pysam
About
Pysam is a Python toolkit for reading, writing, and analyzing common genomic file formats like SAM/BAM, VCF, and FASTA. It provides essential functionality for NGS pipelines, including region extraction, coverage calculation, and variant processing. Use this skill when building bioinformatics workflows that require direct manipulation of sequencing data and alignment files.
Quick Install
Claude Code
Recommendednpx skills add BbgnsurfTech/claude-skills-collection -a claude-code/plugin add https://github.com/BbgnsurfTech/claude-skills-collectiongit clone https://github.com/BbgnsurfTech/claude-skills-collection.git ~/.claude/skills/pysamCopy and paste this command in Claude Code to install this skill
GitHub Repository
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