Data Science & Analytics
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.
- Publisher / source
- davila7/claude-code-templates (found on skills.sh)
- Upstream record
- davila7/claude-code-templates
- Version
- Version 2
- Published
- Publication review
- Approved for publication
- Content fingerprint
fb020d09b420ee59eead6780e6ce81d1b2236194ccc3063088ca53f2b7ae7153