Identification of Cancer Driver Modules Based on Graph Clustering from Multiomics Data

被引:1
作者
Zhang, Wei [1 ,2 ]
Wang, Shu-Lin [3 ]
Liu, Yue [3 ]
机构
[1] Changsha Univ, Coll Comp Engn & Appl Math, Changsha, Peoples R China
[2] Changsha Univ, Hunan Prov Key Lab Ind Internet Technol & Secur, Changsha, Peoples R China
[3] Hunan Univ, Coll Comp Sci & Elect Engn, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer driver modules; driver genes; graph clustering; protein-protein interactions; symmetric NMF; MUTUAL EXCLUSIVITY; PATHWAYS; GENES; MUTATION; NETWORK; TUMOR; ALGORITHMS; PHENOTYPE; BREAST; TP53;
D O I
10.1089/cmb.2021.0052
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A major challenge in cancer genomics is to identify cancer driver genes and modules. Most existing methods to identify cancer driver modules (iCDM) identify groups of genes whose somatic mutational patterns exhibit either mutual exclusivity or high coverage of patient samples, without considering other biological information from multiomics data sets. Here we integrate mutual exclusivity, coverage, and protein-protein interaction information to construct an edge-weighted network, and present a graph clustering approach based on symmetric non-negative matrix factorization to iCDM. iCDM was tested on pan-cancer data and the results were compared with those from several advanced computational methods. Our approach outperformed other methods in recovering known cancer driver modules, and the identified driver modules showed high accuracy in classifying normal and tumor samples.
引用
收藏
页码:1007 / 1020
页数:14
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