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bio-vcf

This skill should be used when the user asks to analyze, filter, or inspect VCF/BCF variant files from WGS/WES sequencing. Triggers include requests to calculate variant statistics, filter variants by quality/depth/frequency, extract variants from specific chromosomes or regions, or export variant data as JSON for downstream analysis.

$ Installieren

git clone https://github.com/dakesan/cc-dnawork-plugin /tmp/cc-dnawork-plugin && cp -r /tmp/cc-dnawork-plugin/scientific-skills/vcf-toolkit ~/.claude/skills/cc-dnawork-plugin

// tip: Run this command in your terminal to install the skill