GPTomics/clawhub-installer
clawhub-installer/SKILL.md
Installs 425 bioinformatics skills covering sequence analysis, RNA-seq, single-cell, variant calling, metagenomics, structural biology, and 56 more categories. Use when setting up bioinformatics capabilities or when a bioinformatics task requires specialized skills not yet installed.
$ install --global
skillsauthnpx skillsauth add GPTomics/bioSkills clawhub-installerInstall this skill globally with one command. Works with Claude Code, Cursor, and Windsurf.
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SKILL.md
- name:
- clawhub-installer
- description:
- Installs 425 bioinformatics skills covering sequence analysis, RNA-seq, single-cell, variant calling, metagenomics, structural biology, and 56 more categories. Use when setting up bioinformatics capabilities or when a bioinformatics task requires specialized skills not yet installed.
- metadata:
- {"openclaw":{"requires":{"bins":["git"],"anyBins":["python3","Rscript"]},"os":["darwin","linux"],"emoji":"🧬"}}
bioSkills Installer
Meta-skill that installs the full bioSkills collection (425 skills across 62 categories) for bioinformatics analysis.
Installation
Run the bundled install script to download and install all bioSkills:
bash scripts/install-bioskills.sh
Or install only specific categories:
bash scripts/install-bioskills.sh --categories "single-cell,variant-calling,differential-expression"
What Gets Installed
425 skills across 62 categories covering:
- Sequence & Alignment (40): sequence-io, sequence-manipulation, alignment, alignment-files, database-access
- Read Processing (11): read-qc, read-alignment
- RNA-seq & Expression (14): differential-expression, rna-quantification, expression-matrix
- Single-Cell & Spatial (25): single-cell, spatial-transcriptomics
- Variant Analysis (21): variant-calling, copy-number, phasing-imputation
- Epigenomics (25): chip-seq, atac-seq, methylation-analysis, hi-c-analysis
- Metagenomics & Microbiome (13): metagenomics, microbiome
- Genomics & Assembly (29): genome-assembly, genome-annotation, genome-intervals, genome-engineering, primer-design
- Regulatory & Causal (13): gene-regulatory-networks, causal-genomics, rna-structure
- Temporal & Ecological (11): temporal-genomics, ecological-genomics
- Immunology & Clinical (25): immunoinformatics, clinical-databases, tcr-bcr-analysis, epidemiological-genomics
- Specialized Omics (36): proteomics, metabolomics, alternative-splicing, chemoinformatics, liquid-biopsy
- RNA Biology (20): small-rna-seq, epitranscriptomics, clip-seq, ribo-seq
- Phylogenetics & Evolution (16): phylogenetics, population-genetics, comparative-genomics
- Structural & Systems (11): structural-biology, systems-biology
- Screens & Cytometry (22): crispr-screens, flow-cytometry, imaging-mass-cytometry
- Pathway & Integration (14): pathway-analysis, multi-omics-integration, restriction-analysis
- Infrastructure (39): data-visualization, machine-learning, workflow-management, reporting, experimental-design, long-read-sequencing
- Workflows (40): end-to-end pipelines (FASTQ to results)
After Installation
Once installed, skills are automatically triggered based on the task at hand. Example requests:
- "I have RNA-seq counts from treated vs control samples - find the differentially expressed genes"
- "Call variants from this whole genome sequencing BAM file"
- "Cluster my single-cell RNA-seq data and find marker genes"
- "Predict the structure of this protein sequence"
- "Run a metagenomics classification on these shotgun reads"
Source
GitHub: https://github.com/GPTomics/bioSkills
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Create and manipulate Seq, MutableSeq, and SeqRecord objects using Biopython. Use when creating sequences from strings, modifying sequence data in-place, building annotated records for file output, or debugging post-1.78 Bio.Alphabet and immutability errors.
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