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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.
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Craig H. Mermel
Steven E. Schumacher
Barbara Hill
Genome biology
Dana-Farber Cancer Institute
Broad Institute
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Mermel et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69da11319a6164e50fa3db8a — DOI: https://doi.org/10.1186/gb-2011-12-4-r41
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