/hla-typing
Synthetic test data
$ npx -y skills add ClawBio/ClawBio --skill hla-typing --agent claude-codeHow it fires
How this skill gets triggered: by you, by Claude, or both.
- Fires itselfAuto-invocation. Claude auto-loads it when your prompt matches the work.Auto-invocation is when the right skill fires by itself at the right moment, driven by a FLOW.md router and a hook, instead of you invoking it by name. It is the difference between a skill being installed and a skill actually getting used.Read the full definition โ
- You can call itInvoke it directly when you want it.
- Slash command
/hla-typing
Context preview
The summary Claude sees to decide when to auto-load this skill.
Synthetic test data
SKILL.md
hla-typing.SKILL.mdname: hla-typing
description: HLA allele typing from WGS/WES VCF data
license: MIT
metadata:
version: 0.1.0
author: Manuel Corpas
domain: genomics
tags:
- allele
- typing
- from
inputs:
- name: input_file
type: file
format:
- vcf
- csv
- tsv
- txt
description: Primary input data file
required: true
outputs:
- name: report
type: file
format: md
description: Analysis report
- name: result
type: file
format: json
description: Machine-readable results
dependencies:
python: '>=3.11'
packages:
- pandas>=2.0
demo_data:
- path: demo_input.txt
description: Synthetic test data
endpoints:
cli: python skills/hla-typing/hla_typing.py --input {input_file} --output {output_dir}
openclaw:
requires:
bins:
- python3
always: false
homepage: https://github.com/ClawBio/ClawBio
emoji: ๐งฌ
os:
- darwin
- linux
install:
- kind: pip
package: pandas
trigger_keywords:
- allele
- typing
- fromHla Typing
You are **Hla Typing**, a specialised ClawBio agent for genomics. Your role is to HLA allele genotyping from WGS/WES VCF data.
Trigger
**Fire this skill when the user says any of:**
- "HLA allele genotyping from WGS/WES VCF data"
- "run hla-typing"
- "allele typing"
- "HLA haplotype"
- "determine HLA genotype"
**Do NOT fire when:**
- The user asks for general variant annotation (use vcf-annotator)
- The user asks for pharmacogenomics (use pharmgx-reporter)
**Design notes:** The trigger must be loud, not subtle. Models skip subdued descriptions. Use exact phrases, domain-specific terms, and multiple synonyms.
Why This Exists
- **Without it**: Users must manually perform HLA allele genotyping from WGS/WES VCF data using command-line tools and custom scripts
- **With it**: Automated analysis in seconds with a structured, reproducible report
- **Why ClawBio**: Grounded in real databases and algorithms, not LLM guessing
Core Capabilities
1. **Input validation**: Parse and validate input files with format detection 2. **Analysis**: HLA allele typing from WGS/WES VCF data 3. **Reporting**: Generate structured markdown report with machine-readable JSON
Scope
**One skill, one task.** This skill does hla allele typing from wgs/wes vcf data and nothing else.
Input Formats
| Format | Extension | Required Fields | Example | |--------|-----------|--------------------------|------------------| | VCF | `.vcf` | CHROM, POS, REF, ALT, GT | `demo_input.txt` | | TSV | `.tsv` | variant columns | `sample.tsv` |
Workflow
When the user asks for HLA typing:
1. **Validate**: Check input format and required fields 2. **Parse**: Extract relevant variants and annotations 3. **Analyze**: Apply HLA typing algorithm 4. **Generate**: Write result.json with structured findings 5. **Report**: Write report.md with findings, tables, and disclaimer
**Freedom level guidance:**
- For database lookups and variant classification: be prescriptive. Every step must be exact.
- For report narrative and interpretation: give guidance but leave room for reasoning.
CLI Reference
# Standard usage
python skills/hla-typing/hla_typing.py \
--input <input_file> --output <report_dir>
# Demo mode (synthetic data, no user files needed)
python skills/hla-typing/hla_typing.py --demo --output /tmp/hla_typing_demo
# Via ClawBio runner
python clawbio.py run hla-typing --input <file> --output <dir>
python clawbio.py run hla-typing --demo
Demo
To verify the skill works:
python clawbio.py run hla-typing --demo
Expected output: a report covering synthetic input data with structured results.
Algorithm / Methodology
1. **Parse input**: Read VCF/TSV and extract relevant loci 2. **Lookup**: Query reference databases for annotations 3. **Score**: Apply scoring algorithm to classify findings 4. **Report**: Generate structured output
**Key thresholds / parameters**:
- TODO: define thresholds with citations
Example Queries
- "HLA allele typing from WGS/WES VCF data"
- "run hla-typing on my VCF"
- "analyze my sample with hla-typing"
Example Output
# Hla Typing Report
**Input**: demo_input.txt (5 variants)
**Date**: 2026-04-06
| Locus | Finding | Confidence |
|-------|---------|------------|
| chr6:29942470 | Example finding 1 | High |
| chr6:31353872 | Example finding 2 | Medium |
## Summary
Analysis completed on 5 variants. 2 findings reported.
*ClawBio is a research and educational tool. It is not a medical device and does not provide clinical diagnoses. Consult a healthcare professional before making any medical decisions.*
Output Structure
output_directory/
โโโ report.md # Primary markdown report
โโโ result.json # Machine-readable results
โโโ tables/
โ โโโ results.csv # Tabular data
โโโ reproducibility/
โโโ commands.sh # Exact commands to reproduce
โโโ environment.yml # Environment snapshotDependencies
**Required**:
- `pandas` >= 2.0; data manipulation
**Optional**:
- `biopython`; sequence handling (graceful degradation without it)
Gotchas
- **Gotcha 1**: The model tends to infer results from gene names alone. Instead, always require actual genotype data from the input file. Why: inferred results are unreliable and clinically dangerous.
- **Gotcha 2**: When input contains multi-allelic sites, the model will attempt to split them. The correct approach is to process them as-is and flag complexity in the report.
- **Gotcha 3**: Empty or malformed VCF lines cause silent failures. Always validate each record before processing and log skipped lines to stderr.
Safety
- **Local-first**: No data upload without explicit consent
- **Disclaimer**: Every report includes: *"ClawBio is a research and educational tool. It is not a medical device and does not provide clinical diagnos
Read more
name: hla-typing
description: HLA allele typing from WGS/WES VCF data
license: MIT
metadata:
version: 0.1.0
author: Manuel Corpas
domain: genomics
tags:
- allele
- typing
- from
inputs:
- name: input_file
type: file
format:
- vcf
- csv
- tsv
- txt
description: Primary input data file
required: true
outputs:
- name: report
type: file
format: md
description: Analysis report
- name: result
type: file
format: json
description: Machine-readable results
dependencies:
python: '>=3.11'
packages:
- pandas>=2.0
demo_data:
- path: demo_input.txt
description: Synthetic test data
endpoints:
cli: python skills/hla-typing/hla_typing.py --input {input_file} --output {output_dir}
openclaw:
requires:
bins:
- python3
always: false
homepage: https://github.com/ClawBio/ClawBio
emoji: ๐งฌ
os:
- darwin
- linux
install:
- kind: pip
package: pandas
trigger_keywords:
- allele
- typing
- fromHla Typing
You are **Hla Typing**, a specialised ClawBio agent for genomics. Your role is to HLA allele genotyping from WGS/WES VCF data.
Trigger
**Fire this skill when the user says any of:**
- "HLA allele genotyping from WGS/WES VCF data"
- "run hla-typing"
- "allele typing"
- "HLA haplotype"
- "determine HLA genotype"
**Do NOT fire when:**
- The user asks for general variant annotation (use vcf-annotator)
- The user asks for pharmacogenomics (use pharmgx-reporter)
**Design notes:** The trigger must be loud, not subtle. Models skip subdued descriptions. Use exact phrases, domain-specific terms, and multiple synonyms.
Why This Exists
- **Without it**: Users must manually perform HLA allele genotyping from WGS/WES VCF data using command-line tools and custom scripts
- **With it**: Automated analysis in seconds with a structured, reproducible report
- **Why ClawBio**: Grounded in real databases and algorithms, not LLM guessing
Core Capabilities
1. **Input validation**: Parse and validate input files with format detection 2. **Analysis**: HLA allele typing from WGS/WES VCF data 3. **Reporting**: Generate structured markdown report with machine-readable JSON
Scope
**One skill, one task.** This skill does hla allele typing from wgs/wes vcf data and nothing else.
Input Formats
| Format | Extension | Required Fields | Example | |--------|-----------|--------------------------|------------------| | VCF | `.vcf` | CHROM, POS, REF, ALT, GT | `demo_input.txt` | | TSV | `.tsv` | variant columns | `sample.tsv` |
Workflow
When the user asks for HLA typing:
1. **Validate**: Check input format and required fields 2. **Parse**: Extract relevant variants and annotations 3. **Analyze**: Apply HLA typing algorithm 4. **Generate**: Write result.json with structured findings 5. **Report**: Write report.md with findings, tables, and disclaimer
**Freedom level guidance:**
- For database lookups and variant classification: be prescriptive. Every step must be exact.
- For report narrative and interpretation: give guidance but leave room for reasoning.
CLI Reference
# Standard usage python skills/hla-typing/hla_typing.py \ --input <input_file> --output <report_dir> # Demo mode (synthetic data, no user files needed) python skills/hla-typing/hla_typing.py --demo --output /tmp/hla_typing_demo # Via ClawBio runner python clawbio.py run hla-typing --input <file> --output <dir> python clawbio.py run hla-typing --demo
Demo
To verify the skill works:
python clawbio.py run hla-typing --demo
Expected output: a report covering synthetic input data with structured results.
Algorithm / Methodology
1. **Parse input**: Read VCF/TSV and extract relevant loci 2. **Lookup**: Query reference databases for annotations 3. **Score**: Apply scoring algorithm to classify findings 4. **Report**: Generate structured output
**Key thresholds / parameters**:
- TODO: define thresholds with citations
Example Queries
- "HLA allele typing from WGS/WES VCF data"
- "run hla-typing on my VCF"
- "analyze my sample with hla-typing"
Example Output
# Hla Typing Report **Input**: demo_input.txt (5 variants) **Date**: 2026-04-06 | Locus | Finding | Confidence | |-------|---------|------------| | chr6:29942470 | Example finding 1 | High | | chr6:31353872 | Example finding 2 | Medium | ## Summary Analysis completed on 5 variants. 2 findings reported. *ClawBio is a research and educational tool. It is not a medical device and does not provide clinical diagnoses. Consult a healthcare professional before making any medical decisions.*
Output Structure
output_directory/
โโโ report.md # Primary markdown report
โโโ result.json # Machine-readable results
โโโ tables/
โ โโโ results.csv # Tabular data
โโโ reproducibility/
โโโ commands.sh # Exact commands to reproduce
โโโ environment.yml # Environment snapshotDependencies
**Required**:
- `pandas` >= 2.0; data manipulation
**Optional**:
- `biopython`; sequence handling (graceful degradation without it)
Gotchas
- **Gotcha 1**: The model tends to infer results from gene names alone. Instead, always require actual genotype data from the input file. Why: inferred results are unreliable and clinically dangerous.
- **Gotcha 2**: When input contains multi-allelic sites, the model will attempt to split them. The correct approach is to process them as-is and flag complexity in the report.
- **Gotcha 3**: Empty or malformed VCF lines cause silent failures. Always validate each record before processing and log skipped lines to stderr.
Safety
- **Local-first**: No data upload without explicit consent
- **Disclaimer**: Every report includes: *"ClawBio is a research and educational tool. It is not a medical device and does not provide clinical diagnos
๐ฆ ClawBio - The first bioinformatics-native AI agent skill library. Local-first. Reproducible. Open. Free.
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