Skip to main content 홈 크리에이터 z43l zeus-agent bioinformatics
bioinformatics Gateway to 400+ bioinformatics skills from bioSkills and ClawBio. Covers genomics, transcriptomics, single-cell, variant calling, pharmacogenomics, metagenomics, structural biology, and more. Fetches domain-specific reference material on demand.
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Zip 다운로드 다운로드 중... Configure and use Honcho memory with Hermes -- cross-session user modeling, multi-profile peer isolation, observation config, dialectic reasoning, session summaries, and context budget enforcement. Use when setting up Honcho, troubleshooting memory, managing profiles with Honcho peers, or tuning observation, recall, and dialectic settings.
name bioinformatics description Gateway to 400+ bioinformatics skills from bioSkills and ClawBio. Covers genomics, transcriptomics, single-cell, variant calling, pharmacogenomics, metagenomics, structural biology, and more. Fetches domain-specific reference material on demand. version 1.0.0 platforms ["linux","macos"] metadata {"hermes":{"tags":["bioinformatics","genomics","sequencing","biology","research","science"],"category":"research"}}
Bioinformatics Skills Gateway
Use when asked about bioinformatics, genomics, sequencing, variant calling, gene expression, single-cell analysis, protein structure, pharmacogenomics, metagenomics, phylogenetics, or any computational biology task.
This skill is a gateway to two open-source bioinformatics skill libraries. Instead of bundling hundreds of domain-specific skills, it indexes them and fetches what you need on demand.
Sources
◆ bioSkills — 385 reference skills (code patterns, parameter guides, decision trees)
Repo: https://github.com/GPTomics/bioSkills
Format: SKILL.md per topic with code examples. Python/R/CLI.
◆ ClawBio — 33 runnable pipeline skills (executable scripts, reproducibility bundles)
Repo: https://github.com/ClawBio/ClawBio
Format: Python scripts with demos. Each analysis exports report.md + commands.sh + environment.yml.
How to fetch and use a skill
Identify the domain and skill name from the index below.
Clone the relevant repo (shallow clone to save time):
git clone --depth 1 https://github.com/GPTomics/bioSkills.git /tmp/bioSkills
git clone --depth 1 https://github.com/ClawBio/ClawBio.git /tmp/ClawBio
Read the specific skill:
cat /tmp/bioSkills/variant-calling/gatk-variant-calling/SKILL.md
cat /tmp/ClawBio/skills/pharmgx-reporter/README.md
Follow the fetched skill as reference material. These are NOT Zeus-format skills — treat them as expert domain guides. They contain correct parameters, proper tool flags, and validated pipelines.
Skill Index by Domain
Sequence Fundamentals bioSkills:
sequence-io/ — read-sequences, write-sequences, format-conversion, batch-processing, compressed-files, fastq-quality, filter-sequences, paired-end-fastq, sequence-statistics
sequence-manipulation/ — seq-objects, reverse-complement, transcription-translation, motif-search, codon-usage, sequence-properties, sequence-slicing
ClawBio:
seq-wrangler — Sequence QC, alignment, and BAM processing (wraps FastQC, BWA, SAMtools)
Read QC & Alignment bioSkills:
read-qc/ — quality-reports, fastp-workflow, adapter-trimming, quality-filtering, umi-processing, contamination-screening, rnaseq-qc
read-alignment/ — bwa-alignment, star-alignment, hisat2-alignment, bowtie2-alignment
alignment-files/ — sam-bam-basics, alignment-sorting, alignment-filtering, bam-statistics, duplicate-handling, pileup-generation
Variant Calling & Annotation bioSkills:
variant-calling/ — gatk-variant-calling, deepvariant, variant-calling (bcftools), joint-calling, structural-variant-calling, filtering-best-practices, variant-annotation, variant-normalization, vcf-basics, vcf-manipulation, vcf-statistics, consensus-sequences, clinical-interpretation
ClawBio:
vcf-annotator — VEP + ClinVar + gnomAD annotation with ancestry-aware context
variant-annotation — Variant annotation pipeline
Differential Expression (Bulk RNA-seq) bioSkills:
differential-expression/ — deseq2-basics, edger-basics, batch-correction, de-results, de-visualization, timeseries-de
rna-quantification/ — alignment-free-quant (Salmon/kallisto), featurecounts-counting, tximport-workflow, count-matrix-qc
expression-matrix/ — counts-ingest, gene-id-mapping, metadata-joins, sparse-handling
ClawBio:
rnaseq-de — Full DE pipeline with QC, normalization, and visualization
diff-visualizer — Rich visualization and reporting for DE results
Single-Cell RNA-seq bioSkills:
single-cell/ — preprocessing, clustering, batch-integration, cell-annotation, cell-communication, doublet-detection, markers-annotation, trajectory-inference, multimodal-integration, perturb-seq, scatac-analysis, lineage-tracing, metabolite-communication, data-io
ClawBio:
scrna-orchestrator — Full Scanpy pipeline (QC, clustering, markers, annotation)
scrna-embedding — scVI-based latent embedding and batch integration
Spatial Transcriptomics bioSkills:
spatial-transcriptomics/ — spatial-data-io, spatial-preprocessing, spatial-domains, spatial-deconvolution, spatial-communication, spatial-neighbors, spatial-statistics, spatial-visualization, spatial-multiomics, spatial-proteomics, image-analysis
Epigenomics bioSkills:
chip-seq/ — peak-calling, differential-binding, motif-analysis, peak-annotation, chipseq-qc, chipseq-visualization, super-enhancers
atac-seq/ — atac-peak-calling, atac-qc, differential-accessibility, footprinting, motif-deviation, nucleosome-positioning
methylation-analysis/ — bismark-alignment, methylation-calling, dmr-detection, methylkit-analysis
hi-c-analysis/ — hic-data-io, tad-detection, loop-calling, compartment-analysis, contact-pairs, matrix-operations, hic-visualization, hic-differential
ClawBio:
methylation-clock — Epigenetic age estimation
Pharmacogenomics & Clinical bioSkills:
clinical-databases/ — clinvar-lookup, gnomad-frequencies, dbsnp-queries, pharmacogenomics, polygenic-risk, hla-typing, variant-prioritization, somatic-signatures, tumor-mutational-burden, myvariant-queries
ClawBio:
pharmgx-reporter — PGx report from 23andMe/AncestryDNA (12 genes, 31 SNPs, 51 drugs)
drug-photo — Photo of medication → personalized PGx dosage card (via vision)
clinpgx — ClinPGx API for gene-drug data and CPIC guidelines
gwas-lookup — Federated variant lookup across 9 genomic databases
gwas-prs — Polygenic risk scores from consumer genetic data
nutrigx_advisor — Personalized nutrition from consumer genetic data
Population Genetics & GWAS bioSkills:
population-genetics/ — association-testing (PLINK GWAS), plink-basics, population-structure, linkage-disequilibrium, scikit-allel-analysis, selection-statistics
causal-genomics/ — mendelian-randomization, fine-mapping, colocalization-analysis, mediation-analysis, pleiotropy-detection
phasing-imputation/ — haplotype-phasing, genotype-imputation, imputation-qc, reference-panels
ClawBio:
claw-ancestry-pca — Ancestry PCA against SGDP reference panel
Metagenomics & Microbiome bioSkills:
metagenomics/ — kraken-classification, metaphlan-profiling, abundance-estimation, functional-profiling, amr-detection, strain-tracking, metagenome-visualization
microbiome/ — amplicon-processing, diversity-analysis, differential-abundance, taxonomy-assignment, functional-prediction, qiime2-workflow
ClawBio:
claw-metagenomics — Shotgun metagenomics profiling (taxonomy, resistome, functional pathways)
Genome Assembly & Annotation bioSkills:
genome-assembly/ — hifi-assembly, long-read-assembly, short-read-assembly, metagenome-assembly, assembly-polishing, assembly-qc, scaffolding, contamination-detection
genome-annotation/ — eukaryotic-gene-prediction, prokaryotic-annotation, functional-annotation, ncrna-annotation, repeat-annotation, annotation-transfer
long-read-sequencing/ — basecalling, long-read-alignment, long-read-qc, clair3-variants, structural-variants, medaka-polishing, nanopore-methylation, isoseq-analysis
Structural Biology & Chemoinformatics bioSkills:
structural-biology/ — alphafold-predictions, modern-structure-prediction, structure-io, structure-navigation, structure-modification, geometric-analysis
chemoinformatics/ — molecular-io, molecular-descriptors, similarity-searching, substructure-search, virtual-screening, admet-prediction, reaction-enumeration
ClawBio:
struct-predictor — Local AlphaFold/Boltz/Chai structure prediction with comparison
Proteomics bioSkills:
proteomics/ — data-import, peptide-identification, protein-inference, quantification, differential-abundance, dia-analysis, ptm-analysis, proteomics-qc, spectral-libraries
ClawBio:
proteomics-de — Proteomics differential expression
Pathway Analysis & Gene Networks bioSkills:
pathway-analysis/ — go-enrichment, gsea, kegg-pathways, reactome-pathways, wikipathways, enrichment-visualization
gene-regulatory-networks/ — scenic-regulons, coexpression-networks, differential-networks, multiomics-grn, perturbation-simulation
Immunoinformatics bioSkills:
immunoinformatics/ — mhc-binding-prediction, epitope-prediction, neoantigen-prediction, immunogenicity-scoring, tcr-epitope-binding
tcr-bcr-analysis/ — mixcr-analysis, scirpy-analysis, immcantation-analysis, repertoire-visualization, vdjtools-analysis
CRISPR & Genome Engineering bioSkills:
crispr-screens/ — mageck-analysis, jacks-analysis, hit-calling, screen-qc, library-design, crispresso-editing, base-editing-analysis, batch-correction
genome-engineering/ — grna-design, off-target-prediction, hdr-template-design, base-editing-design, prime-editing-design
Workflow Management bioSkills:
workflow-management/ — snakemake-workflows, nextflow-pipelines, cwl-workflows, wdl-workflows
ClawBio:
repro-enforcer — Export any analysis as reproducibility bundle (Conda env + Singularity + checksums)
galaxy-bridge — Access 8,000+ Galaxy tools from usegalaxy.org
Specialized Domains bioSkills:
alternative-splicing/ — splicing-quantification, differential-splicing, isoform-switching, sashimi-plots, single-cell-splicing, splicing-qc
ecological-genomics/ — edna-metabarcoding, landscape-genomics, conservation-genetics, biodiversity-metrics, community-ecology, species-delimitation
epidemiological-genomics/ — pathogen-typing, variant-surveillance, phylodynamics, transmission-inference, amr-surveillance
liquid-biopsy/ — cfdna-preprocessing, ctdna-mutation-detection, fragment-analysis, tumor-fraction-estimation, methylation-based-detection, longitudinal-monitoring
epitranscriptomics/ — m6a-peak-calling, m6a-differential, m6anet-analysis, merip-preprocessing, modification-visualization
metabolomics/ — xcms-preprocessing, metabolite-annotation, normalization-qc, statistical-analysis, pathway-mapping, lipidomics, targeted-analysis, msdial-preprocessing
flow-cytometry/ — fcs-handling, gating-analysis, compensation-transformation, clustering-phenotyping, differential-analysis, cytometry-qc, doublet-detection, bead-normalization
systems-biology/ — flux-balance-analysis, metabolic-reconstruction, gene-essentiality, context-specific-models, model-curation
rna-structure/ — secondary-structure-prediction, ncrna-search, structure-probing
Data Visualization & Reporting bioSkills:
data-visualization/ — ggplot2-fundamentals, heatmaps-clustering, volcano-customization, circos-plots, genome-browser-tracks, interactive-visualization, multipanel-figures, network-visualization, upset-plots, color-palettes, specialized-omics-plots, genome-tracks
reporting/ — rmarkdown-reports, quarto-reports, jupyter-reports, automated-qc-reports, figure-export
ClawBio:
profile-report — Analysis profile reporting
data-extractor — Extract numerical data from scientific figure images (via vision)
lit-synthesizer — PubMed/bioRxiv search, summarization, citation graphs
pubmed-summariser — Gene/disease PubMed search with structured briefing
Database Access bioSkills:
database-access/ — entrez-search, entrez-fetch, entrez-link, blast-searches, local-blast, sra-data, geo-data, uniprot-access, batch-downloads, interaction-databases, sequence-similarity
ClawBio:
ukb-navigator — Semantic search across 12,000+ UK Biobank fields
clinical-trial-finder — Clinical trial discovery
Experimental Design bioSkills:
experimental-design/ — power-analysis, sample-size, batch-design, multiple-testing
Machine Learning for Omics bioSkills:
machine-learning/ — omics-classifiers, biomarker-discovery, survival-analysis, model-validation, prediction-explanation, atlas-mapping
ClawBio:
claw-semantic-sim — Semantic similarity index for disease literature (PubMedBERT)
omics-target-evidence-mapper — Aggregate target-level evidence across omics sources
Environment Setup These skills assume a bioinformatics workstation. Common dependencies:
pip install biopython pysam cyvcf2 pybedtools pyBigWig scikit-allel anndata scanpy mygene
Rscript -e 'BiocManager::install(c("DESeq2","edgeR","Seurat","clusterProfiler","methylKit"))'
sudo apt install samtools bcftools ncbi-blast+ minimap2 bedtools
brew install samtools bcftools blast minimap2 bedtools
conda install -c bioconda samtools bcftools blast minimap2 bedtools fastp kraken2
Pitfalls
The fetched skills are NOT in Zeus SKILL.md format. They use their own structure (bioSkills: code pattern cookbooks; ClawBio: README + Python scripts). Read them as expert reference material.
bioSkills are reference guides — they show correct parameters and code patterns but aren't executable pipelines.
ClawBio skills are executable — many have --demo flags and can be run directly.
Both repos assume bioinformatics tools are installed. Check prerequisites before running pipelines.
For ClawBio, run pip install -r requirements.txt in the cloned repo first.
Genomic data files can be very large. Be mindful of disk space when downloading reference genomes, SRA datasets, or building indices.