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
अपडेट किया गया 3/8/2026
स्टार
1987
फोर्क
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.
इंस्टॉलेशन
$ install --globalskills.sh
उपयोग
इंस्टॉल करने के बाद, आप टर्मिनल में यह कमांड चलाकर इस स्किल का उपयोग कर सकते हैं:
skills use bio-copy-number-cnvkit-analysis