bio-clinical-databases-hla-typing
OfficialFast HLA typing from NGS data.
Authorstellaromics
Version1.0.0
Installs0
System Documentation
What problem does it solve?
HLA typing from NGS data is essential for transplant matching and pharmacogenomic screening, but many clinicians and researchers lack integrated workflows to call and interpret HLA alleles across data types.
Core Features & Use Cases
- End-to-end HLA typing: call HLA-A, HLA-B, HLA-C (and optionally Class II loci with other tools) from WES/WGS or RNA-seq data.
- Tool-agnostic parsing: parse OptiType, HLA-HD, or arcasHLA outputs into standardized four-field alleles.
- Use Case: A transplant team can quickly generate a report showing patient HLA alleles for matching and drug-response screening.
Quick Start
Run OptiType on a WES or RNA-seq dataset to obtain four-field HLA-A, B, and C calls.
Dependency Matrix
Required Modules
None requiredComponents
Standard package💻 Claude Code Installation
Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.
Please help me install this Skill: Name: bio-clinical-databases-hla-typing Download link: https://github.com/stellaromics/fast-bioinfo/archive/main.zip#bio-clinical-databases-hla-typing Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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