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.
Installation and usage
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.
Depois de instalar, você pode usar esta skill executando o seguinte comando no terminal:
skills use bio-vcf