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
Actualizado 3/8/2026
Estrellas
1987
Forks
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.
Instalación
$ install --globalskills.sh
Uso
Después de instalarlo, puedes usar este skill ejecutando el siguiente comando en tu terminal:
skills use bio-copy-number-cnvkit-analysis