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# CITATION file created with {cffr} R package
# See also: https://docs.ropensci.org/cffr/
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cff-version: 1.2.0
message: 'To cite package "ActiveDriverWGS" in publications use:'
type: software
license: GPL-3.0-only
title: 'ActiveDriverWGS: A Driver Discovery Tool for Cancer Whole Genomes'
version: 1.2.1
doi: 10.32614/CRAN.package.ActiveDriverWGS
abstract: 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)
  <https://doi.org/10.1016/j.molcel.2019.12.027> "Candidate Cancer Driver Mutations
  in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks" in
  Molecular Cell.
authors:
- family-names: Reimand
  given-names: Juri
  email: juri.reimand@utoronto.ca
repository: https://reimand0.r-universe.dev
commit: c53bb4f6864695fb5856b3e8fd349835b1b9d2ae
date-released: '2026-03-13'
contact:
- family-names: Reimand
  given-names: Juri
  email: juri.reimand@utoronto.ca