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
اپ ڈیٹ ہوا 3/8/2026
اسٹارز
1987
فورکس
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.
انسٹالیشن
$ install --globalskills.sh
استعمال
انسٹال کرنے کے بعد، آپ یہ اسکل ٹرمینل میں درج ذیل کمانڈ چلا کر استعمال کر سکتے ہیں:
skills use bio-copy-number-cnvkit-analysis