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.
- Industry
- writing
- License
- Unverified
- Source repo
- K-Dense-AI/scientific-agent-skills · ★ 30,891
- Source file
- skills/pysam/SKILL.md
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