pysam
About
Pysam provides a Pythonic interface to htslib for reading and writing genomic file formats like SAM/BAM/CRAM, VCF/BCF, and FASTA/FASTQ. Use it in NGS pipelines to extract regions, calculate coverage, perform pileup analysis, and execute samtools-like commands. It's essential for developers building bioinformatics workflows involving alignment, variant calling, or sequence data processing.
Quick Install
Claude Code
Recommendednpx skills add aiskillstore/marketplace -a claude-code/plugin add https://github.com/aiskillstore/marketplacegit clone https://github.com/aiskillstore/marketplace.git ~/.claude/skills/pysamCopy and paste this command in Claude Code to install this skill
GitHub Repository
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