LogoClawIndex
CasesSkillsAbout
LogoClawIndex

ClawIndex

OpenClaw Skills & Use Case Index

ClawIndex is an ecosystem-driven index of OpenClaw skills and real-world use cases.

Index

Skills·
Cases

Meta

About·
Disclaimer·
Email·
GitHub
© 2026 ClawIndex All Rights Reserved.

Skills tagged: NGS

Browse skills that share this tag.

  • multiqc-qc-reports - Multi-Sample QC Report Aggregator
    bioinformaticsquality controlreportingNGS

    ★ 1 · Updated 2026-06-30

    Aggregates QC outputs from 150+ bioinformatics tools into a single interactive HTML report

    ⚙ scan directories⚙ parse tool logs⚙ generate HTML report
  • pysam - Genomic Data Processing Toolkit
    bioinformaticsgenomicsNGSsequencing

    ★ 394 · 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
    bioinformaticsgenomicsNGSalignment

    ★ 2 · Updated 2026-06-15

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

    ⚙ Open alignment files⚙ Open variant files⚙ Open sequence files
  • pysam - Genomic Data File Processing
    genomicsbioinformaticsNGSsequence-processing

    ★ 4 · Updated 2026-06-15

    Read/write genomic files including SAM/BAM alignments, VCF variants, and FASTA/FASTQ sequences with Python interface to htslib.

    ⚙ read SAM/BAM/CRAM files⚙ write SAM/BAM/CRAM files⚙ read VCF/BCF files
  • pysam - Genomic file toolkit for NGS data
    bioinformaticsgenomicsNGSsequence analysis

    ★ 64 · 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

    ★ 53 · Updated 2026-06-15

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

    ⚙ read alignment files⚙ write alignment files⚙ read variant files
  • pysam - Genomic File Processing Toolkit
    genomicsbioinformaticsNGSsequencing

    ★ 359 · Updated 2026-06-15

    Read and write genomic alignment, variant, and sequence files for NGS data processing

    ⚙ read SAM/BAM/CRAM files⚙ read VCF/BCF files⚙ read FASTA/FASTQ files
  • genomics-pipelines - Genomics Analysis Pipeline Patterns
    genomicsbioinformaticspipelinesNGS

    ★ 15 · Updated 2026-02-12

    Patterns for building robust, reproducible genomics analysis pipelines

    ⚙ build analysis pipelines⚙ process NGS data⚙ call variants