home/categories/bioinformatics/freedomintelligence-openclaw-medical-skills-skills-bio-copy-number-cnvkit-analysis-skill-md
bioinformaticsresearch
bio-copy-number-cnvkit-analysis
Detect copy number variants from targeted/exome sequencing using CNVkit. Supports tumor-normal pairs, tumor-only, and germline CNV calling. Use when detecting CNVs from WES or targeted panel sequencing data.
maintainer
FreedomIntelligence
更新于 3/8/2026
星标
1987
分支
270
quick start
Installation and usage
Detect copy number variants from targeted/exome sequencing using CNVkit. Supports tumor-normal pairs, tumor-only, and germline CNV calling. Use when detecting CNVs from WES or targeted panel sequencing data.
安装
$ install --globalskills.sh
使用
安装后,您可以通过在终端运行以下命令来使用此技能:
skills use bio-copy-number-cnvkit-analysis