ActiveDriverWGS (Q97814)

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A Driver Discovery Tool for Cancer Whole Genomes
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    ActiveDriverWGS
    A Driver Discovery Tool for Cancer Whole Genomes

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      1.0.1
      22 March 2019
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      1.1.0
      7 September 2020
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      1.1.1
      17 September 2020
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      1.1.2
      30 November 2021
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      1.2.0
      3 September 2022
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      PACKAGES.rds
      9 July 2026
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      1.2.1
      13 March 2026
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      Helen Zhu
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      13 March 2026
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      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.
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