pysam
Genomic file toolkit. Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences, extract regions, calculate coverage, for NGS data processing pipelines.
Also installable via skills CLI
npx skills add overtimepog/AgentTheo/.claude/skills/scientific-skills/pysam
Source
Path:
.claude/skills/scientific-skills/pysam/SKILL.md(main)