory T Helper 1 Lymphocytes
Q57128449	MicroRNA-532-5p Regulates Pericyte Function by Targeting the Transcription Regulator BACH1 and Angiopoietin-1
Q30578902	MicroScope--an integrated microbial resource for the curation and comparative analysis of genomic and metabolic data
Q35929472	Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing
Q37685585	Microevolution of Serial Clinical Isolates of Cryptococcus neoformans var. grubii and C. gattii
Q37130372	Microglandular adenosis associated with triple-negative breast cancer is a neoplastic lesion of triple-negative phenotype harbouring TP53 somatic mutations
Q93367738	Microsporidian Introns Retained against a Background of Genome Reduction: Characterization of an Unusual Set of Introns
Q36271668	Migration-related phenotypic divergence is associated with epigenetic modifications in rainbow trout
Q64117220	Mild inborn errors of metabolism in commonly used inbred mouse strains
Q89980485	Millefy: visualizing cell-to-cell heterogeneity in read coverage of single-cell RNA sequencing datasets
Q88639235	Minimap2: pairwise alignment for nucleotide sequences
Q47804286	Misidentification of genome assemblies in public databases: the case of Naumovozyma dairenensis and proposal of a protocol to correct misidentifications
Q92130375	Mismatched and wobble base pairs govern primary microRNA processing by human Microprocessor
Q27318452	Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed
Q64237918	Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2
Q64074125	Mitigating the effects of reference sequence bias in single-multiplex massively parallel sequencing of the mitochondrial DNA control region
Q28117404	Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates
Q89306618	Mitochondrial DNA Variation and Heteroplasmy in Monozygotic Twins Clinically Discordant for Multiple Sclerosis
Q27133880	Mitochondrial DNA from the eradicated European Plasmodium vivax and P. falciparum from 70-year-old slides from the Ebro Delta in Spain
Q39140349	Mitochondrial DNA sequence and phylogenetic evaluation of geographically disparate Sus scrofa breeds.
Q90638768	Mitochondrial Membrane Potential Regulates Nuclear Gene Expression in Macrophages Exposed to Prostaglandin E2
Q47243402	Mitochondrial Mutation Rate, Spectrum and Heteroplasmy in Caenorhabditis elegans Spontaneous Mutation Accumulation Lines of Differing Population Size
Q60907386	Mitochondrial RNA Expression and Single Nucleotide Variants in Association with Clinical Parameters in Primary Breast Cancers
Q90205302	Mitochondrial Reprogramming Underlies Resistance to BCL-2 Inhibition in Lymphoid Malignancies
Q34319499	Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations.
Q28834072	Mitochondrial genetic diversity, selection and recombination in a canine transmissible cancer
Q35022872	Mitochondrial sequence variation in African-American primary open-angle glaucoma patients
Q40250259	Mitochondrial transcripts and associated heteroplasmies of Ancistrus spp. (Siluriformes: Loricariidae).
Q41564634	Mitogenome Sequencing in the Genus Camelus Reveals Evidence for Purifying Selection and Long-term Divergence between Wild and Domestic Bactrian Camels
Q61610706	Mitogenome phylogeographic analysis of a planktonic crustacean
Q96027255	Mitogenomics reveals phylogenetic relationships of Arcoida (Mollusca, Bivalvia) and multiple independent expansions and contractions in mitochondrial genome size
Q43478776	Mitonuclear Interactions Mediate Transcriptional Responses to Hypoxia in Drosophila
Q35731450	MoSET1 (Histone H3K4 Methyltransferase in Magnaporthe oryzae) Regulates Global Gene Expression during Infection-Related Morphogenesis
Q35687336	Mobile element insertions are frequent in oesophageal adenocarcinomas and can mislead paired-end sequencing analysis
Q90275102	Modular Architecture of the STING C-Terminal Tail Allows Interferon and NF-κB Signaling Adaptation
Q92133904	Modulation of proliferation factors in lung adenocarcinoma with an analysis of the transcriptional consequences of genomic EGFR activation
Q50310624	Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
Q89992891	Molecular Basis of Cisplatin Resistance in Testicular Germ Cell Tumors
Q24288754	Molecular Characterisation of Chikungunya Virus Infections in Trinidad and Comparison of Clinical and Laboratory Features with Dengue and Other Acute Febrile Cases
Q55300517	Molecular Characterization and Putative Pathogenic Pathways of Tuberous Sclerosis Complex-Associated Renal Cell Carcinoma.
Q39965737	Molecular Diagnostics of Gliomas Using Next Generation Sequencing of a Glioma-Tailored Gene Panel
Q92255554	Molecular Signature of Subtypes of Non-Small-Cell Lung Cancer by Large-Scale Transcriptional Profiling: Identification of Key Modules and Genes by Weighted Gene Co-Expression Network Analysis (WGCNA)
Q52720328	Molecular Signatures of Regression of the Canine Transmissible Venereal Tumor.
Q57284937	Molecular alterations associated with metastases of solid pseudopapillary neoplasms of the pancreas
Q34493715	Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.
Q36849266	Molecular analysis of a male breast cancer patient with prolonged stable disease under mTOR/PI3K inhibitors BEZ235/everolimus.
Q55344702	Molecular basis of resistance to the microtubule-depolymerizing antitumor compound plocabulin.
Q34565756	Molecular characterization of serous ovarian carcinoma using a multigene next generation sequencing cancer panel approach
Q43906019	Molecular codes for cell type specification in Brn3 retinal ganglion cells.
Q91949069	Molecular effects of dADD1 misexpression in chromatin organization and transcription
Q35770202	Molecular evolution and in vitro characterization of Botryllus histocompatibility factor
Q37677296	Molecular evolution of the substrate utilization strategies and putative virulence factors in mosquito-associated Spiroplasma species.
Q47162598	Molecular genetic heterogeneity in undifferentiated endometrial carcinomas
Q50236911	Molecular genetics of coat colour variations in White Galloway and White Park cattle.
Q46244868	Molecular insights into the non-recombining nature of the spinach male-determining region.
Q37711802	Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1.
Q55448998	Molecular profiling and sequential somatic mutation shift in hypermutator tumours harbouring POLE mutations.
Q36106432	Molecular regulation of urea cycle function by the liver glucocorticoid receptor
Q36723436	Molecular shifts in limb identity underlie development of feathered feet in two domestic avian species.
Q35043965	Molecular typing of lung adenocarcinoma on cytological samples using a multigene next generation sequencing panel
Q36325186	Molecular, phenotypic, and sample-associated data to describe pluripotent stem cell lines and derivatives
Q37365501	Monitoring the immune response to vaccination with an inactivated vaccine associated to bovine neonatal pancytopenia by deep sequencing transcriptome analysis in cattle
Q99585652	Monosomic loss of MIR15A/MIR16-1 is a driver of multiple myeloma proliferation and disease progression
Q35833449	Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing
Q36932462	Mosaic genome structure of the barley powdery mildew pathogen and conservation of transcriptional programs in divergent hosts
Q31121767	Motif oriented high-resolution analysis of ChIP-seq data reveals the topological order of CTCF and cohesin proteins on DNA.
Q34774733	Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives
Q35160825	Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas
Q38848468	Multi-scale chromatin state annotation using a hierarchical hidden Markov model
Q48157504	Multicenter validation of cancer gene panel-based next-generation sequencing for translational research and molecular diagnostics.
Q55114672	Multilevel Differential Control of Hormone Gene Expression Programs by hnRNP L and LL in Pituitary Cells.
Q42101114	Multiple Components of the VHL Tumor Suppressor Complex Are Frequently Affected by DNA Copy Number Loss in Pheochromocytoma
Q38720377	Multiple Isoforms of Nesprin1 Are Integral Components of Ciliary Rootlets.
Q92999906	Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes
Q34597785	Multiple influenza A (H3N2) mutations conferring resistance to neuraminidase inhibitors in a bone marrow transplant recipient
Q88698646	Multiple large inversions and breakpoint rewiring of gene expression in the evolution of the fire ant social supergene
Q35740193	Multiple mechanisms of MYCN dysregulation in Wilms tumour
Q36640241	Multiple regulatory variants modulate expression of 5-hydroxytryptamine 2A receptors in human cortex
Q34336658	Multiple sex-associated regions and a putative sex chromosome in zebrafish revealed by RAD mapping and population genomics
Q30145570	Multiplex PCR method for MinION and Illumina sequencing of Zika and other virus genomes directly from clinical samples.
Q56990371	Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
Q35988901	Muscle cell identity requires Pax7-mediated lineage-specific DNA demethylation
Q97542491	MutCombinator: identification of mutated peptides allowing combinatorial mutations using nucleotide-based graph search
Q47557931	MutScan: fast detection and visualization of target mutations by scanning FASTQ data
Q48163413	Mutant KRAS Circulating Tumor DNA Is an Accurate Tool for Pancreatic Cancer Monitoring.
Q56889992	Mutant Variants of the Substrate-Binding Protein DppA from Escherichia coli Enhance Growth on Nonstandard γ-Glutamyl Amide-Containing Peptides
Q38818665	Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome.
Q45907873	Mutated ephrin receptor genes in non-small cell lung carcinoma and their occurrence with driver mutations-targeted resequencing study on formalin-fixed, paraffin-embedded tumor material of 81 patients.
Q52971846	Mutation Analysis of Cell-Free DNA and Single Circulating Tumor Cells in Metastatic Breast Cancer Patients with High Circulating Tumor Cell Counts.
Q36134488	Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
Q92715583	Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer
Q24629855	Mutation altering the miR-184 seed region causes familial keratoconus with cataract
Q60920322	Mutation analysis by deep sequencing of pancreatic juice from patients with pancreatic ductal adenocarcinoma
Q59421012	Mutation heterogeneity between primary gastric cancers and their matched lymph node metastases
Q31140340	Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype
Q37599744	Mutation in SNAP25 as a novel genetic cause of epilepsy and intellectual disability
Q52695037	Mutation in an alternative transcript of CDKL5 in a boy with early onset seizures.
Q36130881	Mutation mapping and identification by whole-genome sequencing
Q37688148	Mutation profiling of 19 candidate genes in acute myeloid leukemia suggests significance of DNMT3A mutations
Q37128670	Mutation rates, spectra, and genome-wide distribution of spontaneous mutations in mismatch repair deficient yeast
Q37560138	Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality
Q50137415	Mutational Profiling of Malignant Mesothelioma Revealed Potential Therapeutic Targets in EGFR and NRAS.
Q37098851	Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing
Q64386735	Mutational burden and signatures in 4,000 Japanese cancers provide insights into tumorigenesis and response to therapy
Q91662454	Mutational heterogeneity between different regional tumour grades of clear cell renal cell carcinoma
Q30665308	Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance.
Q37731513	Mutational patterns in the breast cancer mitochondrial genome, with clinical correlates
Q91855455	Mutational profile and EBV strains of extranodal NK/T-cell lymphoma, nasal type in Latin America
Q41437263	Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach
Q34654793	Mutational profiles in triple-negative breast cancer defined by ultradeep multigene sequencing show high rates of PI3K pathway alterations and clinically relevant entity subgroup specific differences
Q41299821	Mutational profiling of therapy-related myelodysplastic syndromes and acute myeloid leukemia by next generation sequencing, a comparison with de novo diseases
Q64262949	Mutational signatures and the genomic landscape of betel quid chewing-associated tongue carcinoma
Q52720227	Mutational signatures of DNA mismatch repair deficiency in C. elegans and human cancers.
Q43287348	Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis
Q36709030	Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.
Q91045801	Mutations in ASH1L confer susceptibility to Tourette syndrome
Q38870247	Mutations in Argonaute5 Illuminate Epistatic Interactions of the K1 and I Loci Leading to Saddle Seed Color Patterns in Glycine max.
Q33870601	Mutations in BRCA2 and taxane resistance in prostate cancer
Q37218536	Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis
Q30179423	Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
Q36595132	Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity
Q38965097	Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Q42428350	Mutations in KDSR Cause Recessive Progressive Symmetric Erythrokeratoderma
Q24293179	Mutations in PAX2 associate with adult-onset FSGS
Q57471565	Mutations in PERP cause dominant and recessive keratoderma
Q35168102	Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness.
Q29147466	Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
Q41975337	Mutations in TSC1, TSC2, and MTOR Are Associated with Response to Rapalogs in Patients with Metastatic Renal Cell Carcinoma
Q90370622	Mutations in a Novel Cadherin Gene Associated with Bt Resistance in Helicoverpa zea
Q100958822	Mutations in circulating tumor DNA predict primary resistance to systemic therapies in advanced hepatocellular carcinoma
Q35754537	Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Q28258055	Mutations in the NHEJ component XRCC4 cause primordial dwarfism
Q36106723	Mutations in the Plasmodium falciparum chloroquine resistance transporter, PfCRT, enlarge the parasite's food vacuole and alter drug sensitivities
Q36534922	Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm
Q35906678	Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.
Q42207007	Mutations in the neverland gene turned Drosophila pachea into an obligate specialist species
Q28115991	Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
Q58196742	Myc and the Tip60 chromatin remodeling complex control neuroblast maintenance and polarity in
Q36216328	Mycoplasma CG- and GATC-specific DNA methyltransferases selectively and efficiently methylate the host genome and alter the epigenetic landscape in human cells
Q90660624	Mylk3 null C57BL/6N mice develop cardiomyopathy, whereas Nnt null C57BL/6J mice do not
Q47664984	Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease.
Q37224867	Myristoylation of the Arenavirus Envelope Glycoprotein Stable Signal Peptide Is Critical for Membrane Fusion but Dispensable for Virion Morphogenesis
Q58589978	N-methyladenine DNA Modification in Glioblastoma
Q33771026	N-terminal Proteomics Assisted Profiling of the Unexplored Translation Initiation Landscape in Arabidopsis thaliana
Q28585513	N6-methyladenosine modification destabilizes developmental regulators in embryonic stem cells
Q72080559	N6-methyldeoxyadenine is a transgenerational epigenetic signal for mitochondrial stress adaptation
Q98196901	NAD tagSeq for transcriptome-wide identification and characterization of NAD+-capped RNAs
Q92381410	NAD tagSeq reveals that NAD+-capped RNAs are mostly produced from a large number of protein-coding genes in Arabidopsis
Q92132685	NCOR1 Orchestrates Transcriptional Landscapes and Effector Functions of CD4+ T Cells
Q35910335	NEAT: a framework for building fully automated NGS pipelines and analyses
Q38374543	NEBNext Direct: A Novel, Rapid, Hybridization-Based Approach for the Capture and Library Conversion of Genomic Regions of Interest
Q63976673	NF-κB upregulates glutamine-fructose-6-phosphate transaminase 2 to promote migration in non-small cell lung cancer
Q37286915	NF1 Mutations Are Common in Desmoplastic Melanoma
Q36273267	NF2 Loss Promotes Oncogenic RAS-Induced Thyroid Cancers via YAP-Dependent Transactivation of RAS Proteins and Sensitizes Them to MEK Inhibition
Q40046514	NFATc1 controls the cytotoxicity of CD8+ T cells
Q94563226	NFI transcription factors provide chromatin access to maintain stem cell identity while preventing unintended lineage fate choices
Q91907808	NFIA is a gliogenic switch enabling rapid derivation of functional human astrocytes from pluripotent stem cells
Q57536756	NGS Datenanalyse und Qualitätskontrolle
Q28278914	NGS analyses by visualization with Trackster
Q39222037	NGS for Sequence Variants
Q39373131	NGS-based reverse genetic screen for common embryonic lethal mutations compromising fertility in livestock.
Q31040461	NMFP: a non-negative matrix factorization based preselection method to increase accuracy of identifying mRNA isoforms from RNA-seq data
Q58615757	NOTCH1 pathway activating mutations and clonal evolution in pediatric T-cell acute lymphoblastic leukemia (T-ALL)
Q46257036	NRF2 regulates endothelial glycolysis and proliferation with miR-93 and mediates the effects of oxidized phospholipids on endothelial activation
Q91963132	Nanopore Targeted Sequencing for Rapid Gene Mutations Detection in Acute Myeloid Leukemia
Q83224631	Nanopore direct RNA sequencing maps the complexity of Arabidopsis mRNA processing and mA modification
Q50066036	Nanopore sequencing and assembly of a human genome with ultra-long reads.
Q47097491	Nanopore-based single molecule sequencing of the D4Z4 array responsible for facioscapulohumeral muscular dystrophy.
Q37379794	Nascent RNA sequencing reveals distinct features in plant transcription
Q90099983	Nascent transcript analysis of glucocorticoid crosstalk with TNF defines primary and cooperative inflammatory repression
Q35804162	Native promoter strategy for high-yielding synthesis and engineering of fungal secondary metabolites
Q35118800	Natural antisense transcripts and long non-coding RNA in Neurospora crassa
Q88159955	Natural occurring epialleles determine vitamin E accumulation in tomato fruits
Q37420349	Natural variation in the histone demethylase, KDM4C, influences expression levels of specific genes including those that affect cell growth
Q55247742	Naturally occurring a loss of a giant plasmid from Mycobacterium ulcerans subsp. shinshuense makes it non-pathogenic.
Q35742680	Nbs1 ChIP-Seq Identifies Off-Target DNA Double-Strand Breaks Induced by AID in Activated Splenic B Cells
Q34249505	Negative regulation of the interferon response by an interferon-induced long non-coding RNA
Q90648479	Neoantigen vaccine generates intratumoral T cell responses in phase Ib glioblastoma trial
Q92332582	Neoantigen-specific immunity in low mutation burden colorectal cancers of the consensus molecular subtype 4
Q92513287	Nested retrotransposition in the East Asian mouse genome causes the classical nonagouti mutation
Q61806912	Neuroblast-specific open chromatin allows the temporal transcription factor, Hunchback, to bind neuroblast-specific loci
Q99557388	Neurological disorder-associated genetic variants in individuals with psychogenic nonepileptic seizures
Q42319910	Neuronal activity modifies the chromatin accessibility landscape in the adult brain
Q27311371	Neurospora importin α is required for normal heterochromatic formation and DNA methylation
Q89822372	Neurotrophic Receptor Tyrosine Kinase 2 (NTRK2) Alterations in Low-Grade Gliomas: Report of a Novel Gene Fusion Partner in a Pilocytic Astrocytoma and Review of the Literature
Q34515911	New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Q90011543	New Insights Into Chromomere Organization Provided by Lampbrush Chromosome Microdissection and High-Throughput Sequencing
Q35758656	New Noncoding Lytic Transcripts Derived from the Epstein-Barr Virus Latency Origin of Replication, oriP, Are Hyperedited, Bind the Paraspeckle Protein, NONO/p54nrb, and Support Viral Lytic Transcription
Q30317031	New gene models and alternative splicing in the maize pathogen Colletotrichum graminicola revealed by RNA-Seq analysis
Q52606771	New insights into the phylogenetics and population structure of the prairie falcon (Falco mexicanus).
Q34530586	New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre
Q54525480	Newborn Screening Quality Assurance Program for CFTR Mutation Detection and Gene Sequencing to Identify Cystic Fibrosis.
Q49893515	Newly designed 11-gene panel reveals first case of hereditary amyloidosis captured by massive parallel sequencing.
Q100761896	Newly established gastrointestinal cancer cell lines retain the genomic and immunophenotypic landscape of their parental cancers
Q92239134	Next Generation DNA-Seq and Differential RNA-Seq Allow Re-annotation of the Pyrococcus furiosus DSM 3638 Genome and Provide Insights Into Archaeal Antisense Transcription
Q40427450	Next Generation Sequencing of Circulating Cell-Free DNA for Evaluating Mutations and Gene Amplification in Metastatic Breast Cancer
Q38014423	Next generation quantitative genetics in plants
Q34941781	Next generation sequencing analysis of nine Corynebacterium ulcerans isolates reveals zoonotic transmission and a novel putative diphtheria toxin-encoding pathogenicity island
Q90390596	Next generation sequencing as second-tier test in high-throughput newborn screening for nephropathic cystinosis
Q34242488	Next generation sequencing for molecular diagnosis of neuromuscular diseases.
Q55668666	Next generation sequencing identifies novel disease-associated BEST1 mutations in Bestrophinopathy patients.
Q36429570	Next generation sequencing of CLU, PICALM and CR1: pitfalls and potential solutions.
Q91533544	Next generation sequencing of the cellular and liquid fraction of pancreatic cyst fluid supports discrimination of IPMN from pseudocysts and reveals cases with multiple mutated driver clones: First findings from the prospective ZYSTEUS biomarker stu
Q58760165	Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia
Q41919817	Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability
Q30448812	Next-generation sequence analysis of cancer xenograft models.
Q38817647	Next-generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters
Q35600008	Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl(-/-) retinal transcriptomes.
Q34238930	Next-generation sequencing for cancer diagnostics: a practical perspective.
Q64886567	Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.
Q42330162	Next-generation sequencing identifies major DNA methylation changes during progression of Ph+ chronic myeloid leukemia
Q33866887	Next-generation sequencing of circulating tumor DNA to predict recurrence in triple-negative breast cancer patients with residual disease after neoadjuvant chemotherapy
Q34460796	Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints
Q40275671	Next-generation sequencing of urine specimens: A novel platform for genomic analysis in patients with non-muscle-invasive urothelial carcinoma treated with bacille Calmette-Guérin.
Q36963020	Next-generation sequencing reveals somatic mutations that confer exceptional response to everolimus.
Q38242485	Next-generation sequencing technologies: breaking the sound barrier of human genetics
Q88805473	Next-generation sequencing unravels extensive genetic alteration in recurrent ovarian cancer and unique genetic changes in drug-resistant recurrent ovarian cancer
Q91590370	Next-generation sequencing with comprehensive bioinformatics analysis facilitates somatic mosaic APC gene mutation detection in patients with familial adenomatous polyposis
Q37618897	Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring
Q38029472	Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders
Q37126113	Niakha virus: a novel member of the family Rhabdoviridae isolated from phlebotomine sandflies in Senegal
Q57169170	Nimbus: a design-driven analyses suite for amplicon-based NGS data
Q39387886	Nitrogen cost minimization is promoted by structural changes in the transcriptome of N-deprived Prochlorococcus cells
Q59410000	No Evidence for Recent Selection at FOXP2 among Diverse Human Populations
Q90613270	No evidence for DNA N 6-methyladenine in mammals
Q92875175	Non-canonical translation initiation in yeast generates a cryptic pool of mitochondrial proteins
Q33807980	Non-invasive analysis of intestinal development in preterm and term infants using RNA-Sequencing
Q38804360	Non-invasive pre-implantation aneuploidy screening and diagnosis of beta thalassemia IVSII654 mutation using spent embryo culture medium
Q48150902	Non-invasive prenatal diagnosis of beta-thalassemia by semiconductor sequencing: a feasibility study in the sardinian population.
Q93000933	Nonallelic homologous recombination events responsible for copy number variation within an RNA silencing locus
Q92093980	Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
Q89601690	Noncoding RNA transcription alters chromosomal topology to promote isotype-specific class switch recombination
Q33421975	Noninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing
Q38843246	Nonoverlapping Clinical and Mutational Patterns in Melanomas from the Female Genital Tract and Atypical Genital Nevi.
Q33865160	Nonrandom domain organization of the Arabidopsis genome at the nuclear periphery.
Q47198829	Nonsense mRNA suppression via nonstop decay
Q41928299	Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome
Q37549988	Normal chromosome conformation depends on subtelomeric facultative heterochromatin in Neurospora crassa
Q28468650	Notch pathway activation is essential for maintenance of stem-like cells in early tongue cancer
Q51019461	Novel Androgen Receptor Coregulator GRHL2 Exerts Both Oncogenic and Antimetastatic Functions in Prostate Cancer.
Q36231506	Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing
Q97420676	Novel Erwinia persicina Infecting Phage Midgardsormr38 Within the Context of Temperate Erwinia Phages
Q98465808	Novel FANCA mutation in the first fully-diagnosed patient with Fanconi anemia in Polish population - case report
Q36957976	Novel Meiotic miRNAs and Indications for a Role of PhasiRNAs in Meiosis.
Q38545042	Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis
Q34498285	Novel RNA variants in colorectal cancers
Q37543423	Novel RpoS-Dependent Mechanisms Strengthen the Envelope Permeability Barrier during Stationary Phase
Q28550077	Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy
Q102141661	Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort
Q35670523	Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome
Q90683251	Novel approach in whole genome mining and transcriptome analysis reveal conserved RiPPs in Trichoderma spp
Q44457947	Novel cases of D-2-hydroxyglutaric aciduria with IDH1 or IDH2 mosaic mutations identified by amplicon deep sequencing
Q37466323	Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS, in a Finnish family
Q92628738	Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global developmental delay
Q58695957	Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition
Q52664082	Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report.
Q46161183	Novel hydrocarbon monooxygenase genes in the metatranscriptome of a natural deep-sea hydrocarbon plume
Q38620814	Novel landscape of HLA-G isoforms expressed in clear cell renal cell carcinoma patients.
Q38909020	Novel long non-coding RNAs are specific diagnostic and prognostic markers for prostate cancer
Q99554359	Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy
Q30363402	Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome.
Q55070034	Novel oncogene and tumor suppressor mutations in KIT and PDGFRA wild type gastrointestinal stromal tumors revealed by next generation sequencing.
Q28828711	Novel small molecules potentiate premature termination codon readthrough by aminoglycosides
Q36524711	Novel somatic mutations identified by whole-exome sequencing in muscle-invasive transitional cell carcinoma of the bladder
Q55110051	Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophy.
Q37072396	Novel variation at chr11p13 associated with cystic fibrosis lung disease severity.
Q64106792	Novel, rare and common pathogenic variants in the CFTR gene screened by high-throughput sequencing technology and predicted by in silico tools
Q60960906	NovoGraph: Human genome graph construction from multiple long-read assemblies
Q33726837	Nrf2 amplifies oxidative stress via induction of Klf9.
Q98192776	NuRD subunit CHD4 regulates super-enhancer accessibility in Rhabdomyosarcoma and represents a general tumor dependency
Q41003407	NucDiff: in-depth characterization and annotation of differences between two sets of DNA sequences.
Q51041546	Nuclear Proximity of Mtr4 to RNA Exosome Restricts DNA Mutational Asymmetry.
Q58610257	Nuclear Transcriptomes of the Seven Neuronal Cell Types That Constitute the Mushroom Bodies
Q35620895	Nuclear hormone 1α,25-dihydroxyvitamin D3 elicits a genome-wide shift in the locations of VDR chromatin occupancy
Q91738845	Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans
Q97569214	Nucleolar RNA polymerase II drives ribosome biogenesis
Q33669370	Nucleomorph and plastid genome sequences of the chlorarachniophyte Lotharella oceanica: convergent reductive evolution and frequent recombination in nucleomorph-bearing algae
Q90561193	Nucleosome Positioning by an Evolutionarily Conserved Chromatin Remodeler Prevents Aberrant DNA Methylation in Neurospora
Q89665043	Nucleosome destabilization by nuclear non-coding RNAs
Q33791130	Nucleosome eviction and multiple co-factor binding predict estrogen-receptor-alpha-associated long-range interactions
Q35140349	Nucleosomes are stably evicted from enhancers but not promoters upon induction of certain pro-inflammatory genes in mouse macrophages
Q90754874	Nucleotide resolution profiling of m7G tRNA modification by TRAC-Seq
Q90561758	NusG prevents transcriptional invasion of H-NS-silenced genes
Q58778244	O-GlcNAcylation Signal Mediates Proteasome Inhibitor Resistance in Cancer Cells by Stabilizing NRF1
Q46562922	OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps.
Q46450555	OR2M3: A Highly Specific and Narrowly Tuned Human Odorant Receptor for the Sensitive Detection of Onion Key Food Odorant 3-Mercapto-2-methylpentan-1-ol.
Q64245811	ORAI1 and ORAI3 in Breast Cancer Molecular Subtypes and the Identification of ORAI3 as a Hypoxia Sensitive Gene and a Regulator of Hypoxia Responses
Q30819731	OTG-snpcaller: an optimized pipeline based on TMAP and GATK for SNP calling from ion torrent data
Q38755960	OTX2 Activity at Distal Regulatory Elements Shapes the Chromatin Landscape of Group 3 Medulloblastoma
Q94456293	OTX2 represses sister cell fate choices in the developing retina to promote photoreceptor specification
Q91272389	Obesity is associated with altered gene expression in human tastebuds
Q50113678	Octopus-toolkit: a workflow to automate mining of public epigenomic and transcriptomic next-generation sequencing data.
Q57800211	Oligodendrocyte differentiation of induced pluripotent stem cells derived from subjects with schizophrenias implicate abnormalities in development
Q46299533	Omics approaches to study gene regulatory networks for development in echinoderms
Q47660956	Onco-proteogenomics: Multi-omics level data integration for accurate phenotype prediction
Q60955781	Oncogenic is differentially regulated in wild-type vs. mutant gliomas
Q92474367	Oncogenic splicing abnormalities induced by DEAD-Box Helicase 56 amplification in colorectal cancer
Q36937377	Optimization of CRISPR/Cas9 genome editing to modify abiotic stress responses in plants
Q35390275	Optimization of the genotyping-by-sequencing strategy for population genomic analysis in conifers.
Q51147289	Optimized Method of Extracting Rice Chloroplast DNA for High-Quality Plastome Resequencing and de Novo Assembly.
Q48138460	Optimized targeted sequencing of cell-free plasma DNA from bladder cancer patients.
Q50058933	Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice.
Q90754750	Organoid single-cell genomic atlas uncovers human-specific features of brain development
Q37197994	Orientation-specific RAG activity in chromosomal loop domains contributes to Tcrd V(D)J recombination during T cell development
Q47249668	Orthogonality and Burdens of Heterologous AND Gate Gene Circuits in E. coli
Q58750471	Orthologous Genes in spp. Shed Light on a Noteworthy NBS-LRR Cluster Conferring Differential Resistance to Root-Knot Nematodes
Q92467391	OsNAC2 integrates auxin and cytokinin pathways to modulate rice root development
Q91998435	OsbZIP81, A Homologue of Arabidopsis VIP1, May Positively Regulate JA Levels by Directly Targetting the Genes in JA Signaling and Metabolism Pathway in Rice
Q36008016	Ostreococcus tauri is a new model green alga for studying iron metabolism in eukaryotic phytoplankton
Q40056614	Outbreak of Zika Virus Infection, Chiapas State, Mexico, 2015, and First Confirmed Transmission by Aedes aegypti Mosquitoes in the Americas
Q91910292	Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders
Q28543021	Ovarian cancer cell line panel (OCCP): clinical importance of in vitro morphological subtypes
Q36426409	Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry
Q48896342	Overcoming the membrane barrier: Recruitment of γ-glutamyl transferase for intracellular release of metabolic cargo from peptide vectors.
Q64092997	P-TEFb Regulates Transcriptional Activation in Non-coding RNA Genes
Q35602226	PAPST, a User Friendly and Powerful Java Platform for ChIP-Seq Peak Co-Localization Analysis and Beyond
Q50053227	PARIS: Psoralen Analysis of RNA Interactions and Structures with High Throughput and Resolution.
Q58693148	PARP1 Stabilizes CTCF Binding and Chromatin Structure To Maintain Epstein-Barr Virus Latency Type
Q91045688	PAX5-driven subtypes of B-progenitor acute lymphoblastic leukemia
Q37544968	PAX6 maintains β cell identity by repressing genes of alternative islet cell types
Q31155306	PBrowse: a web-based platform for real-time collaborative exploration of genomic data.
Q93133611	PIF transcription factors link a neighbor threat cue to accelerated reproduction in Arabidopsis
Q37010421	PIK3R1 mutations cause syndromic insulin resistance with lipoatrophy
Q64102234	PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population
Q89790354	PIWI-piRNA pathway-mediated transposable element repression in Hydra somatic stem cells
Q64072072	PLZF limits enhancer activity during hematopoietic progenitor aging
Q38877286	PML protein organizes heterochromatin domains where it regulates histone H3.3 deposition by ATRX/DAXX.
Q35074751	POMO--Plotting Omics analysis results for Multiple Organisms
Q37534124	POWERDRESS and HDA9 interact and promote histone H3 deacetylation at specific genomic sites in Arabidopsis
Q49972333	PRC2 Is Dispensable in Vivo for β-Catenin-Mediated Repression of Chondrogenesis in the Mouse Embryonic Cranial Mesenchyme.
Q92479395	PRC2-Mediated H3K27me3 Contributes to Transcriptional Regulation of FIT-Dependent Iron Deficiency Response
Q96773639	PRC2-mediated H3K27me3 modulates shoot iron homeostasis in Arabidopsis thaliana
Q34492529	PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
Q37417059	PRMT5-mediated histone H4 arginine-3 symmetrical dimethylation marks chromatin at G + C-rich regions of the mouse genome
Q36392900	PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss
Q63979688	PTBP1-Mediated Alternative Splicing Regulates the Inflammatory Secretome and the Pro-tumorigenic Effects of Senescent Cells
Q29999309	Pacific biosciences sequencing technology for genotyping and variation discovery in human data
Q89529208	Painting of Fourth and the X-Linked 1.688 Satellite in D. melanogaster is Involved in Chromosome-Wide Gene Regulation
Q38646960	Pancreatic intraductal tubulopapillary neoplasm is genetically distinct from intraductal papillary mucinous neoplasm and ductal adenocarcinoma
Q89055048	Paneth Cell Multipotency Induced by Notch Activation following Injury
Q42097429	Panoptes: web-based exploration of large scale genome variation data
Q27336499	ParA and ParB coordinate chromosome segregation with cell elongation and division during Streptomyces sporulation.
Q36983096	Parallel Evolution in Streptococcus pneumoniae Biofilms.
Q90371851	Parallel evolution of dominant pistil-side self-incompatibility suppressors in Arabidopsis
Q34130250	Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed
Q39558408	Parallel targeted next generation sequencing of childhood and adult acute myeloid leukemia patients reveals uniform genomic profile of the disease
Q40045106	Parasex Generates Phenotypic Diversity de Novo and Impacts Drug Resistance and Virulence in Candida albicans
Q93050672	Parent-of-origin-specific allelic expression in the human placenta is limited to established imprinted loci and it is stably maintained across pregnancy
Q94590016	Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings
Q64799902	Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.
Q47435196	Partial bisulfite conversion for unique template sequencing
Q96172025	Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing
Q64890831	Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspring.
Q37971380	Pathogen comparative genomics in the next-generation sequencing era: genome alignments, pangenomics and metagenomics.
Q89837929	Pathogen-associated Molecular Pattern-triggered Immunity Involves Proteolytic Degradation of Core Nonsense-mediated mRNA Decay Factors During the Early Defense Response
Q64120750	Pathogenic Gene Mutations or Variants Identified by Targeted Gene Sequencing in Adults With Hemophagocytic Lymphohistiocytosis
Q52602399	Pathogenic Germline Variants in 10,389 Adult Cancers.
Q93133432	Patient-derived lung cancer organoids as in vitro cancer models for therapeutic screening
Q48097679	Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities
Q92205128	PattRec: An easy-to-use CNV detection tool optimized for targeted NGS assays with diagnostic purposes
Q53077833	Patterns of alternative splicing vary between species during heat stress.
Q35161248	Patterns of genome-wide VDR locations.
Q35146248	Patterns of homoeologous gene expression shown by RNA sequencing in hexaploid bread wheat.
Q51075293	Patterns of stress response and tolerance based on transcriptome profiling of rice crown tissue under zinc deficiency.
Q37246199	Pax6 associates with H3K4-specific histone methyltransferases Mll1, Mll2, and Set1a and regulates H3K4 methylation at promoters and enhancers
Q42156236	Pbx and Prdm1a transcription factors differentially regulate subsets of the fast skeletal muscle program in zebrafish
Q47866088	Pediatric Cystic Nephroma Is Morphologically, Immunohistochemically, and Genetically Distinct From Adult Cystic Nephroma
Q90424017	Pedigree-based estimation of human mobile element retrotransposition rates
Q37376636	Pentatricopeptide repeat 336 as the candidate gene for paternal sorting of mitochondria (Psm) in cucumber.
Q38833997	Performance characteristics of the AmpliSeq Cancer Hotspot panel v2 in combination with the Ion Torrent Next Generation Sequencing Personal Genome Machine
Q34987476	Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing
Q30375683	Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing.
Q55071303	Performance of amplicon-based next generation DNA sequencing for diagnostic gene mutation profiling in oncopathology.
Q50057282	Performance of the Early Access AmpliSeq™ Mitochondrial Panel with degraded DNA samples using the Ion Torrent™ platform.
Q55738656	Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes
Q92148977	Pergola-web: a web server for the visualization and analysis of longitudinal behavioral data using repurposed genomics tools and standards
Q59136881	Pergola: Boosting Visualization and Analysis of Longitudinal Data by Unlocking Genomic Analysis Tools
Q36980908	Peripheral blood methylation profiling of female Crohn's disease patients
Q91832362	Peroxisomal β-oxidation regulates histone acetylation and DNA methylation in Arabidopsis
Q37338371	Persistence of DNMT3A R882 mutations during remission does not adversely affect outcomes of patients with acute myeloid leukaemia
Q61803964	Persistent mutations in remission can predict relapse in patients with acute myeloid leukemia
Q38113052	Perspectives for identification of mutations in the zebrafish: making use of next-generation sequencing technologies for forward genetic approaches
Q58617453	Pervasive Gene Conversion in Chromosomal Inversion Heterozygotes
Q34358875	Pervasive genetic hitchhiking and clonal interference in forty evolving yeast populations
Q40055659	Pf16 and phiPMW: Expanding the realm of Pseudomonas putida bacteriophages.
Q48164512	Phacomatosis pigmentokeratotica and precocious puberty associated with HRAS mutation
Q47128891	Pharmacogenetic Variation in Over 100 Genes in Patients Receiving Acenocumarol
Q47665232	Pharmacogenetic determinants of outcomes on triplet hepatic artery infusion and intravenous cetuximab for liver metastases from colorectal cancer (European trial OPTILIV, NCT00852228).
Q90114151	Phase 2 clinical trial of TORC1 inhibition with everolimus in men with metastatic castration-resistant prostate cancer
Q37598084	Phase II trial of MEK inhibitor selumetinib (AZD6244, ARRY-142886) in patients with BRAFV600E/K-mutated melanoma.
Q42320461	Phase variable DNA repeats in Neisseria gonorrhoeae influence transcription, translation, and protein sequence variation
Q49791467	Phenazines regulate Nap-dependent denitrification in Pseudomonas aeruginosa biofilms.
Q35196159	Phenotype specific analyses reveal distinct regulatory mechanism for chronically activated p53
Q49691357	Phenotype-based gene analysis allowed successful diagnosis of X-linked neutropenia associated with a novel WASp mutation.
Q91775571	Phenotypic and Genotypic Consequences of CRISPR/Cas9 Editing of the Replication Origins in the rDNA of Saccharomyces cerevisiae
Q33699514	Pheromone independent unisexual development in Cryptococcus neoformans
Q64296067	Phloem Companion Cell-Specific Transcriptomic and Epigenomic Analyses Identify MRF1, a Regulator of Flowering
Q37150720	Phorbol ester-mediated re-expression of endogenous LAT adapter in J.CaM2 cells: a model for dissecting drivers and blockers of LAT transcription.
Q38716411	Phosphatidylinositol 3-kinase δ blockade increases genomic instability in B cells
Q35843428	Phosphodiesterase sequence variants may predispose to prostate cancer
Q92451853	Phosphorylation of histone H3.3 at serine 31 promotes p300 activity and enhancer acetylation
Q64108803	Phylogenetic Analyses and GAGA-Motif Binding Studies of BBR/BPC Proteins Lend to Clues in GAGA-Motif Recognition and a Regulatory Role in Brassinosteroid Signaling
Q59350063	Phylogenetic analysis of West Nile Virus in Maricopa County, Arizona: Evidence for dynamic behavior of strains in two major lineages in the American Southwest
Q36327058	Phylogenomic inferences from reference-mapped and de novo assembled short-read sequence data using RADseq sequencing of California white oaks (Quercus section Quercus).
Q91723664	Physcomitrella STEMIN transcription factor induces stem cell formation with epigenetic reprogramming
Q37371035	Phytohormone sensing in the biotrophic fungus Ustilago maydis - the dual role of the transcription factor Rss1.
Q56962327	PiGx: Reproducible genomics analysis pipelines with GNU Guix
Q92636301	Pigment Intensity in Dogs is Associated with a Copy Number Variant Upstream of KITLG
Q35075704	PileLineGUI: a desktop environment for handling genome position files in next-generation sequencing studies
Q35997083	Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution
Q93095364	Pinpointing the Genomic Localizations of Chromatin-Associated Proteins: The Yesterday, Today, and Tomorrow of ChIP-seq
Q61445680	Piwi-interacting RNA (piRNA) expression patterns in pearl oyster (Pinctada fucata) somatic tissues
Q94591986	Plant 22-nt siRNAs mediate translational repression and stress adaptation
Q93053251	Plant HP1 protein ADCP1 links multivalent H3K9 methylation readout to heterochromatin formation
Q44746315	Plant genetics. A Y-chromosome-encoded small RNA acts as a sex determinant in persimmons.
Q93271158	Plasma cell-free DNA variant analysis compared with methylated DNA analysis in renal cell carcinoma
Q39337417	Plasmablastic lymphoma phenotype is determined by genetic alterations in MYC and PRDM1.
Q30043631	Plasmodium falciparum Maf1 Confers Survival upon Amino Acid Starvation
Q46796228	Plasticity of the MFS1 Promoter Leads to Multidrug Resistance in the Wheat Pathogen Zymoseptoria tritici
Q91044969	Plasticity of the Mycobacterium tuberculosis respiratory chain and its impact on tuberculosis drug development
Q37661601	Playing hide and seek with repeats in local and global de novo transcriptome assembly of short RNA-seq reads
Q39649075	PoPoolation2: identifying differentiation between populations using sequencing of pooled DNA samples (Pool-Seq)
Q28485193	Polyadenylation-dependent control of long noncoding RNA expression by the poly(A)-binding protein nuclear 1
Q59129666	Polyamine flux suppresses histone lysine demethylases and enhances expression in cancer stem cells
Q37528887	Polycomb recruitment attenuates retinoic acid-induced transcription of the bivalent NR2F1 gene
Q47402982	Polycomb repression complex 2 is required for the maintenance of retinal progenitor cells and balanced retinal differentiation
Q56981739	Polymorphic NumtS trace human population relationships
Q91603926	Polymorphism analyses and protein modelling inform on functional specialization of Piwi clade genes in the arboviral vector Aedes albopictus
Q91868424	Polymorphisms in the Mitochondrial Genome Are Associated With Bullous Pemphigoid in Germans
Q40909162	PopGeV: a web-based large-scale population genome browser
Q90226616	Population Genomic Approaches for Weed Science
Q58103165	Population data improves variant interpretation in autosomal dominant polycystic kidney disease
Q38518806	Population divergence in the wheat leaf rust fungus Puccinia triticina is correlated with wheat evolution
Q33694358	Population genomics reveals a candidate gene involved in bumble bee pigmentation
Q33725460	Populations of latent Mycobacterium tuberculosis lack a cell wall: Isolation, visualization, and whole-genome characterization
Q101226579	Portuguese wild grapevine genome re-sequencing (Vitis vinifera sylvestris)
Q55222848	Positive selection inhibits gene mobilisation and transfer in soil bacterial communities.
Q92392997	Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
Q28817439	Post-polyploidisation morphotype diversification associates with gene copy number variation
Q37091663	Post-transcriptional regulation of myotube elongation and myogenesis by Hoi Polloi
Q28263098	Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation
Q53368622	Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.
Q34523721	Posttranscriptional m(6)A Editing of HIV-1 mRNAs Enhances Viral Gene Expression.
Q37604396	Potential molecular consequences of transgene integration: The R6/2 mouse example
Q92996654	Potential prognostic impact of EBV RNA-seq reads in gastric cancer: a reanalysis of The Cancer Genome Atlas cohort
Q102075430	Potential virus-mediated nitrogen cycling in oxygen-depleted oceanic waters
Q35998917	Practical Guidelines for High-Resolution Epigenomic Profiling of Nucleosomal Histones in Postmortem Human Brain Tissue.
Q21563477	Practical guidelines for the comprehensive analysis of ChIP-seq data
Q55456692	Practical implementation of DNA methylation and copy-number-based CNS tumor diagnostics: the Heidelberg experience.
Q49538593	Precise genome-wide mapping of single nucleosomes and linkers in vivo.
Q64039613	Precise therapeutic gene correction by a simple nuclease-induced double-stranded break
Q88653167	Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory
Q92561302	Precursors for Nonlymphoid-Tissue Treg Cells Reside in Secondary Lymphoid Organs and Are Programmed by the Transcription Factor BATF
Q39610520	Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation
Q101403141	Prediction of mitochondrial genome-wide variation through sequencing of mitochondrion-enriched extracts
Q92085561	Prediction of regulatory long intergenic non-coding RNAs acting in trans through base-pairing interactions
Q90099730	Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6
Q103002671	Premature termination codons in SOD1 causing Amyotrophic Lateral Sclerosis are predicted to escape the nonsense-mediated mRNA decay
Q50002764	Prenatal Exposure to Bisphenol A Disrupts Naturally Occurring Bimodal DNA Methylation at Proximal Promoter of fggy, an Obesity-Relevant Gene Encoding a Carbohydrate Kinase, in Gonadal White Adipose Tissues of CD-1 Mice.
Q33616987	Prenatal Exposure to a Maternal High-Fat Diet Affects Histone Modification of Cardiometabolic Genes in Newborn Rats.
Q42092692	Prepatterning of differentiation-driven nuclear lamin A/C-associated chromatin domains by GlcNAcylated histone H2B.
Q36581642	Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients
Q93156065	Previously Identified Genetic Variants in ADGRL3 Are not Associated with Risk for Equine Degenerative Myeloencephalopathy across Breeds
Q37130539	Primary cancer cell culture: mammary-optimized vs conditional reprogramming
Q39303726	Primary familial brain calcification linked to deletion of 5' noncoding region of SLC20A2.
Q64109922	Primed histone demethylation regulates shoot regenerative competency
Q37225762	Principles for RNA metabolism and alternative transcription initiation within closely spaced promoters
Q91647462	Probabilistic model based on circular statistics for quantifying coverage depth dynamics originating from DNA replication
Q60912408	Probe-based association analysis identifies several deletions associated with average daily gain in beef cattle
Q28662023	Probing bacterial metabolism during infection using high-resolution transcriptomics
Q40492436	Profiling New Small RNA Sequences
Q40295360	Profiling and Characterization of Small RNAs in the Liverwort, Marchantia polymorpha, Belonging to the First Diverged Land Plants
Q88571278	Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes
Q47694712	Profiling of Single-Cell Transcriptomes
Q64067794	Profiling of chromatin accessibility and identification of general cis-regulatory mechanisms that control two ocular lens differentiation pathways
Q91620759	Prognostic classification of endometrial cancer using a molecular approach based on a twelve-gene NGS panel
Q55404843	Prognostic significance of frequent CLDN18-ARHGAP26/6 fusion in gastric signet-ring cell cancer.
Q38660226	Prolonged Mek1/2 suppression impairs the developmental potential of embryonic stem cells
Q30457030	Promiscuous RNA binding by Polycomb repressive complex 2.
Q27675215	Promoter-Specific Transcription Inhibition in Staphylococcus aureus by a Phage Protein
Q38796863	Promoter-Targeted Histone Acetylation of Chromatinized Parvoviral Genome Is Essential for the Progress of Infection
Q56928080	Promotes Invasion through a 3'-Hairpin Structure and Associates with Prognosis in Glioblastoma
Q46166089	Pronounced strain-specific chemosensory receptor gene expression in the mouse vomeronasal organ
Q57802938	Prophage-driven genomic structural changes promote Bartonella vertical evolution
Q45999303	Prospective feasibility trial for genomics-informed treatment in recurrent and progressive glioblastoma.
Q40594870	Protecting genome integrity during CRISPR immune adaptation
Q35109703	Protective variant associated with alcohol dependence in a Mexican American cohort.
Q28486149	Protein complex interactor analysis and differential activity of KDM3 subfamily members towards H3K9 methylation
Q90341634	Protein kinase B controls Mycobacterium tuberculosis growth via phosphorylation of the transcriptional regulator Lsr2 at threonine 112
Q40922968	Proteins that bind regulatory regions identified by histone modification chromatin immunoprecipitations and mass spectrometry.
Q96305534	Proteogenomic Characterization of Ovarian HGSC Implicates Mitotic Kinases, Replication Stress in Observed Chromosomal Instability
Q46262908	Proteogenomic Re-Annotation of Coccidioides posadasii Strain Silveira
Q38670152	Proteogenomics from a bioinformatics angle: A growing field.
Q38743141	Proteogenomics: Key Driver for Clinical Discovery and Personalized Medicine
Q57181405	ProteomeGenerator: A framework for comprehensive proteomics based on de novo transcriptome assembly and high-accuracy peptide mass spectral matching
Q66311259	Proteomic and transcriptomic experiments reveal an essential role of RNA degradosome complexes in shaping the transcriptome of Mycobacterium tuberculosis.
Q92153633	Protocols, Methods, and Tools for Genome-Wide Association Studies (GWAS) of Dental Traits
Q40412706	Protracted Regional Dissemination of GIM-1-Producing Serratia marcescens in Western Germany
Q39266196	Proximal and distal regulation of the HYAL1 gene cluster by the estrogen receptor α in breast cancer cells.
Q93381591	Proximity-CLIP provides a snapshot of protein-occupied RNA elements in subcellular compartments
Q28506146	Pruning of the adipocyte peroxisome proliferator-activated receptor γ cistrome by hematopoietic master regulator PU.1
Q35002752	Pseudogene-derived small interference RNAs regulate gene expression in African Trypanosoma brucei
Q52669141	Pseudomonas aeruginosa MutL promotes large chromosomal deletions through non-homologous end joining to prevent bacteriophage predation.
Q60458126	Pugh et al. reply
Q47227310	Purification of nanogram-range immunoprecipitated DNA in ChIP-seq application.
Q36333062	Putative alternative polyadenylation (APA) events in the early interaction of Salmonella enterica Typhimurium and human host cells
Q36183056	Q-nexus: a comprehensive and efficient analysis pipeline designed for ChIP-nexus
Q90726048	QTL Mapping Combined With Comparative Analyses Identified Candidate Genes for Reduced Shattering in Setaria italica
Q64073823	QTL analysis reveals genomic variants linked to high-temperature fermentation performance in the industrial yeast
Q91635254	QTL-seq reveals a major root-knot nematode resistance locus on chromosome 11 in rice (Oryza sativa L.).
Q30981345	QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments
Q38834954	Quality control material for the detection of somatic mutations in fixed clinical specimens by next-generation sequencing
Q36639581	Quantifying prion disease penetrance using large population control cohorts
Q37727998	Quantitative Analysis of the KSHV Transcriptome Following Primary Infection of Blood and Lymphatic Endothelial Cells
Q90354921	Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) Deletions
Q90098516	Quantitative MNase-seq accurately maps nucleosome occupancy levels
Q60952467	Quantitative RNAseq analysis of Ugandan KS tumors reveals KSHV gene expression dominated by transcription from the LTd downstream latency promoter
Q35668891	Quantitative and qualitative analysis of small RNAs in human endothelial cells and exosomes provides insights into localized RNA processing, degradation and sorting
Q35510689	Quantitative trait loci mapping and transcriptome analysis reveal candidate genes regulating the response to ozone in Arabidopsis thaliana
Q38865552	Quasispecies evolution of the prototypical genotype 1 porcine reproductive and respiratory syndrome virus early during in vivo infection is rapid and tissue specific.
Q36358400	QueryOR: a comprehensive web platform for genetic variant analysis and prioritization
Q90664437	R1 retrotransposons in the nucleolar organizers of Drosophila melanogaster are transcribed by RNA polymerase I upon heat shock
Q91714241	RAS and TP53 can predict survival in adults with T-cell lymphoblastic leukemia treated with hyper-CVAD
Q28272822	RBPJ mutations identified in two families affected by Adams-Oliver syndrome
Q39724925	RECOT: a tool for the coordinate transformation of next-generation sequencing reads for comparative genomics and transcriptomics
Q35941335	RED: A Java-MySQL Software for Identifying and Visualizing RNA Editing Sites Using Rule-Based and Statistical Filters
Q35957395	REPdenovo: Inferring De Novo Repeat Motifs from Short Sequence Reads
Q96136661	RIC-seq for global in situ profiling of RNA-RNA spatial interactions
Q36783636	RIPSeeker: a statistical package for identifying protein-associated transcripts from RIP-seq experiments
Q30460141	RNA Duplex Map in Living Cells Reveals Higher-Order Transcriptome Structure
Q90114572	RNA Interactions Are Essential for CTCF-Mediated Genome Organization
Q90426893	RNA Polymerase II CTD phosphatase Rtr1 fine-tunes transcription termination
Q38791523	RNA Polymerase III Subunit POLR3G Regulates Specific Subsets of PolyA+ and SmallRNA Transcriptomes and Splicing in Human Pluripotent Stem Cells
Q42094679	RNA Sequencing Identifies New RNase III Cleavage Sites in Escherichia coli and Reveals Increased Regulation of mRNA.
Q46313094	RNA editing in bacteria recodes multiple proteins and regulates an evolutionarily conserved toxin-antitoxin system.
Q55034887	RNA m6A methylation participates in regulation of postnatal development of the mouse cerebellum.
Q102152446	RNA nucleation by MSL2 induces selective X chromosome compartmentalization
Q100464437	RNA oxidation in chromatin modification and DNA-damage response following exposure to formaldehyde
Q35970109	RNA regulatory elements and polyadenylation in plants
Q30275185	RNA sequencing analysis of the developing chicken retina
Q64915125	RNA sequencing dataset characterizing transcriptomic responses to dietary changes in Caenorhabditis elegans.
Q43087316	RNA sequencing reveals a unique fusion of the lysine (K)-specific methyltransferase 2A and smooth muscle myosin heavy chain 11 in myelodysplastic syndrome and acute myeloid leukemia
Q48222115	RNA sequencing reveals candidate genes and polymorphisms related to sperm DNA integrity in testis tissue from boars.
Q29114114	RNA sequencing uncovers antisense RNAs and novel small RNAs in Streptococcus pyogenes
Q24613446	RNA sequencing: platform selection, experimental design, and data interpretation
Q58803757	RNA variant identification discrepancy among splice-aware alignment algorithms
Q37272415	RNA-DNA differences in human mitochondria restore ancestral form of 16S ribosomal RNA
Q38306181	RNA-Seq analysis identifies aberrant RNA splicing of TRIP12 in acute myeloid leukemia patients at remission
Q35657467	RNA-Seq analysis identifies genes associated with differential reproductive success under drought-stress in accessions of wild barley Hordeum spontaneum
Q35232930	RNA-Seq analysis reveals a six-gene SoxR regulon in Streptomyces coelicolor
Q34563170	RNA-Seq for enrichment and analysis of IRF5 transcript expression in SLE.
Q37620016	RNA-Seq of Guar (Cyamopsis tetragonoloba, L. Taub.) Leaves: De novo Transcriptome Assembly, Functional Annotation and Development of Genomic Resources
Q35969277	RNA-Seq reveals different mRNA abundance of transporters and their alternative transcript isoforms during liver development
Q35014723	RNA-Seq reveals differential gene expression in Staphylococcus aureus with single-nucleotide resolution
Q31168175	RNA-Sequencing data supports the existence of novel VEGFA splicing events but not of VEGFAxxxb isoforms
Q36331974	RNA-directed DNA methylation enforces boundaries between heterochromatin and euchromatin in the maize genome
Q37534033	RNA-seq analysis of host and viral gene expression highlights interaction between varicella zoster virus and keratinocyte differentiation.
Q45721922	RNA-seq and Tn-seq reveal fitness determinants of vancomycin-resistant Enterococcus faecium during growth in human serum
Q33726183	RNA-seq detects pharmacological inhibition of Epstein-Barr virus late transcription during spontaneous reactivation
Q34781501	RNA-seq in the tetraploid Xenopus laevis enables genome-wide insight in a classic developmental biology model organism
Q36690973	RNA-seq of human reference RNA samples using a thermostable group II intron reverse transcriptase.
Q60053956	RNA-seq of spinal cord from nerve-injured rats after spinal cord stimulation
Q35557833	RNA-seq profiling of small numbers of Drosophila neurons
Q91480456	RNA-seq: Basic Bioinformatics Analysis
Q64091356	RNA-sequencing in ophthalmology research: considerations for experimental design and analysis
Q35860638	RNASEQR--a streamlined and accurate RNA-seq sequence analysis program
Q35576306	RNASeqBrowser: a genome browser for simultaneous visualization of raw strand specific RNAseq reads and UCSC genome browser custom tracks
Q90428483	RNAi pathways repress reprogramming of C. elegans germ cells during heat stress
Q39174680	RNAi-mediated endogene silencing in strawberry fruit: detection of primary and secondary siRNAs by deep sequencing.
Q33735198	RNAseq Reveals Complex Response of Campylobacter jejuni to Ovine Bile and In vivo Gallbladder Environment
Q57788029	RNAsik: A Pipeline for complete and reproducible RNA-seq analysis that runs anywhere with speed and ease
Q92628483	RNA‑seq analyses of antibiotic resistance mechanisms in Serratia marcescens
Q39286785	RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population
Q99234097	RNF40 exerts stage-dependent functions in differentiating osteoblasts and is essential for bone cell crosstalk
Q34817306	RNF43 is frequently mutated in colorectal and endometrial cancers
Q38704619	RNase III nucleases from diverse kingdoms serve as antiviral effectors
Q36791586	RNase J depletion leads to massive changes in mRNA abundance in Helicobacter pylori.
Q57022984	RNase Y-mediated regulation of the streptococcal pyrogenic exotoxin B
Q62666886	ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm
Q101216896	Rampant loss of social traits during domestication of a Bacillus subtilis natural isolate
Q39553559	Rapid Evolution of Genomic Imprinting in Two Species of the Brassicaceae
Q50254380	Rapid Gene Isolation Using MutChromSeq.
Q51037836	Rapid Molecular Genetic Diagnosis with Next-Generation Sequencing in 46,XY Disorders of Sex Development Cases: Efficiency and Cost Assessment.
Q63246429	Rapid Sequencing of Multiple RNA Viruses in Their Native Form
Q90474323	Rapid construction of a whole-genome mutant library by combining haploid stem cells and inducible self-inactivating PiggyBac transposon
Q53189714	Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies.
Q46262604	Rapid evolutionary divergence of diploid and allotetraploid Gossypium mitochondrial genomes
Q46465136	Rapid identification of causal mutations in tomato EMS populations via mapping-by-sequencing.
Q35674956	Rapid mapping of insertional mutations to probe cell wall regulation in Cryptococcus neoformans.
Q38680107	Rapid recovery gene downregulation during excess-light stress and recovery in Arabidopsis.
Q35101229	Rapid reprogramming of epigenetic and transcriptional profiles in mammalian culture systems
Q92404644	Rapid response of stage IV colorectal cancer with APC/TP53/KRAS mutations to FOLFIRI and Bevacizumab combination chemotherapy: a case report of use of liquid biopsy
Q45845784	Rapid turnover of effectors in grass powdery mildew (Blumeria graminis).
Q34820081	Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units
Q35993050	Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours
Q37334870	Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort
Q36228563	Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration
Q61794392	Rare but Recurrent ROS1 Fusions Resulting From Chromosome 6q22 Microdeletions are Targetable Oncogenes in Glioma
Q41518202	Rare frequency of gene variation and survival analysis in thymic epithelial tumors
Q33570108	Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma
Q35462598	Rare variants in MYD88, IRAK4 and IKBKG and susceptibility to invasive pneumococcal disease: a population-based case-control study
Q46273166	Rat embryonic stem cells produce fertile offspring through tetraploid complementation
Q90389207	Rationally engineered Staphylococcus aureus Cas9 nucleases with high genome-wide specificity
Q61448015	Rbf Activates the Myogenic Transcriptional Program to Promote Skeletal Muscle Differentiation
Q37522718	Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutation
Q28272354	Re-evaluation of G-quadruplex propensity with G4Hunter
Q30561080	ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data
Q89621472	Read Mapping and Transcript Assembly: A Scalable and High-Throughput Workflow for the Processing and Analysis of Ribonucleic Acid Sequencing Data
Q39331856	ReadXplorer 2-detailed read mapping analysis and visualization from one single source.
Q30575805	Reanalysis of RNA-sequencing data reveals several additional fusion genes with multiple isoforms
Q91740198	Recapitulation-like developmental transitions of chromatin accessibility in vertebrates
Q90641525	Recent advances in the detection of base modifications using the Nanopore sequencer
Q48344768	Recessive distal motor neuropathy with pyramidal signs in an Omani kindred: underlying novel mutation in the SIGMAR1 gene.
Q34040436	Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.
Q37510181	Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos
Q46572109	Reconstructing the evolutionary history of gypsy retrotransposons in the Périgord black truffle (Tuber melanosporum Vittad.).
Q36543140	Reconstruction of the insulin-like signalling pathway of Haemonchus contortus
Q92740797	Recurrent KRAS mutations identified in papillary renal neoplasm with reverse polarity-a comparative study with papillary renal cell carcinoma
Q46298833	Recurrent Reverse Evolution Maintains Polymorphism after Strong Bottlenecks in Commensal Gut Bacteria.
Q27851991	Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
Q27852975	Recurrent SMARCA4 mutations in small cell carcinoma of the ovary.
Q37274872	Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma
Q50918699	Recurrent and functional regulatory mutations in breast cancer.
Q41054780	Recurrent background mutations in WHI2 impair proteostasis and degradation of misfolded cytosolic proteins in Saccharomyces cerevisiae
Q30276545	Recurrent cis-SAGe chimeric RNA, D2HGDH-GAL3ST2, in prostate cancer
Q50657891	Recurrent genetic defects in classical Hodgkin lymphoma cell lines.
Q96431758	Recurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancer
Q36886180	Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth
Q34473466	Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing
Q90612765	Recurrent non-coding U1-snRNA mutations drive cryptic splicing in Shh medulloblastoma
Q46269827	Recurrent pre-existing and acquired DNA copy number alterations, including focal TERT gains, in neuroblastoma central nervous system metastases
Q33858203	Recurrent read-through fusion transcripts in breast cancer
Q93043299	Redefining the Etiologic Landscape of Cerebellar Malformations
Q35698700	Redeployment of Myc and E2f1-3 drives Rb-deficient cell cycles
Q35189423	Reduced Representation Libraries from DNA Pools Analysed with Next Generation Semiconductor Based-Sequencing to Identify SNPs in Extreme and Divergent Pigs for Back Fat Thickness
Q90568014	Reduced Virulence of an Introduced Forest Pathogen over 50 Years
Q36414237	Reduced infectivity of adenovirus type 5 particles and degradation of entering viral genomes associated with incomplete processing of the preterminal protein
Q38697838	Reducing GWAS Complexity
Q92933271	Reducing the structure bias of RNA-Seq reveals a large number of non-annotated non-coding RNA
Q30592670	Reference-free SNP discovery for the Eurasian beaver from restriction site-associated DNA paired-end data
Q52659858	Refined ab initio gene predictions of Heterorhabditis bacteriophora using RNA-seq.
Q37254115	Refinement of the androgen response element based on ChIP-Seq in androgen-insensitive and androgen-responsive prostate cancer cell lines.
Q38262646	Regenerant Arabidopsis lineages display a distinct genome-wide spectrum of mutations conferring variant phenotypes
Q36826668	Region of difference 4 in alpine Mycobacterium caprae isolates indicates three variants
Q35959575	Regulation of Budding Yeast CENP-A levels Prevents Misincorporation at Promoter Nucleosomes and Transcriptional Defects.
Q42168169	Regulation of DNA demethylation by the XPC DNA repair complex in somatic and pluripotent stem cells
Q36559646	Regulation of Hepatic Drug-Metabolizing Enzymes in Germ-Free Mice by Conventionalization and Probiotics
Q38287444	Regulation of Peripheral Myelination through Transcriptional Buffering of Egr2 by an Antisense Long Non-coding RNA.
Q42135241	Regulation of alternative polyadenylation by Nkx2-5 and Xrn2 during mouse heart development
Q34582328	Regulation of angiopoietin-like protein 4 production during and after exercise.
Q37628541	Regulation of hepatic microRNA expression by hepatocyte nuclear factor 4 alpha
Q41726404	Regulation of p53 and Rb links the alternative NF-κB pathway to EZH2 expression and cell senescence.
Q30608522	Regulation of synaptic transmission at the Caenorhabditis elegans M4 neuromuscular junction by an antagonistic relationship between two calcium channels.
Q36068080	Regulation of the BMP Signaling-Responsive Transcriptional Network in the Drosophila Embryo
Q41349840	Regulation of the glucocorticoid receptor via a BET-dependent enhancer drives antiandrogen resistance in prostate cancer.
Q92679684	Regulatory factor X5 promotes hepatocellular carcinoma progression by transactivating tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta and suppressing apoptosis
Q28535431	Regulatory phosphorylation of Ikaros by Bruton's tyrosine kinase
Q41911065	Relapse-specific mutations in NT5C2 in childhood acute lymphoblastic leukemia
Q64107619	Relative Mutation Rates in Nucleomorph-Bearing Algae
Q41747137	Relative contributions of the structural and catalytic roles of Rrp6 in exosomal degradation of individual mRNAs
Q47108079	Relevance of iPSC-derived human PGC-like cells at the surface of embryoid bodies to prechemotaxis migrating PGCs.
Q38622361	Reliable Detection of Herpes Simplex Virus Sequence Variation by High-Throughput Resequencing.
Q55510434	Remapping of the belted phenotype in cattle on BTA3 identifies a multiplication event as the candidate causal mutation.
Q33989254	Remodeling of the methylation landscape in breast cancer metastasis.
Q56961547	Reorganization of chromosomal interactions in the 2q37-deletion syndrome
Q92030536	RepViz: a replicate-driven R tool for visualizing genomic regions
Q100395415	Repeat expansions confer WRN dependence in microsatellite-unstable cancers
Q58705343	Repeated inversions within a pannier intron drive diversification of intraspecific colour patterns of ladybird beetles
Q22122001	Repetitive DNA and next-generation sequencing: computational challenges and solutions
Q52862108	Replication fork progression is paused in two large chromosomal zones flanking the DNA replication origin in Escherichia coli.
Q89575670	Replicational Dilution of H3K27me3 in Mammalian Cells and the Role of Poised Promoters
Q59810740	Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
Q50928301	Replisome-mediated translesion synthesis by a cellular replicase.
Q34050798	Reporting tumor molecular heterogeneity in histopathological diagnosis
Q33751768	Repression of chimeric transcripts emanating from endogenous retrotransposons by a sequence-specific transcription factor
Q33900874	Requirement for flap endonuclease 1 (FEN1) to maintain genomic stability and transcriptional gene silencing in Arabidopsis
Q57462404	Requirements for Neurogenin2 during mouse postnatal retinal neurogenesis
Q34295514	Research resource: RNA-Seq reveals unique features of the pancreatic β-cell transcriptome.
Q48272510	Residual disease detection using targeted parallel sequencing predicts relapse in cytogenetically normal acute myeloid leukemia.
Q51144717	Resilience of small intestinal beneficial bacteria to the toxicity of soybean oil fatty acids.
Q90261023	Resistance Evolution against Phage Combinations Depends on the Timing and Order of Exposure
Q51004850	Resistance to RET-Inhibition in RET-Rearranged NSCLC Is Mediated By Reactivation of RAS/MAPK Signaling.
Q58199146	Resistance to the Plant Defensin NaD1 Features Modifications to the Cell Wall and Osmo-Regulation Pathways of Yeast
Q51102156	Responsiveness of Brca1 and Trp53 Deficiency-Induced Mammary Preneoplasia to Selective Estrogen Modulators versus an Aromatase Inhibitor in Mus musculus.
Q47959883	Retrograde inhibition by a specific subset of interpeduncular α5 nicotinic neurons regulates nicotine preference.
Q93366339	Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndrome
Q46477691	Retrotransposon-Mediated Aluminum Tolerance through Enhanced Expression of the Citrate Transporter OsFRDL4.
Q64111855	Revealing the dominant long noncoding RNAs responding to the infection with Colletotrichum gloeosporioides in Hevea brasiliensis
Q41433576	Rho-associated kinase is a therapeutic target in neuroblastoma
Q51739609	Rht18 Semi-Dwarfism in Wheat is Due to Increased Expression of GA 2-oxidaseA9 and Lower GA Content.
Q36040254	Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency
Q60302530	Ribonuclease H1-targeted R-loops in surface antigen gene expression sites can direct trypanosome immune evasion
Q49544465	Ribosome Profiling in Maize.
Q54998021	Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development.
Q41845109	Ribosome profiling reveals post-transcriptional buffering of divergent gene expression in yeast.
Q48158685	Rice nucleosome patterns undergo remodeling coincident with stress-induced gene expression.
Q36306292	Risk for molecular contamination of tissue samples evaluated for targeted anti-cancer therapy
Q61814878	Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
Q92881276	Robust Suppression of Lipopolysaccharide Deficiency in Acinetobacter baumannii by Growth in Minimal Medium
Q35881001	Robust gene expression and mutation analyses of RNA-sequencing of formalin-fixed diagnostic tumor samples.
Q55109103	Robustness encoded across essential and accessory replicons of the ecologically versatile bacterium Sinorhizobium meliloti.
Q36461293	Role of molecular testing in the multidisciplinary diagnostic approach of ichthyosis.
Q34497855	Role of recurrent hypoxia-ischemia in preterm white matter injury severity
Q60958057	Role of the pre-initiation complex in Mediator recruitment and dynamics
Q36359347	Rsx is a metatherian RNA with Xist-like properties in X-chromosome inactivation
Q42775550	Rule-based integration of RNA-Seq analyses tools for identification of novel transcripts
Q96135726	Runaway multi-allelic copy number variation at the α-defensin locus in African and Asian populations
Q43438056	SAMSCOPE: an OpenGL-based real-time interactive scale-free SAM viewer
Q100745322	SARS-CoV-2 Disrupts Splicing, Translation, and Protein Trafficking to Suppress Host Defenses
Q110175413	SARS-CoV-2 expresses a microRNA-like small RNA able to selectively repress host genes
Q42400918	SC3-seq: a method for highly parallel and quantitative measurement of single-cell gene expression.
Q37724020	SERS detection of the biomarker hydrogen cyanide from Pseudomonas aeruginosa cultures isolated from cystic fibrosis patients
Q34093678	SF3B1 and other novel cancer genes in chronic lymphocytic leukemia
Q104064528	SIRT3, a metabolic target linked to ataxia-telangiectasia mutated (ATM) gene deficiency in diffuse large B-cell lymphoma
Q59087455	SIRT6 deficiency results in developmental retardation in cynomolgus monkeys
Q92493623	SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus
Q47323767	SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency
Q51819259	SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
Q38755115	SMAC Mimetic Birinapant plus Radiation Eradicates Human Head and Neck Cancers with Genomic Amplifications of Cell Death Genes FADD and BIRC2.
Q37285370	SMAR1 binds to T(C/G) repeat and inhibits tumor progression by regulating miR-371-373 cluster.
Q61800369	SMARCA4 loss is synthetic lethal with CDK4/6 inhibition in non-small cell lung cancer
Q64063071	SMARCAD1 ATPase activity is required to silence endogenous retroviruses in embryonic stem cells
Q60930247	SMARTcleaner: identify and clean off-target signals in SMART ChIP-seq analysis
Q34263872	SMIM1 underlies the Vel blood group and influences red blood cell traits
Q42282822	SNHG16 is regulated by the Wnt pathway in colorectal cancer and affects genes involved in lipid metabolism
Q41666724	SNP rs7770370 in HLA-DPB1 loci as a major genetic determinant of response to booster hepatitis B vaccination: results of a genome-wide association study
Q36206289	SOX15 governs transcription in human stratified epithelia and a subset of esophageal adenocarcinomas
Q50062529	SOX2 regulates common and specific stem cell features in the CNS and endoderm derived organs.
Q64254902	SQuIRE reveals locus-specific regulation of interspersed repeat expression
Q30586217	SRAdb: query and use public next-generation sequencing data from within R.
Q30670690	STAR: an integrated solution to management and visualization of sequencing data
Q47701637	STAT5-mediated chromatin interactions in superenhancers activate IL-2 highly inducible genes: Functional dissection of the Il2ra gene locus.
Q30822375	SUMOylated NKAP is essential for chromosome alignment by anchoring CENP-E to kinetochores
Q41941328	SUMOylation regulates the chromatin occupancy and anti-proliferative gene programs of glucocorticoid receptor
Q37018778	SV-STAT accurately detects structural variation via alignment to reference-based assemblies.
Q34188360	SVA: software for annotating and visualizing sequenced human genomes
Q38883033	SVPV: a structural variant prediction viewer for paired-end sequencing datasets
Q42696101	SVmine improves structural variation detection by integrative mining of predictions from multiple algorithms
Q65002016	SWI/SNF and RSC cooperate to reposition and evict promoter nucleosomes at highly expressed genes in yeast.
Q90228015	SWI/SNF remains localized to chromatin in the presence of SCHLAP1
Q49114614	Salmonella Gallinarum field isolates from laying hens are related to the vaccine strain SG9R.
Q42126101	Savant Genome Browser 2: visualization and analysis for population-scale genomics
Q58791714	Schizosaccharomyces pombe Pol II transcription elongation factor ELL functions as part of a rudimentary super elongation complex
Q57185099	Screening for regulatory variants in 460kb encompassing the CFTR locus in cystic fibrosis patients
Q59353526	Screening for viral nucleic acids in vestibular schwannoma
Q30578213	Scribl: an HTML5 Canvas-based graphics library for visualizing genomic data over the web
Q30910406	Scrimer: designing primers from transcriptome data.
Q91995004	Seasonal Stability and Dynamics of DNA Methylation in Plants in a Natural Environment
Q92817976	Second-Hit, Postzygotic PMVK and MVD Mutations in Linear Porokeratosis
Q41691425	Secondary Somatic Mutations Restoring RAD51C and RAD51D Associated with Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma
Q36298683	Segmental duplications and evolutionary acquisition of UV damage response in the SPATA31 gene family of primates and humans
Q36346318	Segmentum: a tool for copy number analysis of cancer genomes
Q36111981	Selecting Hypomethylated Genomic Regions Using MRE-Seq.
Q35924591	Selection against recombinant hybrids maintains reproductive isolation in hybridizing Populus species despite F1 fertility and recurrent gene flow
Q48255098	Selection for a Zinc-Finger Protein Contributes to Seed Oil Increase during Soybean Domestication.
Q89935051	Selective Enrichment of A-to-I Edited Transcripts from Cellular RNA Using Endonuclease V
Q37630264	Selective Whole-Genome Amplification Is a Robust Method That Enables Scalable Whole-Genome Sequencing of Plasmodium vivax from Unprocessed Clinical Samples.
Q33167243	Semiconductor Whole Exome Sequencing for the Identification of Genetic Variants in Colombian Patients Clinically Diagnosed with Long QT Syndrome
Q93101149	Sensitive Detection and Analysis of Neoantigen-Specific T Cell Populations from Tumors and Blood
Q48113220	Sensitive detection of mitochondrial DNA variants for analysis of mitochondrial DNA-enriched extracts from frozen tumor tissue
Q90371597	Sensitive detection of pre-integration intermediates of long terminal repeat retrotransposons in crop plants
Q93096440	Sensitivity, advantages, limitations, and clinical utility of targeted next-generation sequencing panels for the diagnosis of selected lysosomal storage disorders
Q96953990	Seq-ing answers: Current data integration approaches to uncover mechanisms of transcriptional regulation
Q33946035	SeqGene: a comprehensive software solution for mining exome- and transcriptome- sequencing data
Q31094439	SeqPurge: highly-sensitive adapter trimming for paired-end NGS data
Q31044437	Seqinspector: position-based navigation through the ChIP-seq data landscape to identify gene expression regulators
Q36944530	Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk
Q39048994	Sequence and functional characterization of hypoxia-inducible factors, HIF1α, HIF2αa, and HIF3α, from the estuarine fish, Fundulus heteroclitus
Q37599715	Sequence of Reston Virus Isolate AZ-1435, an Ebolavirus Isolate Obtained during the 1989-1990 Reston Virus Epizootic in the United States.
Q47262872	Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing
Q37159937	Sequencing of 279 cancer genes in ampullary carcinoma reveals trends relating to histologic subtypes and frequent amplification and overexpression of ERBB2 (HER2)
Q34145763	Sequencing of pooled DNA samples (Pool-Seq) uncovers complex dynamics of transposable element insertions in Drosophila melanogaster
Q35554760	Sequencing small genomic targets with high efficiency and extreme accuracy.
Q64076450	Sequencing the Obligate Intracellular Rhabdochlamydia helvetica within Its Tick Host Ixodes ricinus to Investigate Their Symbiotic Relationship
Q39083031	Sequential analysis of 18 genes in polycythemia vera and essential thrombocythemia reveals an association between mutational status and clinical outcome.
Q90724422	Serial mutational tracking in surgically resected locally advanced colorectal cancer with neoadjuvant chemotherapy
Q50254642	Serial translocation by means of circular intermediates underlies colour sidedness in cattle.
Q28117414	Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation
Q90235789	Severe Acute Respiratory Syndrome Coronavirus 2 from Patient with 2019 Novel Coronavirus Disease, United States
Q64260570	Sex differences in gene regulation in the dorsal root ganglion after nerve injury
Q38603799	Sex-based differences in myocardial gene expression in recently deceased organ donors with no prior cardiovascular disease.
Q28315290	Shedding light on cell compartmentation in the candidate phylum Poribacteria by high resolution visualisation and transcriptional profiling
Q38809600	Short DNA Hairpins Compromise Recombinant Adeno-Associated Virus Genome Homogeneity.
Q98735749	Short and Long-Read Sequencing Survey of the Dynamic Transcriptomes of African Swine Fever Virus and the Host Cells
Q95617230	Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions
Q106272052	Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions
Q41906242	Shugoshin biases chromosomes for biorientation through condensin recruitment to the pericentromere
Q92971130	Signal Integration of IFN-I and IFN-II With TLR4 Involves Sequential Recruitment of STAT1-Complexes and NFκB to Enhance Pro-inflammatory Transcription
Q64103892	Signal peptide peptidase activity connects the unfolded protein response to plant defense suppression by Ustilago maydis
Q54956145	Signatures of host specialization and a recent transposable element burst in the dynamic one-speed genome of the fungal barley powdery mildew pathogen.
Q64946672	Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2.
Q47831063	Silencing of retrotransposons by SETDB1 inhibits the interferon response in acute myeloid leukemia.
Q98288806	Similar Seed Composition Phenotypes Are Observed From CRISPR-Generated In-Frame and Knockout Alleles of a Soybean KASI Ortholog
Q93161863	Similarities and differences in patterns of germline mutation between mice and humans
Q46128590	Similarity between soybean and Arabidopsis seed methylomes and loss of non-CG methylation does not affect seed development
Q41381031	Simple Expression Domains Are Regulated by Discrete CRMs During Drosophila Oogenesis
Q55223250	Simultaneous identification of clinically relevant single nucleotide variants, copy number alterations and gene fusions in solid tumors by targeted next-generation sequencing.
Q92492876	Simultaneous precise editing of multiple genes in human cells
Q33701387	Simultaneous processing and degradation of mitochondrial RNAs revealed by circularized RNA sequencing
Q30411399	Simultaneous profiling of 194 distinct receptor transcripts in human cells
Q35063762	Simultaneous transcriptional profiling of bacteria and their host cells
Q93151313	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
Q35832334	Single Base-Resolution Methylome of the Dizygotic Sheep
Q57294154	Single Cell and Open Chromatin Analysis Reveals Molecular Origin of Epidermal Cells of the Skin
Q88368782	Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patients
Q56774692	Single Nucleotide Variants in A Family of Monozygotic Twins Discordant for the Phenotype Congenital Megaureter: A Genomic Analysis
Q40106239	Single TRAM domain RNA-binding proteins in Archaea: functional insight from Ctr3 from the Antarctic methanogen Methanococcoides burtonii
Q36857904	Single molecule real-time sequencing of Xanthomonas oryzae genomes reveals a dynamic structure and complex TAL (transcription activator-like) effector gene relationships.
Q34757795	Single nucleotide polymorphism typing with massively parallel sequencing for human identification
Q47722248	Single nucleotide polymorphisms in genes encoding penicillin-binding proteins in β-lactamase-negative ampicillin-resistant Haemophilus influenzae in Japan.
Q90379938	Single sample sequencing (S3EQ) of epigenome and transcriptome in nucleus accumbens
Q97421905	Single-cell ATAC sequencing analysis: From data preprocessing to hypothesis generation
Q36333706	Single-cell RNA-seq reveals changes in cell cycle and differentiation programs upon aging of hematopoietic stem cells
Q92938684	Single-cell alternative splicing analysis reveals dominance of single transcript variant
Q35607837	Single-cell analysis of lung adenocarcinoma cell lines reveals diverse expression patterns of individual cells invoked by a molecular target drug treatment
Q37510607	Single-cell analysis of mixed-lineage states leading to a binary cell fate choice.
Q28388773	Single-cell transcriptogenomics reveals transcriptional exclusion of ENU-mutated alleles
Q99595210	Single-gene imaging links genome topology, promoter-enhancer communication and transcription control
Q57465832	Single-molecule DNA-mapping and whole-genome sequencing of individual cells
Q35863236	Single-molecule real-time transcript sequencing facilitates common wheat genome annotation and grain transcriptome research
Q34799278	Single-tube, highly parallel mutation enrichment in cancer gene panels by use of temperature-tolerant COLD-PCR.
Q41455914	Site-specific genome editing in Plasmodium falciparum using engineered zinc-finger nucleases
Q50621435	Sixteen additional enhancers associated with the chicken Sox2 locus outside the central 50-kb region.
Q90480132	Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion
Q42353182	Slit-Robo GTPase-Activating Protein 2 as a metastasis suppressor in osteosarcoma.
Q64883492	Smad4 deficiency impairs chondrocyte hypertrophy via the Runx2 transcription factor in mouse skeletal development.
Q47686883	Small RNA profiling in Chlamydomonas: insights into chloroplast RNA metabolism
Q46246769	Small RNA repertoires and their intraspecies variation in Aggregatibacter actinomycetemcomitans
Q50034195	Small RNAs of Haloferax mediterranei: Identification and Potential Involvement in Nitrogen Metabolism.
Q59137913	Small non-coding RNA expression in mouse nephrogenic mesenchymal progenitors
Q64254907	Small nucleolar RNAs controlling rRNA processing in Trypanosoma brucei
Q93129281	Small-Molecule Targeting of Oncogenic FTO Demethylase in Acute Myeloid Leukemia
Q90724394	Sno-derived RNAs are prevalent molecular markers of cancer immunity
Q35613225	Software solutions for the livestock genomics SNP array revolution.
Q31159453	Software tools for visualizing Hi-C data
Q34549516	Somatic ERCC2 mutations correlate with cisplatin sensitivity in muscle-invasive urothelial carcinoma
Q36233887	Somatic Mutation Patterns in Hemizygous Genomic Regions Unveil Purifying Selection during Tumor Evolution
Q55353370	Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types.
Q37060418	Somatic SETBP1 mutations in myeloid malignancies
Q37179645	Somatic Variants in the Human Lens Epithelium: A Preliminary Assessment
Q37100131	Somatic alterations contributing to metastasis of a castration-resistant prostate cancer
Q36850521	Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes
Q35837219	Somatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case.
Q89987468	Somatic mRNA Analysis of BRCA1 Splice Variants Provides a Direct Theranostic Impact on PARP Inhibitors
Q93046091	Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy
Q38886065	Somatic mutations reveal asymmetric cellular dynamics in the early human embryo
Q92463012	Somatic mutations substantially increase the per-generation mutation rate in the conifer Picea sitchensis
Q35310932	Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient
Q35046527	Somatic point mutation calling in low cellularity tumors.
Q33839390	Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing
Q41369944	Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly.
Q64970633	Sources of erroneous sequences and artifact chimeric reads in next generation sequencing of genomic DNA from formalin-fixed paraffin-embedded samples.
Q34089148	Sox5 and c-Maf cooperatively induce Th17 cell differentiation via RORγt induction as downstream targets of Stat3.
Q37095297	Sox9 and Sox8 protect the adult testis from male-to-female genetic reprogramming and complete degeneration.
Q92652633	Spatial Distance Correlates With Genetic Distance in Diffuse Glioma
Q49832163	Spatial Tissue Proteomics Quantifies Inter- and Intratumor Heterogeneity in Hepatocellular Carcinoma (HCC).
Q28649475	Spatial and temporal heterogeneity in high-grade serous ovarian cancer: a phylogenetic analysis
Q90027737	Spatial and temporal inhibition of FGFR2b ligands reveals continuous requirements and novel targets in mouse inner ear morphogenesis
Q41436943	Spatial genomic heterogeneity in multiple myeloma revealed by multi-region sequencing
Q95941505	Spatial inter-centromeric interactions facilitated the emergence of evolutionary new centromeres
Q36167042	Spatio-temporal mutation profiles of case-matched colorectal carcinomas and their metastases reveal unique de novo mutations in metachronous lung metastases by targeted next generation sequencing.
Q36256686	Spatio-temporal regulation of circular RNA expression during porcine embryonic brain development
Q35948476	Speciation in Cloudless Sulphurs Gleaned from Complete Genomes
Q48020178	Specific Inhibition of the Bifunctional Farnesyl/Geranylgeranyl Diphosphate Synthase in Malaria Parasites via a New Small-Molecule Binding Site
Q36212908	Spectrum of somatic mitochondrial mutations in five cancers
Q100378834	Sperm-specific COX6B2 enhances oxidative phosphorylation, proliferation, and survival in human lung adenocarcinoma
Q89720871	Sphingosine 1-Phosphate Receptor Signaling Establishes AP-1 Gradients to Allow for Retinal Endothelial Cell Specialization
Q89855423	Sphingosine 1-phosphate-regulated transcriptomes in heterogenous arterial and lymphatic endothelium of the aorta
Q92240377	Spinal cord stimulation prevents paclitaxel-induced mechanical and cold hypersensitivity and modulates spinal gene expression in rats
Q64943976	Splice-Break: exploiting an RNA-seq splice junction algorithm to discover mitochondrial DNA deletion breakpoints and analyses of psychiatric disorders.
Q31032615	SpliceJumper: a classification-based approach for calling splicing junctions from RNA-seq data
Q42774216	Spliced synthetic genes as internal controls in RNA sequencing experiments
Q88571202	Spliceosome Profiling Visualizes Operations of a Dynamic RNP at Nucleotide Resolution
Q41169795	Spontaneous dominant mutations in chlamydomonas highlight ongoing evolution by gene diversification
Q91838671	Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Q30861981	SraTailor: graphical user interface software for processing and visualizing ChIP-seq data.
Q37417986	Stable Caenorhabditis elegans chromatin domains separate broadly expressed and developmentally regulated genes
Q34312075	Stable intronic sequence RNA (sisRNA), a new class of noncoding RNA from the oocyte nucleus of Xenopus tropicalis.
Q35878585	Standardizing chromatin research: a simple and universal method for ChIP-seq.
Q36072723	Stochastic alternative splicing is prevalent in mungbean (Vigna radiata).
Q59357572	Strand-Specific Dual RNA Sequencing of Bronchial Epithelial Cells Infected with Influenza A/H3N2 Viruses Reveals Splicing of Gene Segment 6 and Novel Host-Virus Interactions
Q35824626	Strand-Specific RNA-Seq Analyses of Fruiting Body Development in Coprinopsis cinerea
Q35047843	Strategic approaches to unraveling genetic causes of cardiovascular diseases
Q57465697	Streptococcal Lancefield polysaccharides are critical cell wall determinants for human Group IIA secreted phospholipase A2 to exert its bactericidal effects
Q49838620	Streptomyces coelicolor strains lacking polyprenol phosphate mannose synthase and protein O-mannosyl transferase are hyper-susceptible to multiple antibiotics.
Q34548457	Streptomyces exploration is triggered by fungal interactions and volatile signals
Q37181935	Stress and corticosteroids regulate rat hippocampal mitochondrial DNA gene expression via the glucocorticoid receptor.
Q36745030	Strictly co-isogenic C57BL/6J-Prnp-/- mice: A rigorous resource for prion science
Q55515962	Striking circadian neuron diversity and cycling of Drosophila alternative splicing.
Q39740957	Strong mutational bias toward deletions in the Drosophila melanogaster genome is compensated by selection
Q58763989	Structural Variants and Selective Sweep Foci Contribute to Insecticide Resistance in the Genetic Reference Panel
Q33921205	Structural and functional differences in the long non-coding RNA hotair in mouse and human
Q90465976	Structural basis for distinct roles of SMAD2 and SMAD3 in FOXH1 pioneer-directed TGF-β signaling
Q47131186	Structural basis for genome wide recognition of 5-bp GC motifs by SMAD transcription factors
Q35754667	Structural evidence for Scc4-dependent localization of cohesin loading
Q34501830	Structural genomic changes underlie alternative reproductive strategies in the ruff (Philomachus pugnax).
Q103836656	Structural modularity of the XIST ribonucleoprotein complex
Q31043037	Structural variation detection using next-generation sequencing data: A comparative technical review.
Q35847837	Structural variation on the human Y chromosome from population-scale resequencing
Q40161265	Structure of O-Antigen and Hybrid Biosynthetic Locus in Burkholderia cenocepacia Clonal Variants Recovered from a Cystic Fibrosis Patient.
Q97522781	Structure-based design of gRNA for Cas13
Q99561634	Studies of rice Hd1 haplotypes worldwide reveal adaptation of flowering time to different environments
Q90275876	Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma
Q64027552	Study of mitotic chromatin supports a model of bookmarking by histone modifications and reveals nucleosome deposition patterns
Q61443084	Study of the whole genome, methylome and transcriptome of Cordyceps militaris
Q34615175	Sturgeon conservation genomics: SNP discovery and validation using RAD sequencing
Q31135205	Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate.
Q35854307	Substantial DNA methylation differences between two major neuronal subtypes in human brain
Q37720623	Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency
Q41228615	Succinate dehydrogenase deficiency in a PDGFRA mutated GIST.
Q64230557	Sumoylation of DNA-bound transcription factor Sko1 prevents its association with nontarget promoters
Q59125265	Sumoylation of RORγt regulates T17 differentiation and thymocyte development
Q41175754	Sumoylation of Rap1 mediates the recruitment of TFIID to promote transcription of ribosomal protein genes
Q37649083	Sun exposure causes somatic second-hit mutations and angiofibroma development in tuberous sclerosis complex
Q64062867	Sunbeam: an extensible pipeline for analyzing metagenomic sequencing experiments
Q47135291	Super enhancer associated RAI14 is a new potential biomarker in lung adenocarcinoma
Q92534099	Super-Enhancer-Associated Hub Genes In Chronic Myeloid Leukemia Identified Using Weighted Gene Co-Expression Network Analysis
Q47750108	Super-enhancers define a proliferative PGC-1α-expressing melanoma subgroup sensitive to BET inhibition.
Q38640368	SuperTranscripts: a data driven reference for analysis and visualisation of transcriptomes
Q96946557	Suppression of proteolipid protein rescues Pelizaeus-Merzbacher disease
Q91933279	SureSelect targeted enrichment, a new cost effective method for the whole genome sequencing of Candidatus Liberibacter asiaticus
Q35998897	Survey of cryptic unstable transcripts in yeast
Q51830452	Surveying the lipogenesis landscape in Yarrowia lipolytica through understanding the function of a Mga2p regulatory protein mutant.
Q98184101	Symmetric neural progenitor divisions require chromatin-mediated homologous recombination DNA repair by Ino80
Q89738625	Synthetic CRISPR/Cas9 reagents facilitate genome editing and homology directed repair
Q58799724	Synthetic microbe communities provide internal reference standards for metagenome sequencing and analysis
Q30707670	SysBioCube: A Data Warehouse and Integrative Data Analysis Platform Facilitating Systems Biology Studies of Disorders of Military Relevance
Q52607316	Systematic Analysis of Splice-Site-Creating Mutations in Cancer.
Q36888921	Systematic Characterization of Long Noncoding RNAs Reveals the Contrasting Coordination of Cis- and Trans-Molecular Regulation in Human Fetal and Adult Hearts.
Q91936605	Systematic allelic analysis defines the interplay of key pathways in X chromosome inactivation
Q37396432	Systematic comparison of monoclonal versus polyclonal antibodies for mapping histone modifications by ChIP-seq
Q37214774	Systematic discovery of complex insertions and deletions in human cancers.
Q33591245	Systematic functional perturbations uncover a prognostic genetic network driving human breast cancer
Q37164922	Systematic interrogation of 3q26 identifies TLOC1 and SKIL as cancer drivers.
Q33709312	Systematic mapping of functional enhancer-promoter connections with CRISPR interference
Q42777362	Systems Biology Analyses in Chicken: Workflow for Transcriptome and ChIP-Seq Analyses Using the Chicken Skin Paradigm
Q55021404	T Cell Receptor Alpha Chain Genes in the Teleost Ballan Wrasse (Labrus bergylta) Are Subjected to Somatic Hypermutation.
Q92153654	TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish
Q91688131	TAGOOS: genome-wide supervised learning of non-coding loci associated to complex phenotypes
Q34322512	TAPDANCE: an automated tool to identify and annotate transposon insertion CISs and associations between CISs from next generation sequence data
Q100428012	TASOR is a pseudo-PARP that directs HUSH complex assembly and epigenetic transposon control
Q47755605	TBX4 is involved in the super-enhancer-driven transcriptional programs underlying features specific to lung fibroblasts.
Q28118952	TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function
Q92285876	TEG001 Insert Integrity from Vector Producer Cells until Medicinal Product
Q48152733	TGF-β uses a novel mode of receptor activation to phosphorylate SMAD1/5 and induce epithelial-to-mesenchymal transition
Q38830217	TIAM1 variants improve clinical outcome in neuroblastoma
Q90299366	TIE: A Method to Electroporate Long DNA Templates into Preimplantation Embryos for CRISPR-Cas9 Gene Editing
Q92430876	TIN2 Functions with TPP1/POT1 To Stimulate Telomerase Processivity
Q57335035	TIN2 functions with TPP1/POT1 to stimulate telomerase processivity
Q31109634	TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data.
Q55177617	TP53 and OSBPL10 alterations in diffuse large B-cell lymphoma: prognostic markers identified via exome analysis of cases with extreme prognosis.
Q37326100	TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing
Q35606212	TP53 mutation characteristics in therapy-related myelodysplastic syndromes and acute myeloid leukemia is similar to de novo diseases
Q39439144	TP53 mutations emerge with HDM2 inhibitor SAR405838 treatment in de-differentiated liposarcoma
Q35961836	TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer
Q36345993	TRE5-A retrotransposition profiling reveals putative RNA polymerase III transcription complex binding sites on the Dictyostelium extrachromosomal rDNA element.
Q28732805	TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data
Q42510422	TRPC1 is a differential regulator of hypoxia-mediated events and Akt signalling in PTEN-deficient breast cancer cells
Q38429142	TSS-Seq analysis of low pH-induced gene expression in intercalated cells in the renal collecting duct
Q89526901	Targetable ERBB2 mutations identified in neurofibroma/schwannoma hybrid nerve sheath tumors
Q57482125	Targeted DamID reveals differential binding of mammalian pluripotency factors
Q41064767	Targeted Disruption of TCF12 Reveals HEB as Essential in Human Mesodermal Specification and Hematopoiesis
Q38283644	Targeted NGS meets expert clinical characterization: Efficient diagnosis of spastic paraplegia type 11.
Q37694797	Targeted NGS, array-CGH, and patient-derived tumor xenografts for precision medicine in advanced breast cancer: a single-center prospective study
Q35937517	Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material
Q35906993	Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility
Q61452046	Targeted Next-Generation Sequencing of , and Genes in Patients with Endometrial Carcinoma under 50 Years of Age
Q36093648	Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2
Q43179664	Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells
Q37186761	Targeted capture massively parallel sequencing analysis of LCIS and invasive lobular cancer: Repertoire of somatic genetic alterations and clonal relationships
Q90602286	Targeted fusion analysis can aid in the classification and treatment of pediatric glioma, ependymoma, and glioneuronal tumors
Q64388953	Targeted genome fragmentation with CRISPR/Cas9 enables fast and efficient enrichment of small genomic regions and ultra-accurate sequencing with low DNA input (CRISPR-DS)
Q57797078	Targeted genotyping of variable number tandem repeats with adVNTR
Q47100599	Targeted inhibition of STAT/TET1 axis as a therapeutic strategy for acute myeloid leukemia.
Q64058813	Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neoplasms
Q60507082	Targeted next-generation sequencing and fine linkage disequilibrium mapping reveals association of PNPLA3 and PARVB with the severity of nonalcoholic fatty liver disease
Q39328851	Targeted next-generation sequencing for TP53, RAS, BRAF, ALK and NF1 mutations in anaplastic thyroid cancer.
Q38634870	Targeted next-generation sequencing of commonly mutated genes in esophageal adenocarcinoma patients with long-term survival
Q94563184	Targeted reprogramming of H3K27me3 resets epigenetic memory in plant paternal chromatin
Q34323456	Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations.
Q36635602	Targeted resequencing reveals ALK fusions in non-small cell lung carcinomas detected by FISH, immunohistochemistry, and real-time RT-PCR: a comparison of four methods
Q90602942	Targeted sequencing identifies novel variants in common and rare MODY genes
Q96952509	Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants
Q64118643	Targeted, High-Resolution RNA Sequencing of Non-coding Genomic Regions Associated With Neuropsychiatric Functions
Q91892527	Targeting REGNASE-1 programs long-lived effector T cells for cancer therapy
Q35842471	Targeting chromatin binding regulation of constitutively active AR variants to overcome prostate cancer resistance to endocrine-based therapies
Q64951709	Targeting enhancer switching overcomes non-genetic drug resistance in acute myeloid leukaemia.
Q55438295	Targeting the IGF1R Pathway in Breast Cancer Using Antisense lncRNA-Mediated Promoter cis Competition.
Q59329522	Targets and genomic constraints of ectopic Dnmt3b expression
Q90455761	Tbx2a modulates switching of RH2 and LWS opsin gene expression
Q50114214	Technical adequacy of bisulfite sequencing and pyrosequencing for detection of mitochondrial DNA methylation: Sources and avoidance of false-positive detection.
Q89884669	Technological advances and computational approaches for alternative splicing analysis in single cells
Q28066706	Technological considerations for genome-guided diagnosis and management of cancer
Q37587816	Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene
Q97556089	Telomere-to-telomere assembly of a complete human X chromosome
Q90123559	Temperature preference can bias parental genome retention during hybrid evolution
Q36240637	Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
Q89603312	Template plasmid integration in germline genome-edited cattle
Q36462320	Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in DICER1 syndrome: a unique variant of the two-hit tumor suppression model
Q41662098	Temporal regulation of epithelium formation mediated by FoxA, MKLP1, MgcRacGAP, and PAR-6.
Q46267199	Temporal variation in brain transcriptome is associated with the expression of female mimicry as a sequential male alternative reproductive tactic in fish.
Q61449402	Ten-Eleven Translocation Proteins Modulate the Response to Environmental Stress in Mice
Q37618285	Testis-specific transcriptional regulators selectively occupy BORIS-bound CTCF target regions in mouse male germ cells
Q89767252	Thalidomide Inhibits Human iPSC Mesendoderm Differentiation by Modulating CRBN-dependent Degradation of SALL4
Q90062528	Thanatogenomic Investigation of the Hydroxymethylome and Mitochondrial Genome of Cadaveric Cardiomyocytes: Proposal for a Proof-of-Concept Study
Q46302412	The 5' region of Xist RNA has the potential to associate with chromatin through the A-repeat
Q41911201	The APSES transcription factor Efg1 is a global regulator that controls morphogenesis and biofilm formation in Candida parapsilosis.
Q38677249	The Antisense Transcriptome and the Human Brain.
Q47854281	The Arabidopsis DNA Methylome Is Stable under Transgenerational Drought Stress.
Q28600842	The Arabidopsis thaliana mobilome and its impact at the species level
Q47810281	The Arcuate Estrogen-Regulated Transcriptome: Estrogen Response Element-Dependent and -Independent Signaling of ERα in Female Mice
Q90247028	The BRCA2 mutation status shapes the immune phenotype of prostate cancer
Q33693698	The Biomphalaria glabrata DNA methylation machinery displays spatial tissue expression, is differentially active in distinct snail populations and is modulated by interactions with Schistosoma mansoni
Q34490455	The Brucella abortus virulence regulator, LovhK, is a sensor kinase in the general stress response signalling pathway
Q34522844	The CRISPR-associated DNA-cleaving enzyme Cpf1 also processes precursor CRISPR RNA.
Q51041496	The CRISPR/Cas system can be used as nuclease for in planta gene targeting and as paired nickases for directed mutagenesis in Arabidopsis resulting in heritable progeny.
Q35897778	The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C1935 and CYP2C192 Alleles
Q35066321	The Cancer Genome Atlas (TCGA): an immeasurable source of knowledge
Q116166948	The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
Q34516725	The ChIP-seq-defined networks of Bcl-3 gene binding support its required role in skeletal muscle atrophy
Q57753911	The Chromatin Remodelers PKL and PIE1 Act in an Epigenetic Pathway That Determines H3K27me3 Homeostasis in Arabidopsis
Q42363612	The Chromatin Remodeling Component Arid1a Is a Suppressor of Spontaneous Mammary Tumors in Mice
Q31122609	The Complete Plastid Genome Sequence of Madagascar Periwinkle Catharanthus roseus (L.) G. Don: Plastid Genome Evolution, Molecular Marker Identification, and Phylogenetic Implications in Asterids
Q41729977	The Conserved RNA Binding Cyclophilin, Rct1, Regulates Small RNA Biogenesis and Splicing Independent of Heterochromatin Assembly
Q41676526	The Conserved Spore Coat Protein SpoVM Is Largely Dispensable in Clostridium difficile Spore Formation
Q57752878	The DEAD-box protein Dbp2p is linked to non-coding RNAs, the helicase Sen1p, and R-loops
Q58097668	The DNA binding landscape of the maize AUXIN RESPONSE FACTOR family
Q28585866	The DNA methyltransferase DNMT3C protects male germ cells from transposon activity
Q37631872	The Dictyostelium discoideum RNA-dependent RNA polymerase RrpC silences the centromeric retrotransposon DIRS-1 post-transcriptionally and is required for the spreading of RNA silencing signals
Q35126655	The Drosophila melanogaster phospholipid flippase dATP8B is required for odorant receptor function
Q47566135	The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis.
Q52682480	The End of a 60-year Riddle: Identification and Genomic Characterization of an Iridovirus, the Causative Agent of White Fat Cell Disease in Zooplankton.
Q36195236	The Epstein-Barr Virus Immunoevasins BCRF1 and BPLF1 Are Expressed by a Mechanism Independent of the Canonical Late Pre-initiation Complex
Q41929920	The Epstein-Barr virus miR-BHRF1 microRNAs regulate viral gene expression in cis.
Q64975748	The Functional Change and Deletion of FLC Homologs Contribute to the Evolution of Rapid Flowering in Boechera stricta.
Q49464678	The GAN Exonuclease or the Flap Endonuclease Fen1 and RNase HII Are Necessary for Viability of Thermococcus kodakarensis.
Q91963622	The Genetic Basis of Scale-Loss Phenotype in the Rapid Radiation of Takifugu Fishes
Q38358515	The Genome 10K Project: a way forward
Q58725917	The Genome of the Human Pathogen Is Shaped by Mutation and Cryptic Sexual Recombination
Q41739963	The Genomic Landscape of Male Breast Cancers
Q64882616	The Genomic and Immune Landscapes of Lethal Metastatic Breast Cancer.
Q56979625	The Gulf Familial Hypercholesterolemia Registry (Gulf FH): Design, Rationale and Preliminary Results
Q50568919	The H3K27 demethylase Utx regulates somatic and germ cell epigenetic reprogramming.
Q101216854	The HUSH complex is a gatekeeper of type I interferon through epigenetic regulation of LINE-1s
Q51055717	The Hippo Pathway Maintains the Equatorial Division Plane in the Ciliate Tetrahymena.
Q36324942	The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies
Q49243720	The IAP family member BRUCE regulates autophagosome-lysosome fusion.
Q28395556	The IL-4/STAT6 signaling axis establishes a conserved microRNA signature in human and mouse macrophages regulating cell survival via miR-342-3p
Q36958976	The ISW1 and CHD1 ATP-dependent chromatin remodelers compete to set nucleosome spacing in vivo
Q41930014	The Immature Fiber Mutant Phenotype of Cotton (Gossypium hirsutum) Is Linked to a 22-bp Frame-Shift Deletion in a Mitochondria Targeted Pentatricopeptide Repeat Gene.
Q34540922	The Impact of Endurance Training on Human Skeletal Muscle Memory, Global Isoform Expression and Novel Transcripts
Q35610506	The Intraperitoneal Transcriptome of the Opportunistic Pathogen Enterococcus faecalis in Mice
Q92666241	The Landscape of Phenotypic and Transcriptional Responses to Ciprofloxacin in Acinetobacter baumannii: Acquired Resistance Alleles Modulate Drug-Induced SOS Response and Prophage Replication
Q39045655	The Lipocalin LPR-1 Cooperates with LIN-3/EGF Signaling To Maintain Narrow Tube Integrity in Caenorhabditis elegans
Q36216749	The Long Noncoding RNA Transcriptome of Dictyostelium discoideum Development
Q90085329	The Loz1 transcription factor from Schizosaccharomyces pombe binds to Loz1 response elements and represses gene expression when zinc is in excess
Q28647488	The Mitochondrial Genomes of a Myxozoan Genus Kudoa Are Extremely Divergent in Metazoa
Q27932238	The Modifier of Transcription 1 (Mot1) ATPase and Spt16 Histone Chaperone Co-regulate Transcription through Preinitiation Complex Assembly and Nucleosome Organization
Q35774021	The Mosaic Mutants of Cucumber: A Method to Produce Knock-Downs of Mitochondrial Transcripts
Q64056599	The NRF2 transcriptional target NQO1 has low mRNA levels in TP53-mutated endometrial carcinomas
Q38723756	The New Immortalized Uroepithelial Cell Line HBLAK Contains Defined Genetic Aberrations Typical of Early Stage Urothelial Tumors.
Q36898306	The Nuclear Receptor Rev-erbα Regulates Adipose Tissue-specific FGF21 Signaling.
Q30757620	The PSI-U1 snRNP interaction regulates male mating behavior in Drosophila
Q91661378	The Per-1 Short Isoform Inhibits de novo HIV-1 Transcription in Resting CD4+ T-cells
Q38371542	The Proteomics Standards Initiative: Fifteen Years of Progress and Future Work.
Q58751705	The Pseudomonas aeruginosa Complement of Lactate Dehydrogenases Enables Use of d- and l-Lactate and Metabolic Cross-Feeding
Q47329879	The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability
Q89789461	The R-loop Atlas of Arabidopsis Development and Responses to Environmental Stimuli
Q48165811	The R-loop is a common chromatin feature of the Arabidopsis genome.
Q63352011	The RNA Complement of Outer Membrane Vesicles From Serovar Typhimurium Under Distinct Culture Conditions
Q97069756	The RNA quality control pathway nonsense-mediated mRNA decay targets cellular and viral RNAs to restrict KSHV
Q90385766	The RNA-binding protein ILF3 binds to transposable element sequences in SINEUP lncRNAs
Q36051478	The Regulation of rRNA Gene Transcription during Directed Differentiation of Human Embryonic Stem Cells
Q42710675	The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
Q67200930	The Role of mA/m-RNA Methylation in Stress Response Regulation
Q42317152	The Saccharomyces cerevisiae Cdk8 Mediator Represses AQY1 Transcription by Inhibiting Set1p-Dependent Histone Methylation.
Q30491879	The Sequences of 1,504 Mutants in the Model Rice Variety Kitaake Facilitate Rapid Functional Genomic Studies
Q64106084	The Stat3-Fam3a axis promotes muscle stem cell myogenic lineage progression by inducing mitochondrial respiration
Q46264534	The Substrates of Nonsense-Mediated mRNA Decay in Caenorhabditis elegans
Q38892531	The Suf Iron-Sulfur Cluster Biosynthetic System Is Essential in Staphylococcus aureus, and Decreased Suf Function Results in Global Metabolic Defects and Reduced Survival in Human Neutrophils.
Q34293334	The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement
Q47135795	The Terpene Synthase Gene Family of Carrot (Daucus carota L.): Identification of QTLs and Candidate Genes Associated with Terpenoid Volatile Compounds
Q55362090	The Transcription Factor NFATc1 Supports the Rejection of Heterotopic Heart Allografts.
Q40403691	The Transcriptional Regulator CpsY Is Important for Innate Immune Evasion in Streptococcus pyogenes
Q55070232	The Transcriptional Regulator TFB-RF1 Activates Transcription of a Putative ABC Transporter in Pyrococcus furiosus.
Q83227667	The Tudor SND1 protein is an mA RNA reader essential for replication of Kaposi's sarcoma-associated herpesvirus
Q28273417	The UCSC genome browser and associated tools
Q60922622	The USTC co-opts an ancient machinery to drive piRNA transcription in
Q61226710	The UTX Tumor Suppressor Directly Senses Oxygen to Control Chromatin and Cell Fate
Q30560932	The Wasp System: an open source environment for managing and analyzing genomic data.
Q50026513	The ZBED6-IGF2 axis has a major effect on growth of skeletal muscle and internal organs in placental mammals.
Q42557721	The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform
Q107377255	The architecture of the SARS-CoV-2 RNA genome inside virion
Q42565688	The atm-1 gene is required for genome stability in Caenorhabditis elegans
Q91895462	The bread wheat epigenomic map reveals distinct chromatin architectural and evolutionary features of functional genetic elements
Q51417803	The bromodomain-containing protein Ibd1 links multiple chromatin-related protein complexes to highly expressed genes in Tetrahymena thermophila.
Q28266682	The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data
Q52346019	The characteristics of ctDNA reveal the high complexity in matching the corresponding tumor tissues.
Q28959147	The chromatin remodeler DDM1 promotes hybrid vigor by regulating salicylic acid metabolism
Q42375711	The common oncogenomic program of NOTCH1 and NOTCH3 signaling in T-cell acute lymphoblastic leukemia
Q46265993	The complete chloroplast genome of Primulina and two novel strategies for development of high polymorphic loci for population genetic and phylogenetic studies
Q54593059	The complete mitochondrial genome of Corydoras nattereri (Callichthyidae: Corydoradinae)
Q35763824	The complete mitochondrial genome of Papilio glaucus and its phylogenetic implications
Q35735793	The complete mitochondrial genome sequence of the green microalga Lobosphaera (Parietochloris) incisa reveals a new type of palindromic repetitive repeat
Q39004486	The complete nucleotide sequence and genomic characterization of tropical soda apple mosaic virus
Q90731028	The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material
Q92802021	The conserved transcriptional regulator CdnL is required for metabolic homeostasis and morphogenesis in Caulobacter
Q33991747	The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population
Q107341981	The coronavirus proofreading exoribonuclease mediates extensive viral recombination
Q92094548	The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease
Q33892323	The distinct biological implications of Asxl1 mutation and its roles in leukemogenesis revealed by a knock-in mouse model
Q92515742	The diversity, evolution and ecology of Salmonella in venomous snakes
Q47575452	The dynamic evolution of Drosophila innubila Nudivirus
Q38399916	The dynamics of diverse segmental amplifications in populations of Saccharomyces cerevisiae adapting to strong selection
Q36036383	The effect of acute and long-term physical activity on extracellular matrix and serglycin in human skeletal muscle
Q37408471	The epidemic of extended-spectrum-β-lactamase-producing Escherichia coli ST131 is driven by a single highly pathogenic subclone, H30-Rx
Q35248451	The evolution of drug resistance in clinical isolates of Candida albicans
Q38395382	The evolutionary history of Afrocanarian blue tits inferred from genomewide SNPs
Q47102996	The evolutionary landscape of chronic lymphocytic leukemia treated with ibrutinib targeted therapy.
Q46569048	The evolutionary origin of CIPK16: A gene involved in enhanced salt tolerance.
Q53374376	The exercise-regulated myokine chitinase-3-like protein 1 stimulates human myocyte proliferation.
Q31108080	The exon quantification pipeline (EQP): a comprehensive approach to the quantification of gene, exon and junction expression from RNA-seq data
Q28545135	The exosome component Rrp6 is required for RNA polymerase II termination at specific targets of the Nrd1-Nab3 pathway
Q38950591	The fire ant social chromosome supergene variant Sb shows low diversity but high divergence from SB
Q91841455	The first clawed lobster virus Homarus gammarus nudivirus (HgNV n. sp.) expands the diversity of the Nudiviridae
Q28235419	The first steps of adaptation of Escherichia coli to the gut are dominated by soft sweeps
Q35642077	The fitness consequences of aneuploidy are driven by condition-dependent gene effects
Q107162400	The folate antagonist methotrexate diminishes replication of the coronavirus SARS-CoV-2 and enhances the antiviral efficacy of remdesivir in cell culture models
Q36728081	The fruRBA Operon Is Necessary for Group A Streptococcal Growth in Fructose and for Resistance to Neutrophil Killing during Growth in Whole Human Blood
Q34430420	The fungal pathogen Moniliophthora perniciosa has genes similar to plant PR-1 that are highly expressed during its interaction with cacao
Q96229566	The genetic basis of sex determination in grapes
Q37697911	The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models
Q36929803	The genetic landscape of high-risk neuroblastoma
Q30453771	The genetic landscape of mutations in Burkitt lymphoma
Q89947923	The genetics of situs inversus without primary ciliary dyskinesia
Q37678930	The genome of Leishmania adleri from a mammalian host highlights chromosome fission in Sauroleishmania
Q38647819	The genome of the cotton bacterial blight pathogen Xanthomonas citri pv. malvacearum strain MSCT1.
Q40435497	The genome sequence and insights into the immunogenetics of the bananaquit (Passeriformes: Coereba flaveola).
Q34430957	The genome sequence of African rice (Oryza glaberrima) and evidence for independent domestication.
Q36098131	The genome-scale DNA-binding profile of BarR, a β-alanine responsive transcription factor in the archaeon Sulfolobus acidocaldarius
Q42131091	The genomic signature of breast cancer prevention
Q57753804	The helicase Ded1p controls use of near-cognate translation initiation codons in 5' UTRs
Q47095631	The hepatic circadian clock fine-tunes the lipogenic response to feeding through RORα/γ.
Q35929073	The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.
Q35004518	The highly prolific phenotype of Lacaune sheep is associated with an ectopic expression of the B4GALNT2 gene within the ovary
Q93039172	The histone chaperone CAF-1 cooperates with the DNA methyltransferases to maintain Cd4 silencing in cytotoxic T cells
Q47371049	The histone code reader Spin1 controls skeletal muscle development.
Q41338406	The histone deacetylase SIRT6 controls embryonic stem cell fate via TET-mediated production of 5-hydroxymethylcytosine.
Q33728316	The histone demethylase KDM3A regulates the transcriptional program of the androgen receptor in prostate cancer cells
Q67226106	The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape
Q92179712	The histone methyltransferase EZH2 primes the early differentiation of follicular helper T cells during acute viral infection
Q94567739	The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double strand break repair
Q35973139	The impact and origin of copy number variations in the Oryza species
Q47724817	The increased expression of follicle-stimulating hormone leads to a decrease of fecundity in transgenic Large White female pigs.
Q42698634	The integration site of the APP transgene in the J20 mouse model of Alzheimer's disease
Q92761409	The internal loops in the lower stem of primary microRNA transcripts facilitate single cleavage of human Microprocessor
Q37061192	The landscape of RNA polymerase II transcription initiation in C. elegans reveals promoter and enhancer architectures
Q34437602	The landscape of kinase fusions in cancer
Q53089292	The landscape of somatic mutations in Down syndrome-related myeloid disorders.
Q39338325	The liver transcriptome of suckermouth armoured catfish (Pterygoplichthys anisitsi, Loricariidae): Identification of expansions in defensome gene families
Q92217658	The lncRNA SLNCR Recruits the Androgen Receptor to EGR1-Bound Genes in Melanoma and Inhibits Expression of Tumor Suppressor p21
Q28687241	The lysine specific demethylase-1 (LSD1/KDM1A) regulates VEGF-A expression in prostate cancer
Q30448141	The maize methylome influences mRNA splice sites and reveals widespread paramutation-like switches guided by small RNA.
Q36639417	The major histocompatibility complex in Old World camelids and low polymorphism of its class II genes
Q45062538	The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain.
Q38680908	The miR-23a~27a~24-2 microRNA cluster buffers transcription and signaling pathways during hematopoiesis
Q64114365	The molecular mechanism of dsRNA processing by a bacterial Dicer
Q92596654	The multi-allelic APRR2 gene is associated with fruit pigment accumulation in melon and watermelon
Q37003447	The mutational landscape of adenoid cystic carcinoma
Q29614654	The mutational landscape of head and neck squamous cell carcinoma
Q57174763	The mutational landscape of recurrent versus nonrecurrent human papillomavirus-related oropharyngeal cancer
Q38892311	The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia
Q94474181	The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice
Q40337066	The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression
Q55100603	The novel 19q13 KRAB zinc-finger tumour suppressor ZNF382 is frequently methylated in oesophageal squamous cell carcinoma and antagonises Wnt/β-catenin signalling.
Q92937229	The nucleosome acidic patch directly interacts with subunits of the Paf1 and FACT complexes and controls chromatin architecture in vivo
Q41105157	The oncocytic subtype is genetically distinct from other pancreatic intraductal papillary mucinous neoplasm subtypes.
Q35149661	The p53 transcriptional pathway is preserved in ATMmutated and NOTCH1mutated chronic lymphocytic leukemias.
Q90265606	The pH Signaling Transcription Factor PAC-3 Regulates Metabolic and Developmental Processes in Pathogenic Fungi
Q55080767	The parthenocarpic gene Pat-k is generated by a natural mutation of SlAGL6 affecting fruit development in tomato (Solanum lycopersicum L.).
Q92534361	The pause-initiation limit restricts transcription activation in human cells
Q34735951	The performance of BRCA1 immunohistochemistry for detecting germline, somatic, and epigenetic BRCA1 loss in high-grade serous ovarian cancer
Q57785565	The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature
Q92611367	The phosphatase PAC1 acts as a T cell suppressor and attenuates host antitumor immunity
Q30835101	The piggyBac transposon-derived genes TPB1 and TPB6 mediate essential transposon-like excision during the developmental rearrangement of key genes in Tetrahymena thermophila
Q38650850	The practical use of genome sequencing data in the management of a feline colony pedigree
Q47554097	The proBAM and proBed standard formats: enabling a seamless integration of genomics and proteomics data
Q36213630	The psoriasis-associated deletion of late cornified envelope genes LCE3B and LCE3C has been maintained under balancing selection since Human Denisovan divergence.
Q92832264	The regulatory landscape of a core maize domestication module controlling bud dormancy and growth repression
Q21128789	The rise and fall of the Phytophthora infestans lineage that triggered the Irish potato famine
Q98303537	The role of exome sequencing in newborn screening for inborn errors of metabolism
Q39095773	The role of the poly(A) tract in the replication and virulence of tick-borne encephalitis virus
Q41482499	The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation.
Q48464435	The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome.
Q37736297	The soybean GmSNAP18 gene underlies two types of resistance to soybean cyst nematode
Q37595312	The systematic analysis of coding and long non-coding RNAs in the sub-chronic and chronic stages of spinal cord injury.
Q99412509	The tRNA pseudouridine synthase TruB1 regulates the maturation of let-7 miRNA
Q47345032	The target landscape of clinical kinase drugs
Q96222254	The testis protein ZNF165 is a SMAD3 cofactor that coordinates oncogenic TGFβ signaling in triple-negative breast cancer
Q47670271	The transcription factors GATA2 and microphthalmia-associated transcription factor regulate Hdc gene expression in mast cells and are required for IgE/mast cell-mediated anaphylaxis.
Q36113399	The transcriptional and splicing landscape of intestinal organoids undergoing nutrient starvation or endoplasmic reticulum stress.
Q41858982	The transcriptional regulator Aire binds to and activates super-enhancers
Q39043617	The transcriptional regulatory network mediated by banana (Musa acuminata) dehydration-responsive element binding (MaDREB) transcription factors in fruit ripening
Q34655388	The transcriptome of Leishmania major in the axenic promastigote stage: transcript annotation and relative expression levels by RNA-seq.
Q53819472	The transcriptomic and epigenetic map of vascular quiescence in the continuous lung endothelium.
Q37181385	The two chromosomes of the mitochondrial genome of a sugarcane cultivar: assembly and recombination analysis using long PacBio reads
Q40104482	The two-component response regulator Skn7 belongs to a network of transcription factors regulating morphogenesis in Candida albicans and independently limits morphogenesis-induced ROS accumulation
Q37375173	The ubiquitin ligase CRL2ZYG11 targets cyclin B1 for degradation in a conserved pathway that facilitates mitotic slippage.
Q98564796	The ubiquitin ligase Cullin-1 associates with chromatin and regulates transcription of specific c-MYC target genes
Q61455138	The unfolded protein response and endoplasmic reticulum protein targeting machineries converge on the stress sensor IRE1
Q46553634	The walnut (Juglans regia) genome sequence reveals diversity in genes coding for the biosynthesis of non-structural polyphenols
Q27936820	The yeast Snt2 protein coordinates the transcriptional response to hydrogen peroxide-mediated oxidative stress
Q92072940	Thermal Manipulation During Embryogenesis Impacts H3K4me3 and H3K27me3 Histone Marks in Chicken Hypothalamus
Q46713825	Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.
Q28730091	Three acyltransferases and nitrogen-responsive regulator are implicated in nitrogen starvation-induced triacylglycerol accumulation in Chlamydomonas
Q37371138	Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model
Q48198794	TimeLapse-seq: adding a temporal dimension to RNA sequencing through nucleoside recoding.
Q89600501	Tissue alarmins and adaptive cytokine induce dynamic and distinct transcriptional responses in tissue-resident intraepithelial cytotoxic T lymphocytes
Q37145916	Tissue homogeneity requires inhibition of unequal gene silencing during development
Q35780129	Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2
Q37707477	Tissue-specific pioneer factors associate with androgen receptor cistromes and transcription programs
Q64106864	Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans
Q39031144	Tools and Strategies for Analysis of Genome-Wide and Gene-Specific DNA Methylation Patterns
Q28648128	TopFed: TCGA tailored federated query processing and linking to LOD
Q39528312	Topoisomerase 1(TOP1) gene copy number in stage III colorectal cancer patients and its relation to prognosis
Q34826055	Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers
Q35051525	Towards the integration, annotation and association of historical microarray experiments with RNA-seq
Q35193258	Tracing melioidosis back to the source: using whole-genome sequencing to investigate an outbreak originating from a contaminated domestic water supply
Q28396153	Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Q46156568	Tracking the genome-wide outcomes of a transposable element burst over decades of amplification
Q61798013	Tracking the origin of two genetic components associated with transposable element bursts in domesticated rice
Q28088603	Tracks through the genome to physiological events
Q35890750	Trade-Offs of Escherichia coli Adaptation to an Intracellular Lifestyle in Macrophages
Q34664803	Trancriptional landscape of Aspergillus niger at breaking of conidial dormancy revealed by RNA-sequencing
Q48310098	Transcription Factor Interplay between LEAFY and APETALA1/CAULIFLOWER during Floral Initiation
Q34490684	Transcription factor co-occupied regions in the murine genome constitute T-helper-cell subtype-specific enhancers.
Q90471619	Transcription factor p73 regulates Th1 differentiation
Q50102218	Transcription factor-dependent 'anti-repressive' mammalian enhancers exclude H3K27me3 from extended genomic domains.
Q35121362	Transcription factors GATA4 and HNF4A control distinct aspects of intestinal homeostasis in conjunction with transcription factor CDX2.
Q34767064	Transcription mediated insulation and interference direct gene cluster expression switches
Q103027719	Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence
Q90183024	Transcription-dependent targeting of Hda1C to hyperactive genes mediates H4-specific deacetylation in yeast
Q91972654	Transcription-mediated organization of the replication initiation program across large genes sets common fragile sites genome-wide
Q60047560	Transcriptional Landscape of a Plasmid and Response to Imipenem Exposure in TOP10
Q38626630	Transcriptional Profiling of Midguts Prepared from Trypanosoma/T. congolense-Positive Glossina palpalis palpalis Collected from Two Distinct Cameroonian Foci: Coordinated Signatures of the Midguts' Remodeling As T. congolense-Supportive Niches
Q58093893	Transcriptional Regulation of Lipophorin Receptors Supports Neuronal Adaptation to Chronic Elevations of Activity
Q38289993	Transcriptional Regulator CNOT3 Defines an Aggressive Colorectal Cancer Subtype
Q64104965	Transcriptional Reprogramming of Rice Cells by TALEs
Q35663996	Transcriptional Slippage and RNA Editing Increase the Diversity of Transcripts in Chloroplasts: Insight from Deep Sequencing of Vigna radiata Genome and Transcriptome
Q52630978	Transcriptional and epigenetic adaptation of maize chromosomes in Oat-Maize addition lines.
Q58762072	Transcriptional and epigenomic landscapes of CNS and non-CNS vascular endothelial cells
Q40015985	Transcriptional changes are involved in phenotype switching in Streptococcus equi subspecies equi.
Q27311580	Transcriptional control of an essential ribozyme in Drosophila reveals an ancient evolutionary divide in animals
Q49791507	Transcriptional landscape and regulatory roles of small non-coding RNAs in the oxidative stress response of the haloarchaeon Haloferax volcanii.
Q40414012	Transcriptional programs that control expression of the autoimmune regulator gene Aire
Q37157244	Transcriptional response to stress in the dynamic chromatin environment of cycling and mitotic cells
Q35914865	Transcriptional variation in the malaria parasite Plasmodium falciparum
Q50139431	Transcriptome Analysis of a Bloom-Forming Cyanobacterium Microcystis aeruginosa during Ma-LMM01 Phage Infection.
Q35153549	Transcriptome analyses of adult mouse brain reveal enrichment of lncRNAs in specific brain regions and neuronal populations
Q36637180	Transcriptome analysis of Inbred Long Sleep and Inbred Short Sleep mice
Q35121971	Transcriptome analysis of cyst formation in Rhodospirillum centenum reveals large global changes in expression during cyst development
Q36181263	Transcriptome analysis of the fungal pathogen Fusarium oxysporum f. sp. medicaginis during colonisation of resistant and susceptible Medicago truncatula hosts identifies differential pathogenicity profiles and novel candidate effectors.
Q34640139	Transcriptome analysis of the parasite Encephalitozoon cuniculi: an in-depth examination of pre-mRNA splicing in a reduced eukaryote
Q30010106	Transcriptome analysis using next generation sequencing reveals molecular signatures of diabetic retinopathy and efficacy of candidate drugs
Q58786565	Transcriptome and DNA methylome reveal insights into yield heterosis in the curds of broccoli (Brassica oleracea L var. italic)
Q89634274	Transcriptome and Phytochemical Analysis Reveals the Alteration of Plant Hormones, Characteristic Metabolites, and Related Gene Expression in Tea (Camellia sinensis L.) Leaves During Withering
Q92017297	Transcriptome assembly from long-read RNA-seq alignments with StringTie2
Q34927743	Transcriptome deep-sequencing and clustering of expressed isoforms from Favia corals
Q90076689	Transcriptome divergence during leaf development in two contrasting switchgrass (Panicum virgatum L.) cultivars
Q41846723	Transcriptome mapping of pAR060302, a blaCMY-2-positive broad-host-range IncA/C plasmid
Q34315137	Transcriptome sequencing for SNP discovery across Cucumis melo
Q38625509	Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles
Q34361771	Transcriptome sequencing of Eucalyptus camaldulensis seedlings subjected to water stress reveals functional single nucleotide polymorphisms and genes under selection
Q38823157	Transcriptome sequencing reveals thousands of novel long non-coding RNAs in B cell lymphoma
Q60303735	Transcriptome-wide analysis links the short-term expression of the b isoforms of TIA proteins to protective proteostasis-mediated cell quiescence response
Q90241919	Transcriptome-wide analysis of a baculovirus using nanopore sequencing
Q50906731	Transcriptome-wide analysis of vernalization reveals conserved and species-specific mechanisms in Brachypodium.
Q36466905	Transcriptome-wide high-throughput deep m(6)A-seq reveals unique differential m(6)A methylation patterns between three organs in Arabidopsis thaliana.
Q44809252	Transcriptome-wide identification of RNA binding sites by CLIP-seq
Q36392252	Transcriptome-wide measurement of translation by ribosome profiling
Q48509474	Transcriptome-wide survey of gene expression changes and alternative splicing in Trichophyton rubrum in response to undecanoic acid.
Q55339598	Transcriptome-wide survey of pseudorabies virus using next- and third-generation sequencing platforms.
Q87113993	Transcriptome-wide target profiling of RNA cytosine methyltransferases using the mechanism-based enrichment procedure Aza-IP
Q52684155	Transcriptomes define distinct subgroups of salivary gland adenoid cystic carcinoma with different driver mutations and outcomes.
Q40265975	Transcriptomes of Ralstonia solanacearum during Root Colonization of Solanum commersonii
Q36248921	Transcriptomic Analysis of Laribacter hongkongensis Reveals Adaptive Response Coupled with Temperature
Q37731257	Transcriptomic Complexity of Aspergillus terreus Velvet Gene Family under the Influence of Butyrolactone I.
Q92602894	Transcriptomic Profiling of Adipose Derived Stem Cells Undergoing Osteogenesis by RNA-Seq
Q37692788	Transcriptomic analysis reveals metabolic switches and surface remodeling as key processes for stage transition in Trypanosoma cruzi
Q48036109	Transcriptomic fingerprinting of Pseudomonas putida under alternative physiological regimes
Q36175240	Transcriptomic responses of a simplified soil microcosm to a plant pathogen and its biocontrol agent reveal a complex reaction to harsh habitat
Q59333347	Transcriptomic study of Herpes simplex virus type-1 using full-length sequencing techniques
Q42774947	Transcriptomic variation among six Arabidopsis thaliana accessions identified several novel genes controlling aluminium tolerance
Q37707263	Transcriptomics Indicates Active and Passive Metronidazole Resistance Mechanisms in Three Seminal Giardia Lines.
Q27317035	Transcriptomics of diapause in an isogenic self-fertilizing vertebrate
Q36002097	Transformed Recombinant Enrichment Profiling Rapidly Identifies HMW1 as an Intracellular Invasion Locus in Haemophilus influenza
Q39070391	Transition from Environmental to Partial Genetic Sex Determination in Daphnia through the Evolution of a Female-Determining Incipient W Chromosome.
Q91045962	Translation control of the immune checkpoint in cancer and its therapeutic targeting
Q39037306	Translational control of lipogenic enzymes in the cell cycle of synchronous, growing yeast cells
Q95305867	Translational control of one-carbon metabolism underpins ribosomal protein phenotypes in cell division and longevity
Q36439806	Transmembrane proteins UNC-40/DCC, PTP-3/LAR, and MIG-21 control anterior-posterior neuroblast migration with left-right functional asymmetry in Caenorhabditis elegans
Q57464804	Transparent Danionella translucida as a genetically tractable vertebrate brain model
Q89784443	Transposable elements have contributed human regulatory regions that are activated upon bacterial infection
Q34748732	Transposable elements modulate human RNA abundance and splicing via specific RNA-protein interactions
Q97676622	Transposase assisted tagmentation of RNA/DNA hybrid duplexes
Q92997182	Treatment of a Mouse Model of ALS by In Vivo Base Editing
Q28648484	Trends in IT Innovation to Build a Next Generation Bioinformatics Solution to Manage and Analyse Biological Big Data Produced by NGS Technologies
Q37610130	Trinucleotide Repeat Expansion in the Transcription Factor 4 (TCF4) Gene Leads to Widespread mRNA Splicing Changes in Fuchs' Endothelial Corneal Dystrophy
Q47231120	Trithorax dependent changes in chromatin landscape at enhancer and promoter regions drive female puberty
Q33815791	Trp63 is regulated by STAT5 in mammary tissue and subject to differentiation in cancer.
Q30831010	Truncation and constitutive activation of the androgen receptor by diverse genomic rearrangements in prostate cancer.
Q42379279	Trypanosoma cruzi specific mRNA amplification by in vitro transcription improves parasite transcriptomics in host-parasite RNA mixtures
Q35136473	Tumor evolution and intratumor heterogeneity of an epithelial ovarian cancer investigated using next-generation sequencing
Q55518477	Tumor-Specific Mitochondrial DNA Variants Are Rarely Detected in Cell-Free DNA.
Q102061305	Tumor-derived mutations in postoperative plasma of colorectal cancer with microsatellite instability
Q55339783	TumorNext-Lynch-MMR: a comprehensive next generation sequencing assay for the detection of germline and somatic mutations in genes associated with mismatch repair deficiency and Lynch syndrome.
Q37158331	Twin Mitochondrial Sequence Analysis
Q92432426	Two Y-chromosome-encoded genes determine sex in kiwifruit
Q47903893	Two modes of targeting transposable elements by piRNA pathway in human testis.
Q39638001	Type IV pili promote early biofilm formation by Clostridium difficile
Q83230290	Tyr1 phosphorylation promotes phosphorylation of Ser2 on the C-terminal domain of eukaryotic RNA polymerase II by P-TEFb
Q90836153	U1 snRNP regulates chromatin retention of noncoding RNAs
Q47993320	UBE2O remodels the proteome during terminal erythroid differentiation.
Q57034216	UBN1/2 of HIRA complex is responsible for recognition and deposition of H3.3 at cis-regulatory elements of genes in mouse ES cells
Q52430935	UDiTaS™, a genome editing detection method for indels and genome rearrangements.
Q99579422	UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS libraries
Q50986605	UTX promotes hormonally responsive breast carcinogenesis through feed-forward transcription regulation with estrogen receptor.
Q99726393	UTX/KDM6A suppresses AP-1 and a gliogenesis program during neural differentiation of human pluripotent stem cells
Q47169349	Ubiquitin C-terminal hydrolase isozyme L1 is associated with shelterin complex at interstitial telomeric sites.
Q40991461	Ubiquitously expressed genes participate in cell-specific functions via alternative promoter usage.
Q93079010	Ultra-Mutation in IDH Wild-Type Glioblastomas of Patients Younger than 55 Years is Associated with Defective Mismatch Repair, Microsatellite Instability, and Giant Cell Enrichment
Q58699975	Ultra-Sensitive Mutation Detection and Genome-Wide DNA Copy Number Reconstruction by Error-Corrected Circulating Tumor DNA Sequencing
Q35793506	Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis
Q36189043	Unbiased Interrogation of 3D Genome Topology Using Chromosome Conformation Capture Coupled to High-Throughput Sequencing (4C-Seq).
Q62085463	Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells
Q34388528	Uncovering the genome-wide transcriptional responses of the filamentous fungus Aspergillus niger to lignocellulose using RNA sequencing
Q91792615	Understand the genomic diversity and evolution of fungal pathogen Candida glabrata by genome-wide analysis of genetic variations
Q35960793	Understanding butanol tolerance and assimilation in Pseudomonas putida BIRD-1: an integrated omics approach
Q92420208	Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level
Q57984558	Unexpected Genomic and Phenotypic Diversity of Mycobacterium africanum Lineage 5 Affects Drug Resistance, Protein Secretion, and Immunogenicity
Q97423828	Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach
Q52312700	Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.
Q58769123	Unique Molecular Identifiers reveal a novel sequencing artefact with implications for RNA-Seq based gene expression analysis
Q35236669	Unique features of a Japanese 'Candidatus Liberibacter asiaticus' strain revealed by whole genome sequencing
Q35650948	Unique somatic and malignant expression patterns implicate PIWI-interacting RNAs in cancer-type specific biology
Q28534652	Unique transcriptome patterns of the white and grey matter corroborate structural and functional heterogeneity in the human frontal lobe
Q62490013	Unraveling transformation of follicular lymphoma to diffuse large B-cell lymphoma
Q48172707	Untangling Heteroplasmy, Structure, and Evolution of an Atypical Mitochondrial Genome by PacBio Sequencing
Q41243412	Uracil Accumulation and Mutagenesis Dominated by Cytosine Deamination in CpG Dinucleotides in Mice Lacking UNG and SMUG1.
Q35913236	Use of De Novo Transcriptome Libraries to Characterize a Novel Oleaginous Marine Chlorella Species during the Accumulation of Triacylglycerols
Q35806939	Use of illumina deep sequencing technology to differentiate hepatitis C virus variants
Q30808420	Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing Data
Q34782823	Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
Q36164665	Using diverse U.S. beef cattle genomes to identify missense mutations in EPAS1, a gene associated with pulmonary hypertension.
Q28283330	Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement
Q57452991	Using geneid to Identify Genes
Q36288222	Using hiCLIP to identify RNA duplexes that interact with a specific RNA-binding protein.
Q40222516	Using informative Multinomial-Dirichlet prior in a t-mixture with reversible jump estimation of nucleosome positions for genome-wide profiling.
Q42775508	Using normalization to resolve RNA-Seq biases caused by amplification from minimal input.
Q36932681	Using population admixture to help complete maps of the human genome
Q41528289	Using sheep genomes from diverse U.S. breeds to identify missense variants in genes affecting fecundity.
Q47707995	Ustiloxins, fungal cyclic peptides, are ribosomally synthesized in Ustilaginoidea virens.
Q37537497	Utility of B-13 progenitor-derived hepatocytes in hepatotoxicity and genotoxicity studies
Q89968689	Utilizing CRISPR/Cas9 technology to prepare lymphoblastoid cell lines harboring genetic mutations for generating quality control materials in genetic testing
Q28546644	Utilizing Chemical Genomics to Identify Cytochrome b as a Novel Drug Target for Chagas Disease
Q36015724	Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus
Q31107890	VDJviz: a versatile browser for immunogenomics data.
Q34222990	VESPA: software to facilitate genomic annotation of prokaryotic organisms through integration of proteomic and transcriptomic data
Q35766348	VING: a software for visualization of deep sequencing signals
Q49964599	VIPER: a web application for rapid expert review of variant calls.
Q93064287	VIVA (VIsualization of VAriants): A VCF File Visualization Tool
Q41906700	Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens
Q47201395	Validation of Customized Cancer Panel for Detecting Somatic Mutations and Copy Number Alterations.
Q45823548	Validation of a next-generation sequencing assay for clinical molecular oncology.
Q35798854	Validation of a semiconductor next-generation sequencing assay for the clinical genetic screening of CFTR.
Q44145277	Validation of a yeast functional assay for p53 mutations using clonal sequencing
Q30841756	Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population
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P6179	Dimensions Publication ID	1019307928
P356	DOI	10.1038/NBT.1754
P3181	OpenCitations bibliographic resource ID	142568
P932	PMC publication ID	3346182
P698	PubMed publication ID	21221095
P5875	ResearchGate publication ID	49742661

P50	author	Jill P. Mesirov	Q19664665
		Eric Lander	Q970550
		Gad Getz	Q32646381
P2093	author name string	Guttman M
		Robinson JT
		Thorvaldsdóttir H
		Winckler W
P2860	cites work	Integrative analysis of the melanoma transcriptome	Q24608060
		A map of human genome variation from population-scale sequencing	Q24617794
		Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1	Q24651548
		The Integrated Genome Browser: free software for distribution and exploration of genome-scale datasets	Q24655245
		Comprehensive genomic characterization defines human glioblastoma genes and core pathways	Q24656128
		Apollo: a sequence annotation editor	Q24803572
		Artemis: sequence visualization and annotation	Q27861024
		Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals	Q28131802
		The ENCODE (ENCyclopedia Of DNA Elements) Project	Q29547219
		Savant: genome browser for high-throughput sequencing data	Q33609580
		EagleView: a genome assembly viewer for next-generation sequencing technologies	Q36857719
		Visualizing genomes: techniques and challenges	Q37701252
		Tablet--next generation sequence assembly visualization	Q42144683
		MapView: visualization of short reads alignment on a desktop computer	Q43849434
P433	issue	1
P407	language of work or name	English	Q1860
P921	main subject	genomics	Q222046
P304	page(s)	24-6
P577	publication date	2011-01-01
P1433	published in	Nature Biotechnology	Q1893837
P1476	title	Integrative genomics viewer
P478	volume	29

Integrative genomics viewer

scientific article (publication date: 2011)

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