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.
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Skill Details
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Created
Jan 2026
Last Updated
5个月前
tools
tools bioinformatics
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