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OpenClaw Skills & Use Case Index

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Skills with capability: read variant files

Browse skills that share this capability.

  • pysam - Genomic Data Processing Toolkit
    bioinformaticsgenomicsNGSsequencing

    ★ 119 · Updated 2026-06-15

    Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences for NGS pipelines

    ⚙ read alignment files⚙ write alignment files⚙ fetch genomic regions
  • pysam - Genomic file toolkit for NGS data
    bioinformaticsgenomicsNGSsequence analysis

    ★ 6 · Updated 2026-06-15

    Read and write genomic files including SAM/BAM/CRAM alignments, VCF/BCF variants, and FASTA/FASTQ sequences

    ⚙ read alignment files⚙ read variant files⚙ read sequence files
  • pysam - Genomic file processing toolkit
    bioinformaticsgenomicssequencingNGS

    ★ 20 · Updated 2026-06-15

    Read/write genomic files, query regions, calculate coverage for NGS data

    ⚙ read alignment files⚙ write alignment files⚙ read variant files