bio-copy-number-cnvkit-analysis
0
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.
Install this skill
Run this command in your terminal. No account required — it auto-detects your AI tool and installs the skill file.
npx @skills-hub-ai/cli install openclaw-medical-bio-copy-number-cnvkit-analysisOr download directly:
View all CLI commands →Setup by platform
Instructions
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