Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.
8.7
Rating
0
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Data & Analytics
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Excellent pharmacogenomics skill with comprehensive coverage of ClinPGx database capabilities. The description clearly articulates when and how to use the skill for precision medicine applications. Task knowledge is outstanding, providing detailed API examples, complete workflows for clinical decision support, and practical implementation patterns with rate limiting and error handling. Structure is very good, with logical organization from basic queries to complex workflows, though the single-file format is somewhat lengthy (could benefit from separating workflows into a dedicated file). Novelty is strong: querying pharmacogenomics databases requires specialized domain knowledge of gene-drug interactions, CPIC guidelines, allele nomenclature, and clinical evidence levels that would be token-intensive for a general CLI agent to navigate without this skill. The skill meaningfully reduces complexity by providing curated query patterns, phenotype interpretation logic, and clinical workflow templates. Minor improvement could include more modular file organization, but referenced scripts suggest supporting materials exist.
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