Identification of driver modules in pan-cancer via coordinating coverage and exclusivity

被引:13
|
作者
Gao, Bo [1 ,2 ]
Li, Guojun [1 ,2 ]
Liu, Juntao [1 ]
Li, Yang [1 ]
Huang, Xiuzhen [2 ,3 ]
机构
[1] Shandong Univ, Sch Math, Jinan 250100, Shandong, Peoples R China
[2] Arkansas State Univ, Dept Comp Sci, Jonesboro, AR 72401 USA
[3] Arkansas State Univ, Mol Biosci Program, Jonesboro, AR 72401 USA
基金
美国国家科学基金会;
关键词
pan-cancer; coverage; exclusivity; driver gene; network module; MUTUAL EXCLUSIVITY; SOMATIC MUTATIONS; PATHWAYS; PATTERNS; COMBINATIONS; GENES;
D O I
10.18632/oncotarget.16433
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is widely accepted that cancer is driven by accumulated somatic mutations during the lifetime of an individual. Cancer mutations may target relatively small number of cell functional modules. The heterogeneity in different cancer patients makes it difficult to identify driver mutations or functional modules related to cancer. It is biologically desired to be capable of identifying cancer pathway modules through coordination between coverage and exclusivity. There have been a few approaches developed for this purpose, but they all have limitations in practice due to their computational complexity and prediction accuracy. We present a network based approach, CovEx, to predict the specific patient oriented modules by 1) discovering candidate modules for each considered gene, 2) extracting significant candidates by harmonizing coverage and exclusivity and, 3) further selecting the patient oriented modules based on a set cover model. Applying CovEx to pan-cancer datasets spanning 12 cancer types collecting from public database TCGA, it demonstrates significant superiority over the current leading competitors in performance. It is published under GNU GENERAL PUBLIC LICENSE and the source code is available at: https://sourceforge.net/projects/cancer-pathway/files/.
引用
收藏
页码:36115 / 36126
页数:12
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