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Published January 30, 2018 | Version 1.13.0-rc1
Software Open

cancerit/CaVEMan: Release candidate - Overlapping reads

Authors/Creators

  • 1. Cancer Genome Project, Wellcome Trust Sanger Institute
  • 2. Cancer Genome Project, Wellcome Trust, Sanger Institute

Description

SNV expectation maximisation based mutation calling algorithm aimed at detecting somatic mutations in paired (tumour/normal) cancer samples. Supports both bam and cram format via htslib

Files

cancerit/CaVEMan-1.13.0-rc1.zip

Files (9.6 MB)

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md5:fc230f34057f20ad5e617931d51cb905
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Additional details

Related works

Is supplement to
https://github.com/cancerit/CaVEMan/tree/1.13.0-rc1 (URL)