cnvkit 0.9.5 Copy number variant detection from targeted DNA sequencing
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.
- Website: https://cnvkit.readthedocs.org/
- License: ASL 2.0
- Package source: bioinformatics.scm
- Patches: None
- Builds: x86_64-linux, i686-linux