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_antitarget
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
lists the chromosomal coordinates for targeted resequencing | 0.9.10+galaxy0 | 21.05 |