Title Comprehensive evaluation of computational methods for predicting cancer driver genes
Authors Shi, Xiaohui
Teng, Huajing
Shi, Leisheng
Bi, Wenjian
Wei, Wenqing
Mao, Fengbiao
Sun, Zhongsheng
Affiliation Univ Chinese Acad Sci, Beijing Inst Life Sci, Chinese Acad Sci, Beijing, Peoples R China
Peking Univ, Canc Hosp & Inst, Dept Radiat Oncol, Key LAb Carcinogenesis & Translat Res,Minist Educ, Beijing, Peoples R China
Beijing Inst Genom, Chinese Acad Sci, Key Lab Genom & Precis Med, Beijing, Peoples R China
Peking Univ, Sch Basic Med Sci, Dept Med Genet, Beijing, Peoples R China
Beijing Inst Life Sci, Chinese Acad Sci, Beichen West Rd, Beijing 100101, Peoples R China
Peking Univ Third Hosp, Inst Med Innovat & Res, Huayuan North Rd, Beijing 100080, Peoples R China
Univ Chinese Acad Sci, Beijing Inst Life Sci, Chinese Acad Sci, CAS Ctr Excellence Biot Interact, Beijing, Peoples R China
Univ Chinese Acad Sci, State Key Lab Integrated Management Pest Insects, Inst Genom Med,Zhejiang Canc Hosp,Inst Basic Med, Wenzhou Med Univ,IBMC BGI Ctr,Canc Hosp, Beijing, Peoples R China
Keywords SOMATIC MUTATIONS
NETWORK
GENOME
DISCOVERY
Issue Date 10-Mar-2022
Publisher BRIEFINGS IN BIOINFORMATICS
Abstract Optimal methods could effectively improve the accuracy of predicting and identifying candidate driver genes. Various computational methods based on mutational frequency, network and function approaches have been developed to identify mutation driver genes in cancer genomes. However, a comprehensive evaluation of the performance levels of network-, function- and frequency-based methods is lacking. In the present study, we assessed and compared eight performance criteria for eight network-based, one function-based and three frequency-based algorithms using eight benchmark datasets. Under different conditions, the performance of approaches varied in terms of network, measurement and sample size. The frequency-based driverMAPS and network-based HotNet2 methods showed the best overall performance. Network-based algorithms using protein-protein interaction networks outperformed the function- and the frequency-based approaches. Precision, F1 score and Matthews correlation coefficient were low for most approaches. Thus, most of these algorithms require stringent cutoffs to correctly distinguish driver and non-driver genes. We constructed a website named Cancer Driver Catalog (http://159.226.67.237/sun/cancer_driver/), wherein we integrated the gene scores predicted by the foregoing software programs. This resource provides valuable guidance for cancer researchers and clinical oncologists prioritizing cancer driver gene candidates by using an optimal tool.
URI http://hdl.handle.net/20.500.11897/647240
ISSN 1467-5463
DOI 10.1093/bib/bbab548
Indexed SCI(E)
Appears in Collections: 北京肿瘤医院
基础医学院
第三医院

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