★ 4 · Updated 2026-06-15
Read/write genomic files including SAM/BAM alignments, VCF variants, and FASTA/FASTQ sequences with Python interface to htslib.
Browse skills that share this capability.
★ 4 · Updated 2026-06-15
Read/write genomic files including SAM/BAM alignments, VCF variants, and FASTA/FASTQ sequences with Python interface to htslib.
★ 359 · Updated 2026-06-15
Read and write genomic alignment, variant, and sequence files for NGS data processing