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.
Source facts
- Repository
- x-cmd/skill
- Last source activity
- January 30, 2026 at 12:43
- Detected SKILL.md language
- English
- Stars
- 26
- Forks
- 5
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| name | pysam |
|---|---|
| description | Genomic file toolkit. Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences, extract regions, calculate coverage, for NGS data processing pipelines. |