Systematic analysis of somatic mutations in phosphorylation signaling predicts novel cancer drivers

Abstract Large‐scale cancer genome sequencing has uncovered thousands of gene mutations, but distinguishing tumor driver genes from functionally neutral passenger mutations is a major challenge. We analyzed 800 cancer genomes of eight types to find single‐nucleotide variants (SNVs) that precisely ta...

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Bibliographic Details
Main Authors: Jüri Reimand, Gary D Bader
Format: Article
Language:English
Published: Springer Nature 2013-01-01
Series:Molecular Systems Biology
Subjects:
Online Access:https://doi.org/10.1038/msb.2012.68