| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1031680869 |
| P356 | DOI | 10.1186/GB-2009-10-3-R32 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1186/gb-2009-10-3-r32 |
| P932 | PMC publication ID | 2691003 |
| P698 | PubMed publication ID | 19327155 |
| P5875 | ResearchGate publication ID | 24239681 |
| P50 | author | Eric J. Topol | Q5387640 |
| Nicholas J Schork | Q63005429 | ||
| Olivier Harismendy | Q64355285 | ||
| Timothy B Stockwell | Q89222480 | ||
| Samuel Levy | Q98464377 | ||
| P2093 | author name string | Karen Y Beeson | |
| Pauline C Ng | |||
| Robert L Strausberg | |||
| Xiaoyun Wang | |||
| Kelly A Frazer | |||
| Sarah S Murray | |||
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| P433 | issue | 3 | |
| P304 | page(s) | R32 | |
| P577 | publication date | 2009-03-27 | |
| P1433 | published in | Genome Biology | Q5533480 |
| P1476 | title | Evaluation of next generation sequencing platforms for population targeted sequencing studies | |
| P478 | volume | 10 |
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| Q38002079 | A review of the application of molecular genetics for fisheries management and conservation of sharks and rays. |
| Q33729176 | A sweet potato gene index established by de novo assembly of pyrosequencing and Sanger sequences and mining for gene-based microsatellite markers |
| Q34055287 | A wide extent of inter-strain diversity in virulent and vaccine strains of alphaherpesviruses |
| Q33948981 | ADaM: augmenting existing approximate fast matching algorithms with efficient and exact range queries |
| Q37694285 | AMD biofilms: using model communities to study microbial evolution and ecological complexity in nature. |
| Q33530810 | Accurate detection and genotyping of SNPs utilizing population sequencing data |
| Q37141323 | Alterations in the Fecal Microbiota of Patients with HIV-1 Infection: An Observational Study in A Chinese Population. |
| Q35896989 | An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia |
| Q47105018 | An efficient error correction algorithm using FM-index |
| Q30863381 | An evaluation of alternative methods for constructing phylogenies from whole genome sequence data: a case study with Salmonella |
| Q34538741 | An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data |
| Q37893042 | An introduction to the medicinal plant genome project |
| Q54970332 | Analysis of LCT-13910 genotypes and bone mineral density in ancient skeletal materials. |
| Q34207464 | Analysis of high-depth sequence data for studying viral diversity: a comparison of next generation sequencing platforms using Segminator II. |
| Q28293359 | Analysis of next-generation genomic data in cancer: accomplishments and challenges |
| Q33659736 | Analysis of plant microbe interactions in the era of next generation sequencing technologies |
| Q33803455 | Annotation-based genome-wide SNP discovery in the large and complex Aegilops tauschii genome using next-generation sequencing without a reference genome sequence |
| Q37856448 | Application of SNPs for population genetics of nonmodel organisms: new opportunities and challenges |
| Q38149683 | Application of high-throughput sequencing for studying genomic variations in congenital heart disease |
| Q37739034 | Application of second-generation sequencing to cancer genomics |
| Q35600172 | Applications of next-generation sequencing technologies to diagnostic virology |
| Q42921943 | Are nucleosome positions in vivo primarily determined by histone-DNA sequence preferences? |
| Q33538377 | Assembly algorithms for next-generation sequencing data |
| Q35085282 | Association studies for next-generation sequencing |
| Q35179812 | Bacterial diversity assessment in Antarctic terrestrial and aquatic microbial mats: a comparison between bidirectional pyrosequencing and cultivation |
| Q50862043 | Bayexer: an accurate and fast Bayesian demultiplexer for Illumina sequences. |
| Q38245512 | Best practices for mapping replication origins in eukaryotic chromosomes |
| Q36736003 | Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized Medicine |
| Q37623244 | Bioinformatics approaches for genomics and post genomics applications of next-generation sequencing |
| Q38796894 | Biomechanisms of Comorbidity: Reviewing Integrative Analyses of Multi-omics Datasets and Electronic Health Records |
| Q99974697 | Brevipalpus oncidii, a new record for Australia, is not a vector ofOrchid fleck virus |
| Q30671080 | Calculation of Tajima's D and other neutrality test statistics from low depth next-generation sequencing data. |
| Q28386910 | Capillary electrophoresis applied to DNA: determining and harnessing sequence and structure to advance bioanalyses (2009-2014) |
| Q41169504 | Catharanthus mosaic virus: A potyvirus from a gymnosperm, Welwitschia mirabilis. |
| Q43891611 | Challenges and opportunities for next-generation sequencing in companion diagnostics |
| Q28727944 | Challenges and opportunities in estimating viral genetic diversity from next-generation sequencing data |
| Q28596030 | Challenges of Identifying Clinically Actionable Genetic Variants for Precision Medicine |
| Q35126739 | Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder |
| Q33931064 | Characterization of single-nucleotide variation in Indian-origin rhesus macaques (Macaca mulatta) |
| Q30670347 | Characterizing Benzo[a]pyrene-induced lacZ mutation spectrum in transgenic mice using next-generation sequencing. |
| Q30635784 | Characterizing and measuring bias in sequence data |
| Q33962447 | Characterizing homologues of crop domestication genes in poorly described wild relatives by high-throughput sequencing of whole genomes. |
| Q43805410 | Chloroplast genome sequences from total DNA for plant identification. |
| Q41070627 | Chromatin immunoprecipitation and an open chromatin assay in zebrafish erythrocytes |
| Q36460959 | Chromatin immunoprecipitation in adult zebrafish red cells |
| Q36361047 | Clinical implications of human population differences in genome-wide rates of functional genotypes |
| Q36343255 | Clinical integration of next-generation sequencing technology |
| Q53547425 | Clinical investigational studies for validation of a next-generation sequencing in vitro diagnostic device for cystic fibrosis testing. |
| Q30480627 | Combining next-generation sequencing strategies for rapid molecular resource development from an invasive aphid species, Aphis glycines |
| Q34526801 | Coming of age: ten years of next-generation sequencing technologies |
| Q35076798 | Comparative analyses of two Geraniaceae transcriptomes using next-generation sequencing |
| Q36335799 | Comparative transcriptomics of Entelegyne spiders (Araneae, Entelegynae), with emphasis on molecular evolution of orphan genes |
| Q41955064 | Comparative transcriptomics of two environmentally relevant cyanobacteria reveals unexpected transcriptome diversity |
| Q30580412 | Comparison of mapping algorithms used in high-throughput sequencing: application to Ion Torrent data. |
| Q33911299 | Comparison of sequence reads obtained from three next-generation sequencing platforms |
| Q34584099 | Comparison of sequencing platforms for single nucleotide variant calls in a human sample |
| Q33908627 | Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes. |
| Q28740628 | Comparison of three targeted enrichment strategies on the SOLiD sequencing platform |
| Q34397126 | Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing. |
| Q28472992 | Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset |
| Q37618538 | Computational methods for discovering structural variation with next-generation sequencing |
| Q37974462 | Computer simulations: tools for population and evolutionary genetics |
| Q36131933 | Contamination-controlled high-throughput whole genome sequencing for influenza A viruses using the MiSeq sequencer |
| Q42869231 | Contribution of histone sequence preferences to nucleosome organization: proposed definitions and methodology |
| Q34298942 | Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens' theorem |
| Q38222395 | Critical review of NGS analyses for de novo genotyping multigene families. |
| Q35693617 | Current genetic methodologies in the identification of disaster victims and in forensic analysis |
| Q42013233 | Cytoplasmic intron sequence-retaining transcripts can be dendritically targeted via ID element retrotransposons |
| Q42644433 | DIVERGENOME: a bioinformatics platform to assist population genetics and genetic epidemiology studies |
| Q38616674 | De Novo Assembly of Complete Chloroplast Genomes from Non-model Species Based on a K-mer Frequency-Based Selection of Chloroplast Reads from Total DNA Sequences. |
| Q64078904 | De novo transcriptome and phytochemical analyses reveal differentially expressed genes and characteristic secondary metabolites in the original oolong tea (Camellia sinensis) cultivar 'Tieguanyin' compared with cultivar 'Benshan' |
| Q35497611 | De novo transcriptome assembly of the wild relative of tea tree (Camellia taliensis) and comparative analysis with tea transcriptome identified putative genes associated with tea quality and stress response |
| Q33847120 | Decoding a substantial set of samples in parallel by massive sequencing |
| Q34774744 | Delivery of a clinical genomics service |
| Q37055268 | Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing |
| Q41815975 | Detecting copy number variation with mated short reads |
| Q41789320 | Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes |
| Q28082859 | Detection of Genomic Structural Variants from Next-Generation Sequencing Data |
| Q34251415 | Determination of RET Sequence Variation in an MEN2 Unaffected Cohort Using Multiple-Sample Pooling and Next-Generation Sequencing |
| Q41807657 | Development and assessment of an optimized next-generation DNA sequencing approach for the mtgenome using the Illumina MiSeq |
| Q34989518 | Development of genetic markers in Eucalyptus species by target enrichment and exome sequencing |
| Q35053373 | Development of reference transcriptomes for the major field insect pests of cowpea: a toolbox for insect pest management approaches in west Africa |
| Q57899034 | Diagnostic applications of next generation sequencing: working towards quality standards/Diagnostische Anwendung von Next Generation Sequencing: Auf dem Weg zu Qualitätsstandards |
| Q34550157 | Differences in sequencing technologies improve the retrieval of anammox bacterial genome from metagenomes |
| Q43640848 | Different mutations in PDE4D associated with developmental disorders with mirror phenotypes. |
| Q35021617 | Differential expression of tomato spotted wilt virus-derived viral small RNAs in infected commercial and experimental host plants |
| Q21267194 | Discovery and characterization of medaka miRNA genes by next generation sequencing platform |
| Q28741663 | Distinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individual |
| Q31004396 | Diversifying crops for food and nutrition security - a case of teff. |
| Q28742103 | Dynamic evolution of base composition: causes and consequences in avian phylogenomics |
| Q33742574 | EXCAVATOR: detecting copy number variants from whole-exome sequencing data |
| Q35549634 | Effect of the enzyme and PCR conditions on the quality of high-throughput DNA sequencing results |
| Q35795078 | Efficient study design for next generation sequencing |
| Q38609944 | Epidemiology of Patients with Ovarian Cancer with and Without a BRCA1/2 Mutation |
| Q30659610 | Estimating DNA polymorphism from next generation sequencing data with high error rate by dual sequencing applications |
| Q36320414 | Estimating error models for whole genome sequencing using mixtures of Dirichlet-multinomial distributions |
| Q33929681 | Estimation of allele frequency and association mapping using next-generation sequencing data |
| Q33839369 | Evaluation and optimisation of indel detection workflows for ion torrent sequencing of the BRCA1 and BRCA2 genes |
| Q42398314 | Evaluation of second-generation sequencing of 19 dilated cardiomyopathy genes for clinical applications |
| Q26745956 | Evaluation of the methods to identify patients who may benefit from PARP inhibitor use |
| Q38263750 | Evidence against a genomic code for nucleosome positioning. Reply to "Nucleosome sequence preferences influence in vivo nucleosome organization.". |
| Q37983903 | Evolutionary insight from whole-genome sequencing of experimentally evolved microbes. |
| Q30426901 | Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families |
| Q38217346 | Exome sequencing: new insights into lipoprotein disorders |
| Q55363718 | Feasibility study of cancer genome alterations identified by next generation sequencing: ABC study. |
| Q35946687 | Finding the right coverage: the impact of coverage and sequence quality on single nucleotide polymorphism genotyping error rates. |
| Q35101684 | Finishing bacterial genome assemblies with Mix. |
| Q31137675 | From next-generation resequencing reads to a high-quality variant data set. |
| Q42223305 | Full-Genome Sequencing of Four Bluetongue Virus Serotype 11 Viruses |
| Q36744986 | Functional Annotation and Comparative Analysis of a Zygopteran Transcriptome |
| Q30915634 | G-CNV: A GPU-Based Tool for Preparing Data to Detect CNVs with Read-Depth Methods. |
| Q31164412 | GLM-based optimization of NGS data analysis: A case study of Roche 454, Ion Torrent PGM and Illumina NextSeq sequencing data |
| Q41537361 | Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis |
| Q51381984 | Genetic analysis of the PKHD1 gene with long-rang PCR sequencing. |
| Q35917791 | Genetic markers, genotyping methods & next generation sequencing in Mycobacterium tuberculosis |
| Q90612603 | Genome sequence of Jatropha curcas L., a non-edible biodiesel plant, provides a resource to improve seed-related traits |
| Q35451892 | Genome-based analysis of the nonhuman primate Macaca fascicularis as a model for drug safety assessment |
| Q38450442 | Genome-wide SNP discovery in mungbean by Illumina HiSeq |
| Q33814805 | Genome-wide association studies in cancer--current and future directions |
| Q35493806 | Genome-wide depletion of replication initiation events in highly transcribed regions |
| Q29616767 | Genome-wide genetic marker discovery and genotyping using next-generation sequencing |
| Q28727988 | Genomic diversity in switchgrass (Panicum virgatum): from the continental scale to a dune landscape |
| Q28732333 | Genomic sequencing in clinical trials |
| Q33903792 | Genotype and SNP calling from next-generation sequencing data |
| Q47554103 | Germline contamination and leakage in whole genome somatic single nucleotide variant detection. |
| Q30533580 | Global analysis of disease-related DNA sequence variation in 10 healthy individuals: implications for whole genome-based clinical diagnostics |
| Q34074180 | Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping |
| Q33918160 | Going deeper: metagenome of a hadopelagic microbial community |
| Q34227250 | Graph accordance of next-generation sequence assemblies |
| Q36094871 | High Resolution Genomic Scans Reveal Genetic Architecture Controlling Alcohol Preference in Bidirectionally Selected Rat Model |
| Q28728910 | High accuracy mutation detection in leukemia on a selected panel of cancer genes |
| Q34382818 | High level of structural polymorphism driven by mobile elements in the Hox genomic region of the Chaetognath Spadella cephaloptera |
| Q34835141 | High-quality DNA sequence capture of 524 disease candidate genes |
| Q40015135 | High-resolution mapping of evolutionary trajectories in a phage |
| Q33821609 | High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum |
| Q47744693 | High-throughput and parallel SNP discovery in selected candidate genes in Eucalyptus camaldulensis using Illumina NGS platform. |
| Q36094684 | High-throughput molecular diagnosis of von Willebrand disease by next generation sequencing methods |
| Q28537728 | High-throughput sequencing and mutagenesis to accelerate the domestication of Microlaena stipoides as a new food crop |
| Q34328777 | High-throughput sequencing of microdissected chromosomal regions |
| Q58514499 | How does sequence variability affectde novoassembly quality? |
| Q21245451 | Human genetics and genomics a decade after the release of the draft sequence of the human genome |
| Q35547093 | Hybrid De Novo Genome Assembly Using MiSeq and SOLiD Short Read Data |
| Q36023199 | Identical consensus sequence and conserved genomic polymorphism of hepatitis E virus during controlled interspecies transmission |
| Q36233290 | Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia |
| Q24622594 | Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens |
| Q54413738 | Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males |
| Q30617713 | Identification of optimum sequencing depth especially for de novo genome assembly of small genomes using next generation sequencing data |
| Q34474098 | Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing |
| Q39113925 | Identifying Y-chromosomal diversity by long-template PCR. |
| Q33806845 | Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders |
| Q42688195 | Impact of the next generation DNA sequencers. |
| Q31132377 | Improved Efficiency and Reliability of NGS Amplicon Sequencing Data Analysis for Genetic Diagnostic Procedures Using AGSA Software. |
| Q35563550 | Improved lower bounds of DNA tags based on a modified genetic algorithm |
| Q41018539 | Improving draft assemblies by iterative mapping and assembly of short reads to eliminate gaps |
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| Q33575553 | Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample |
| Q47113700 | Integration of omics sciences to advance biology and medicine. |
| Q47586484 | Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing |
| Q31088871 | Large-scale candidate gene scan reveals the role of chemoreceptor genes in host plant specialization and speciation in the pea aphid |
| Q40088946 | Local sequence and sequencing depth dependent accuracy of RNA-seq reads |
| Q89820805 | MAC: Merging Assemblies by Using Adjacency Algebraic Model and Classification |
| Q35171439 | MHC class II variation in a rare and ecological specialist mouse lemur reveals lower allelic richness and contrasting selection patterns compared to a generalist and widespread sympatric congener |
| Q90458341 | Macrogeographic genetic structure of Lutzomyia longipalpis complex populations using Next Generation Sequencing |
| Q38773403 | Mapping rare and common causal alleles for complex human diseases |
| Q33720716 | Marine genomics: at the interface of marine microbial ecology and biodiscovery |
| Q45876564 | Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis |
| Q36015586 | MetaBAT, an efficient tool for accurately reconstructing single genomes from complex microbial communities |
| Q41866289 | MetaSeq: privacy preserving meta-analysis of sequencing-based association studies |
| Q47702078 | Metabarcoding analysis of eukaryotic microbiota in the gut of HIV-infected patients |
| Q33555871 | Metagenome of the Mediterranean deep chlorophyll maximum studied by direct and fosmid library 454 pyrosequencing |
| Q43791398 | Metagenomic 16S rDNA Illumina tags are a powerful alternative to amplicon sequencing to explore diversity and structure of microbial communities |
| Q56855243 | Metagenomics: The Paths Forward |
| Q30953199 | Metagenomics: tools and insights for analyzing next-generation sequencing data derived from biodiversity studies |
| Q26859692 | Microarray resources for genetic and genomic studies in chicken: a review |
| Q30481756 | Microdroplet-based PCR enrichment for large-scale targeted sequencing |
| Q33530434 | Microindel detection in short-read sequence data |
| Q34484555 | Microsatellite abundance across the Anthozoa and Hydrozoa in the phylum Cnidaria. |
| Q34592702 | Microsatellites for next-generation ecologists: a post-sequencing bioinformatics pipeline. |
| Q33680419 | Mitochondrial DNA variant discovery and evaluation in human Cardiomyopathies through next-generation sequencing |
| Q51602781 | Mitochondrial and nuclear DNA sequences reveal recent divergence in morphologically indistinguishable petrels. |
| Q34257967 | Mitochondrial genome evolution in species belonging to the Phialocephala fortinii s.l. - Acephala applanata species complex |
| Q30574430 | Modeling read counts for CNV detection in exome sequencing data |
| Q34405611 | Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures |
| Q35756084 | Monitoring Spawning Activity in a Southern California Marine Protected Area Using Molecular Identification of Fish Eggs |
| Q92949774 | Multi gene panel testing for hereditary breast cancer - is it ready to be used? |
| Q21092720 | Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis |
| Q34070547 | Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database development |
| Q34746989 | Multiplex target capture with double-stranded DNA probes |
| Q37015462 | Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing. |
| Q92323632 | Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma |
| Q55001264 | Natural antisense transcripts in plants: a review and identification in soybean infected with Phakopsora pachyrhizi SuperSAGE library. |
| Q42041386 | NeSSM: a Next-generation Sequencing Simulator for Metagenomics |
| Q34698830 | New SNPs for population genetic analysis reveal possible cryptic speciation of eastern Australian sea mullet (Mugil cephalus). |
| Q27026914 | New virologic tools for management of chronic hepatitis B and C |
| Q27690994 | Next generation sequencing applications for breast cancer research. |
| Q34340835 | Next generation sequencing for TCR repertoire profiling: platform-specific features and correction algorithms. |
| Q30474368 | Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology |
| Q39120229 | Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions |
| Q38679306 | Next-Generation Sequencing and Applications to the Diagnosis and Treatment of Lung Cancer |
| Q41747887 | Next-Generation Sequencing: The Translational Medicine Approach from "Bench to Bedside to Population". |
| Q34238930 | Next-generation sequencing for cancer diagnostics: a practical perspective. |
| Q38689095 | Next-generation sequencing for endocrine cancers: Recent advances and challenges |
| Q38944792 | Next-generation sequencing in neuromuscular diseases |
| Q38061737 | Next-generation sequencing in the clinic: promises and challenges |
| Q33744262 | Next-generation sequencing: a transformative tool for vaccinology |
| Q47107418 | Next-generation sequencing: recent applications to the analysis of colorectal cancer. |
| Q34382486 | Not all sequence tags are created equal: designing and validating sequence identification tags robust to indels |
| Q34241325 | Nucleosome depletion at yeast terminators is not intrinsic and can occur by a transcriptional mechanism linked to 3'-end formation |
| Q34976936 | Nucleosome free regions in yeast promoters result from competitive binding of transcription factors that interact with chromatin modifiers. |
| Q48064573 | Orthologous comparisons of the Hd1 region across genera reveal Hd1 gene lability within diploid Oryza species and disruptions to microsynteny in Sorghum |
| Q92205128 | PattRec: An easy-to-use CNV detection tool optimized for targeted NGS assays with diagnostic purposes |
| Q42616043 | Phenotype sequencing: identifying the genes that cause a phenotype directly from pooled sequencing of independent mutants |
| Q33497121 | Photosystem I gene cassettes are present in marine virus genomes |
| Q34587451 | Phred-Phrap package to analyses tools: a pipeline to facilitate population genetics re-sequencing studies |
| Q38997815 | Phylogenetic Heatmaps Highlight Composition Biases in Sequenced Reads |
| Q33801716 | PileLine: a toolbox to handle genome position information in next-generation sequencing studies |
| Q58069564 | Population Genetics in Nonmodel Organisms: II. Natural Selection in Marginal Habitats Revealed by Deep Sequencing on Dual Platforms |
| Q30572210 | Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation |
| Q35167237 | Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level |
| Q39877836 | Power of deep sequencing and agilent microarray for gene expression profiling study |
| Q34475820 | Pre-capture multiplexing improves efficiency and cost-effectiveness of targeted genomic enrichment |
| Q34195606 | Producing parasitic helminth reference and draft genomes at the Wellcome Trust Sanger Institute. |
| Q37067731 | Pronounced genetic differentiation and recent secondary contact in the mangrove tree Lumnitzera racemosa revealed by population genomic analyses |
| Q34955033 | Protocol matters: which methylome are you actually studying? |
| Q30558763 | Qualimap: evaluating next-generation sequencing alignment data. |
| Q37380422 | Quantifying adaptive evolution in the Drosophila immune system |
| Q34389440 | Quantitative analysis of focused a-to-I RNA editing sites by ultra-high-throughput sequencing in psychiatric disorders |
| Q42720622 | RADSeq: next-generation population genetics |
| Q33807870 | RAIphy: phylogenetic classification of metagenomics samples using iterative refinement of relative abundance index profiles |
| Q33983478 | RAMICS: trainable, high-speed and biologically relevant alignment of high-throughput sequencing reads to coding DNA. |
| Q35618848 | Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer |
| Q34945544 | Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification |
| Q37971383 | Read count approach for DNA copy number variants detection |
| Q34442752 | Read length versus depth of coverage for viral quasispecies reconstruction |
| Q33349484 | Reconstructing a puzzle: existence of cyanophages containing both photosystem-I and photosystem-II gene suites inferred from oceanic metagenomic datasets |
| Q41868170 | Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes |
| Q28475554 | Reference-free validation of short read data |
| Q34381743 | Replication strategies for rare variant complex trait association studies via next-generation sequencing |
| Q35681314 | Reproducibility of Variant Calls in Replicate Next Generation Sequencing Experiments |
| Q34660514 | Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence |
| Q37676763 | Reverse genetics techniques: engineering loss and gain of gene function in plants |
| Q36268758 | RiboTagger: fast and unbiased 16S/18S profiling using whole community shotgun metagenomic or metatranscriptome surveys |
| Q35631070 | Role of DNA profiling in forensic odontology |
| Q40647488 | SNP Formation Bias in the Murine Genome Provides Evidence for Parallel Evolution |
| Q30000842 | SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data |
| Q34994388 | SNP discovery by illumina-based transcriptome sequencing of the olive and the genetic characterization of Turkish olive genotypes revealed by AFLP, SSR and SNP markers |
| Q34924967 | SNP discovery in European anchovy (Engraulis encrasicolus, L) by high-throughput transcriptome and genome sequencing |
| Q51036016 | SNP discovery in nonmodel organisms: strand bias and base-substitution errors reduce conversion rates. |
| Q33588854 | SNP discovery performance of two second-generation sequencing platforms in the NOD2 gene region |
| Q31081414 | SNP discovery using Next Generation Transcriptomic Sequencing in Atlantic herring (Clupea harengus) |
| Q37680742 | Selection and mutation in the "new" genetics: an emerging hypothesis. |
| Q34023328 | Selection in coastal Synechococcus (cyanobacteria) populations evaluated from environmental metagenomes |
| Q33631203 | Semi-automated library preparation for high-throughput DNA sequencing platforms |
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