ActiveDriverWGS

MaRDI QIDQ97814CRANFDO

Authors Juri Reimand, Helen Zhu

Last update 13 March 2026

Copyright license GNU General Public License, version 3.0

Software version identifier 1.0.1, 1.1.0, 1.1.1, 1.1.2, 1.2.0, PACKAGES.rds, 1.2.1

Description

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.

Cites work

• Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks

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