| 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://radegast.galaxyproject.org/repos/iuc/cnvkit_autobin
| Name | Description | Version | Minimum Galaxy Version |
|---|---|---|---|
| Estimates read counts or depths in a BAM file | 0.9.12+galaxy0 | 21.05 | |