Identification of cancer driver genes based on nucleotide context.
Ontology highlight
ABSTRACT: Cancer genomes contain large numbers of somatic mutations but few of these mutations drive tumor development. Current approaches either identify driver genes on the basis of mutational recurrence or approximate the functional consequences of nonsynonymous mutations by using bioinformatic scores. Passenger mutations are enriched in characteristic nucleotide contexts, whereas driver mutations occur in functional positions, which are not necessarily surrounded by a particular nucleotide context. We observed that mutations in contexts that deviate from the characteristic contexts around passenger mutations provide a signal in favor of driver genes. We therefore developed a method that combines this feature with the signals traditionally used for driver-gene identification. We applied our metho
SUBMITTER: Dietlein F
PROVIDER: S-EPMC7031046 | biostudies-literature | 2020 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA