pysam
K-Dense-AI/claude-scientific-skills
28,042Added Jun 5, 2026
genomicsbam-samvcfngssequence-alignmentbioinformaticsvariant-calling
Summary
Genomic file toolkit. Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences, extract regions, calculate coverage, for NGS data processing pipelines.