JISTIC: identification of significant targets in cancer.

scientific article

JISTIC: identification of significant targets in cancer. is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P8978DBLP publication IDjournals/bmcbi/Sanchez-GarciaAMP10
P6179Dimensions Publication ID1011737467
P356DOI10.1186/1471-2105-11-189
P2888exact matchhttps://scigraph.springernature.com/pub.10.1186/1471-2105-11-189
P932PMC publication ID2873534
P698PubMed publication ID20398270
P5875ResearchGate publication ID43180903

P50authorUri David AkaviaQ81195402
Dana Pe'erQ16204043
P2093author name stringEyal Mozes
Felix Sanchez-Garcia
P2860cites workGene ontology: tool for the unification of biologyQ23781406
A novel GDNF-inducible gene, BMZF3, encodes a transcriptional repressor associated with KAP-1Q24302259
HIRA, the human homologue of yeast Hir1p and Hir2p, is a novel cyclin-cdk2 substrate whose expression blocks S-phase progressionQ24551005
Gene expression profiling predicts clinical outcome of prostate cancerQ24594253
A census of human cancer genesQ24647081
Characterizing the cancer genome in lung adenocarcinomaQ24649926
Comprehensive genomic characterization defines human glioblastoma genes and core pathwaysQ24656128
Identification and characterization of EBP, a novel EEN binding protein that inhibits Ras signaling and is recruited into the nucleus by the MLL-EEN fusion proteinQ28208684
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastomaQ28237604
CDK8 is a colorectal cancer oncogene that regulates beta-catenin activityQ28294122
Assessing the significance of chromosomal aberrations in cancer: methodology and application to gliomaQ30014823
Analysis of array CGH data: from signal ratio to gain and loss of DNA regionsQ30961366
Functional copy-number alterations in cancerQ33368629
Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumorsQ34190883
Gene expression profiling separates chromophobe renal cell carcinoma from oncocytoma and identifies vesicular transport and cell junction proteins as differentially expressed genes.Q34587288
Nuclear factor 45 (NF45) is a regulatory subunit of complexes with NF90/110 involved in mitotic controlQ36748114
Inhibitor of differentiation 4 drives brain tumor-initiating cell genesis through cyclin E and notch signalingQ36802989
Fibulin 1 is downregulated through promoter hypermethylation in gastric cancerQ37023915
Integrated genomic profiling of endometrial carcinoma associates aggressive tumors with indicators of PI3 kinase activationQ37140110
Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE.Q37160880
The urokinase receptor and its structural homologue C4.4A in human cancer: expression, prognosis and pharmacological inhibitionQ37294301
Polypyrimidine tract binding protein regulates IRES-mediated gene expression during apoptosisQ38310976
A CD147-targeting siRNA inhibits the proliferation, invasiveness, and VEGF production of human malignant melanoma cells by down-regulating glycolysisQ39941968
Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A-TCRAD juxtapositionQ47694238
P275copyright licenseCreative Commons Attribution 2.0 GenericQ19125117
P6216copyright statuscopyrightedQ50423863
P304page(s)189
P577publication date2010-04-14
P1433published inBMC BioinformaticsQ4835939
P1476titleJISTIC: identification of significant targets in cancer
P478volume11

Reverse relations

cites work (P2860)
Q30654515A genomic random interval model for statistical analysis of genomic lesion data
Q30570534A high-throughput computational framework for identifying significant copy number aberrations from array comparative genomic hybridisation data
Q39896921A method for generating new datasets based on copy number for cancer analysis
Q40366176A scale-space method for detecting recurrent DNA copy number changes with analytical false discovery rate control
Q28394747A systematic comparison of copy number alterations in four types of female cancer
Q34453995An integrated approach to uncover drivers of cancer.
Q28487526An integrative genomic and transcriptomic analysis reveals potential targets associated with cell proliferation in uterine leiomyomas
Q34534035Comparative analysis of methods for identifying recurrent copy number alterations in cancer
Q34979403Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discovery
Q41145800DEOD: uncovering dominant effects of cancer-driver genes based on a partial covariance selection method
Q38265995Deciphering oncogenic drivers: from single genes to integrated pathways
Q33760431Detecting independent and recurrent copy number aberrations using interval graphs
Q35557782GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers
Q55714851Germline and somatic variations influence the somatic mutational signatures of esophageal squamous cell carcinomas in a Chinese population.
Q38645510Hypodontia, a prospective predictive marker for tumor?
Q89077811Identifying disease-associated copy number variations by a doubly penalized regression model
Q37689928Identifying driver mutations in sequenced cancer genomes: computational approaches to enable precision medicine
Q50088009Ligand-activated BMP signaling inhibits cell differentiation and death to promote melanoma.
Q43090167MelanomaDB: A Web Tool for Integrative Analysis of Melanoma Genomic Information to Identify Disease-Associated Molecular Pathways
Q99350211Probability distribution of copy number alterations along the genome: an algorithm to distinguish different tumour profiles
Q37248289RHPN2 drives mesenchymal transformation in malignant glioma by triggering RhoA activation
Q39616819RUBIC identifies driver genes by detecting recurrent DNA copy number breaks
Q35008652SubPatCNV: approximate subspace pattern mining for mapping copy-number variations
Q35032523The landscape of candidate driver genes differs between male and female breast cancer
Q42182370Trans-ancestry mutational landscape of hepatocellular carcinoma genomes
Q36833326Transposon mutagenesis identifies genetic drivers of Braf(V600E) melanoma
Q35051828Uncover disease genes by maximizing information flow in the phenome-interactome network

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