OncodriveCLUSTL: a sequence-based clustering method to identify cancer drivers

被引:48
作者
Arnedo-Pac, Claudia [1 ]
Mularoni, Loris [1 ]
Muinos, Ferran [1 ]
Gonzalez-Perez, Abel [1 ,2 ]
Lopez-Bigas, Nuria [1 ,2 ,3 ]
机构
[1] Barcelona Inst Sci & Technol, Inst Res Biomed IRB Barcelona, Barcelona, Spain
[2] Univ Pompeu Fabra, Res Program Biomed Informat, Barcelona, Spain
[3] ICREA, Passeig Lluis Companys 23, Barcelona 08010, Spain
基金
欧洲研究理事会;
关键词
CHROMATIN ORGANIZATION; SOMATIC MUTATIONS;
D O I
10.1093/bioinformatics/btz501
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Identification of the genomic alterations driving tumorigenesis is one of the main goals in oncogenomics research. Given the evolutionary principles of cancer development, computational methods that detect signals of positive selection in the pattern of tumor mutations have been effectively applied in the search for cancer genes. One of these signals is the abnormal clustering of mutations, which has been shown to be complementary to other signals in the detection of driver genes. Results: We have developed OncodriveCLUSTL, a new sequence-based clustering algorithm to detect significant clustering signals across genomic regions. OncodriveCLUSTL is based on a local background model derived from the simulation of mutations accounting for the composition of tri- or penta-nucleotide context substitutions observed in the cohort under study. Our method can identify known clusters and bona-fide cancer drivers across cohorts of tumor whole-exomes, outperforming the existing OncodriveCLUST algorithm and complementing other methods based on different signals of positive selection. Our results indicate that OncodriveCLUSTL can be applied to the analysis of non-coding genomic elements and non-human mutations data.
引用
收藏
页码:4788 / 4790
页数:3
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