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. |
hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/cnvkit_batch
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
Run the CNVkit pipeline on one or more BAM files | 0.9.11+galaxy1 | 21.05 |