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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."
Source: github.com/davila7/claude-code-templates/tree/main/cli-tool/components/skills/scientific/pysam · License: MIT
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