Somatic selection distinguishes oncogenes and tumor suppressor genes
Genre
Journal ArticleDate
2020-01-01Author
Chandrashekar, PAhmadinejad, N
Wang, J
Sekulic, A
Egan, JB
Asmann, YW
Kumar, S
Maley, C
Liu, L
Permanent link to this record
http://hdl.handle.net/20.500.12613/4523
Metadata
Show full item recordDOI
10.1093/bioinformatics/btz851Abstract
© The Author(s) 2019. Motivation: Functions of cancer driver genes vary substantially across tissues and organs. Distinguishing passenger genes, oncogenes (OGs) and tumor-suppressor genes (TSGs) for each cancer type is critical for understanding tumor biology and identifying clinically actionable targets. Although many computational tools are available to predict putative cancer driver genes, resources for context-aware classifications of OGs and TSGs are limited. Results: We show that the direction and magnitude of somatic selection of protein-coding mutations are significantly different for passenger genes, OGs and TSGs. Based on these patterns, we develop a new method (genes under selection in tumors) to discover OGs and TSGs in a cancer-type specific manner. Genes under selection in tumors shows a high accuracy (92%) when evaluated via strict cross-validations. Its application to 10 172 tumor exomes found known and novel cancer drivers with high tissue-specificities. In 11 out of 13 OGs shared among multiple cancer types, we found functional domains selectively engaged in different cancers, suggesting differences in disease mechanisms.Citation to related work
Oxford University Press (OUP)Has part
BioinformaticsADA compliance
For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.eduae974a485f413a2113503eed53cd6c53
http://dx.doi.org/10.34944/dspace/4505