A Driver Discovery Tool for Cancer Whole Genomes R package ActiveDriverWGS version 1.2.1 A method for finding enrichments of somatic single nucleotide variants (SNVs) and small insertions-deletions (Indels) in functional elements in the human genome. 'ActiveDriverWGS' detects coding and noncoding cancer driver elements using whole genome sequencing data. The method is part of the publication H. Zhu et al. (2020) <doi:10.1016/j.molcel.2019.12.027> "Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks" in Molecular Cell. Software Depends: R (>= 3.5) Imports: BSgenome, Biostrings, GenomeInfoDb, GenomicRanges, IRanges, S4Vectors Suggests: BSgenome.Hsapiens.UCSC.hg19, BSgenome.Hsapiens.UCSC.hg38, BSgenome.Mmusculus.UCSC.mm9, BSgenome.Mmusculus.UCSC.mm10, knitr, testthat, rmarkdown Juri Reimand <juri.reimand@utoronto.ca> Comprehensive R Archive Network (CRAN) Juri Reimand [aut, cre], Helen Zhu [ctb], Kevin Cheng [ctb] GPL-3 2026-03-13 application/tgz https://CRAN.R-project.org/package=ActiveDriverWGS doi:10.32614/CRAN.package.ActiveDriverWGS