bioinformatics – skill Dữ liệu & Khoa học cho agent AI
Cổng vào hơn 400 kỹ năng về gene học và sinh học tính toán.
Cài skill bioinformatics bằng một lệnh
Chọn công cụ bạn đang dùng, copy lệnh và dán vào terminal. Skill sẽ nằm trong thư mục skills của công cụ đó và sẵn sàng dùng ở phiên làm việc tiếp theo.
Claude Code
mkdir -p ~/.claude/skills && curl -fsSL https://skill.dn1nguoi.com/z/bioinformatics-df050.tgz | tar xz -C ~/.claude/skills
Gọi trong Claude Code: /bioinformatics – rồi mô tả công việc bạn muốn làm.
Codex
mkdir -p ~/.codex/skills && curl -fsSL https://skill.dn1nguoi.com/z/bioinformatics-df050.tgz | tar xz -C ~/.codex/skills
Gọi trong Codex: $bioinformatics – rồi mô tả công việc bạn muốn làm.
Hermes Agent
mkdir -p ~/.hermes/skills && curl -fsSL https://skill.dn1nguoi.com/z/bioinformatics-df050.tgz | tar xz -C ~/.hermes/skills
Gọi trong Hermes Agent: /bioinformatics – rồi mô tả công việc bạn muốn làm.
DeepSeek
mkdir -p ~/.deepcode/skills && curl -fsSL https://skill.dn1nguoi.com/z/bioinformatics-df050.tgz | tar xz -C ~/.deepcode/skills
Gọi trong DeepSeek: /bioinformatics – rồi mô tả công việc bạn muốn làm.
Nội dung SKILL.md
Nội dung SKILL.md gốc bằng tiếng Anh.
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
1. Identify the domain and skill name from the index below.
2. Clone the relevant repo (shallow clone to save time):
# bioSkills (reference material)
git clone --depth 1 https://github.com/GPTomics/bioSkills.git ~/.hermes/cache/scratch/bioSkills
# ClawBio (runnable pipelines)
git clone --depth 1 https://github.com/ClawBio/ClawBio.git ~/.hermes/cache/scratch/ClawBio
3. Read the specific skill:
# bioSkills — each skill is at: <category>/<skill-name>/SKILL.md
cat ~/.hermes/cache/scratch/bioSkills/variant-calling/gatk-variant-calling/SKILL.md
# ClawBio — each skill is at: skills/<skill-name>/
cat ~/.hermes/cache/scratch/ClawBio/skills/pharmgx-reporter/README.md
4. Follow the fetched skill as reference material. These are NOT Hermes-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-work
… (nội dung đầy đủ có trong gói tải về)
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