Revision 03858a79084515eb808bb3275cb2078a4dde3909

Package: cnvkit @ 0.9.5

Synopsis

Copy number variant detection from targeted DNA sequencing

Description

CNVkit is a Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina and Ion Torrent.

Home page

https://cnvkit.readthedocs.org/

Location

gnu/packages/bioinformatics.scm (line: 13041, column: 2)

License

• ASL 2.0

Derivations

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