pysam
About
Genomic file toolkit. Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences, extract regions, calculate coverage, for NGS data processing pipelines.
Quick Install
/plugin add https://github.com/K-Dense-AI/claude-scientific-skills/tree/main/pysamCopy and paste this command in Claude Code to install this skill
GitHub 仓库
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