Statistically identifying tumor suppressors and oncogenes from pan-cancer genome-sequencing data.

Citation:

Kumar, R. D., A. C. Searleman, S. J. Swamidass, O. L. Griffith, and R. Bose. Statistically identifying tumor suppressors and oncogenes from pan-cancer genome sequencing data. Bioinformatics, 2015.

Abstract:

Motivation: Several tools exist to identify cancer driver genes based on somatic mutation data. However, these tools do not account for subclasses of cancer genes: oncogenes, which undergo gain-of-function events, and tumor suppressor genes (TSGs) which undergo loss-of-function. A method which accounts for these subclasses could improve performance while also suggesting a mechanism of action for new putative cancer genes.

Results: We develop a panel of five complementary statistical tests and assess their performance against a curated set of 99 HiConf cancer genes using a pan-cancer dataset of 1.7 million mutations. We identify patient bias as a novel signal for cancer gene discovery, and use it to significantly improve detection of oncogenes over existing methods (AUROC = 0.894). Additionally, our test of truncation event rate separates oncogenes and TSGs from one another (AUROC = 0.922). Finally, a random forest integrating the five tests further improves performance and identifies new cancer genes, including CACNG3, HDAC2, HIST1H1E, NXF1, GPS2 and HLA-DRB1.

http://bioinformatics.oxfordjournals.org/content/31/22/3561.abstract