Versions
Description
CNVkit is a flexible toolkit for calling copy number from DNA sequencing data. For whole-exome and targeted gene panels, off-target sequencing reads from hybrid capture are used to improve copy number estimates. Targeted amplicon capture and whole-genome sequencing protocols are also supported. CNVKit implements a variety of visualization modes, analysis methods, and output file formats for easy integration into existing pipelines.
Repository
http://github.com/etal/cnvkit.git
Project Slug
cnvkit
Last Built
1 year ago failed
Maintainers
Home Page
http://github.com/etal/cnvkit.git
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Tags
bionformatics, ngs, sequencing
Short URLs
cnvkit.readthedocs.io
cnvkit.rtfd.io
Default Version
stable
'latest' Version
master