pharmgx-reporterPharmacogenomic report from DTC genetic data (23andMe/AncestryDNA)
Install via ClawdBot CLI:
clawdbot install manuelcorpas/pharmgx-reporterGrade Fair — based on market validation, documentation quality, package completeness, maintenance status, and authenticity signals.
Calls external URL not in known-safe list
https://github.com/ClawBio/ClawBioAudited Apr 17, 2026 · audit v1.0
Generated Mar 20, 2026
Healthcare providers use the tool to analyze patients' genetic data from 23andMe or AncestryDNA to generate pharmacogenomic reports. This helps in tailoring medication plans based on metabolizer phenotypes, reducing adverse drug reactions and improving treatment efficacy in clinical settings.
Researchers in pharmaceutical companies utilize the skill to assess genetic variations across populations for drug development. It aids in identifying potential responders or non-responders to medications, streamlining clinical trials and enhancing drug safety profiles.
Genetic testing companies integrate this tool to offer pharmacogenomic reports as an add-on service. Customers upload their raw data to receive personalized drug recommendations, adding value to existing genetic testing products and promoting precision medicine awareness.
Universities and training programs employ the skill in bioinformatics courses to teach students about pharmacogenomics. It provides hands-on experience with real genetic data, CPIC guidelines, and report generation, fostering skills in precision medicine applications.
Telehealth platforms incorporate the tool to enable remote pharmacogenomic analysis for patients. Doctors can upload genetic files during virtual consultations to quickly access drug recommendations, enhancing decision-making and patient engagement in digital health services.
Offer the tool as a cloud-based service with monthly or annual subscriptions for healthcare providers and researchers. This model ensures recurring revenue through access to updated CPIC data, automated reporting, and API integrations for scalable usage.
Charge users a fee each time they generate a pharmacogenomic report, targeting individual consumers or small clinics. This low-barrier model allows flexible usage without long-term commitments, with revenue generated per analysis transaction.
License the skill to large organizations like pharmaceutical firms or genetic testing companies for internal use. This includes custom integrations, support, and bulk processing capabilities, driving revenue through upfront or annual licensing agreements.
💬 Integration Tip
Ensure input files are in supported formats (23andMe, AncestryDNA, TSV) and validate data parsing to avoid errors in star allele calling and report generation.
Scored Apr 19, 2026
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