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.

by davila7· Repository·testing
Run in AgentAreaBrowse All Skills
Also installable via skills CLI
npx skills add davila7/claude-code-templates/cli-tool/components/skills/scientific/pysam

Source

Repo:SkillsMP + GitHub Raw
Path:cli-tool/components/skills/scientific/pysam(main)

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