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clinpgx-database

Query ClinPGx REST endpoints for gene-drug interactions, CPIC guidelines, and allele data.

16|7|Updated Nov 20, 2025
Search Tags:#clinical-annotations#drug-labels#precision-medicine#pharmacogenomics#alleles#CPIC
One-click install
npx skills add https://github.com/jackspace/ClaudeSkillz --skill clinpgx-database
Or copy as Structured Prompt for Agent▼
Please help me install this Agent Skill.
Skill: clinpgx-database
Source: https://github.com/jackspace/ClaudeSkillz/tree/main/skills/scientific-db-clinpgx-database
Command: npx skills add https://github.com/jackspace/ClaudeSkillz --skill clinpgx-database

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill requires requests, and includes references (resource) components.

What problem does it solve?

This Skill provides access to ClinPGx pharmacogenomics data (gene-drug interactions, CPIC guidelines, allele functions) for precision medicine workflows and genotype-guided dosing decisions.

Core Features & Use Cases

  • Gene-drug queries, CPIC guidelines, and clinical annotations
  • Allele/phenotype information and frequencies
  • Drug labels and pharmacogenomic annotations
  • Pathways and variant annotations

Quick Start

Install requests, call ClinPGx REST endpoints, and parse JSON responses for integration into clinical decision workflows.

Frequently Asked Questions about clinpgx-database

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I query gene-drug interactions for precision medicine dosing?▼

Gene-drug interactions retrieve CPIC guidelines and allele information through ClinPGx REST API endpoints. Query by gene or drug name to access clinical annotations, phenotype data, and dosing recommendations for genotype-guided clinical decisions.

What pharmacogenomics data does ClinPGx provide for clinical decision support?▼

ClinPGx supplies gene details, drug annotations, allele functions, variant information, and clinical annotations. The database covers CPIC guidelines and drug labels to enable precision dosing workflows in clinical and research settings.

Can I integrate ClinPGx data into my clinical workflow without building custom infrastructure?▼

Yes. ClinPGx REST API endpoints return JSON responses with lightweight authentication and rate limits. Install the requests library and call endpoints directly to parse gene-drug pairs, guidelines, and alleles for immediate integration.

What allele and phenotype information is available for pharmacogenomic research?▼

ClinPGx allele endpoints provide allele functions, phenotype mappings, and variant annotations. Access frequency data and clinical annotations to support pharmacogenomics research and educational analysis of drug metabolism and efficacy.

Does ClinPGx cover drug labels and variant annotations for all genes?▼

ClinPGx covers gene-drug pairs with CPIC clinical annotations and drug label data. Variant and allele endpoints provide annotations; coverage aligns with CPIC guideline scope for clinically actionable pharmacogenomic associations.

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