From the author
Genomic file toolkit. Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences, extract regions, calculate coverage, for NGS data processing pipelines.
Install
npx skills add BioTender-max/awesome-bio-agent-skills --skill pysam -a claude-code
Installs to .claude/skills/pysam/ · Each command fetches the skill straight from GitHub with the open skills CLI.
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