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GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers

Genome biology · 2011 · Vol. 12(4) · pp. R41–R41
Craig H. MermelSteven E. SchumacherBarbara HillMatthew MeyersonRameen BeroukhimGad Getz

Abstract

We describe methods with enhanced power and specificity to identify genes targeted by somatic copy-number alterations (SCNAs) that drive cancer growth. By separating SCNA profiles into underlying arm-level and focal alterations, we improve the estimation of background rates for each category. We additionally describe a probabilistic method for defining the boundaries of selected-for SCNA regions with user-defined confidence. Here we detail this revised computational approach, GISTIC2.0, and validate its performance in real and simulated datasets.

Cancer Genomics and DiagnosticsMolecular Biology Techniques and ApplicationsGenomic variations and chromosomal abnormalitiesSomatic cellBiologyComputational biologyHuman geneticsCopy-number variationGeneticsGeneGenome

MeSH terms

AlgorithmsComputer SimulationHumansModels, TheoreticalNeoplasmsSoftwareGene DosageComputational BiologyTumor Suppressor Proteins

Funding

  • Doris Duke Charitable Foundation
  • National Institutes of Health
  • National Human Genome Research Institute
  • National Cancer Institute
  • National Institute of General Medical Sciences
Citations
3,797
FWCI
20.43
field-weighted impact
References
44
Percentile
100%
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Citations per year
References
The Hallmarks of Cancer
Cell · 2000 · 28,385 citations
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Journal of the Royal Statistical Society Series B (Statistical Methodology) · 1995 · 106,483 citations
Sequencing technologies — the next generation
Nature Reviews Genetics · 2009 · 7,001 citations
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