★ 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 produce this output.
★ 4 · Updated 2026-06-15
Read/write genomic files including SAM/BAM alignments, VCF variants, and FASTA/FASTQ sequences with Python interface to htslib.
★ 64 · Updated 2026-06-15
Read and write genomic files including SAM/BAM/CRAM alignments, VCF/BCF variants, and FASTA/FASTQ sequences
★ 53 · Updated 2026-06-15
Read/write genomic files, query regions, calculate coverage for NGS data
★ 359 · Updated 2026-06-15
Read and write genomic alignment, variant, and sequence files for NGS data processing
★ 7 · Updated 2026-02-13
Navigate between Jekyll plugins and their tests
★ 602 · Updated 2026-02-13
Tooling for finding coverage gaps, parsing coverage files, and handling exclusion markers