Generates pharmacogenomic reports from 23andMe/AncestryDNA files: parses 31 SNPs in 12 genes, calls metabolizer phenotypes, maps to CPIC guidance for 51 drugs.
From clawbionpx claudepluginhub clawbio/clawbio --plugin clawbioThis skill uses the workspace's default tool permissions.
api.pydemo_patient.txtdemo_report/report.mdexamples/demo_report.htmlpharmgx_reporter.pytests/test_pharmgx.pyProvides UI/UX resources: 50+ styles, color palettes, font pairings, guidelines, charts for web/mobile across React, Next.js, Vue, Svelte, Tailwind, React Native, Flutter. Aids planning, building, reviewing interfaces.
Fetches up-to-date documentation from Context7 for libraries and frameworks like React, Next.js, Prisma. Use for setup questions, API references, and code examples.
Builds 3-5 year financial models for startups with cohort revenue projections, cost structures, cash flow, headcount plans, burn rate, runway, and scenario analysis.
You are PharmGx Reporter, a specialised ClawBio agent for pharmacogenomic analysis. Your role is to generate a personalised drug–gene interaction report from consumer genetic data.
--drug flag for quick lookup of one medication (used by Drug Photo skill)| Format | Extension | Required Fields | Example |
|---|---|---|---|
| 23andMe raw data | .txt, .txt.gz | rsid, chromosome, position, genotype | demo_patient.txt |
| AncestryDNA raw data | .txt | rsid, chromosome, position, allele1, allele2 | — |
report.md with gene profile table, drug summary, and clinical alerts# Full report from patient data
python skills/pharmgx-reporter/pharmgx_reporter.py \
--input <patient_file> --output <report_dir>
# Demo mode (synthetic 31-SNP patient)
python skills/pharmgx-reporter/pharmgx_reporter.py \
--input skills/pharmgx-reporter/demo_patient.txt --output /tmp/pharmgx_demo
# Single-drug lookup (used by Drug Photo skill)
python skills/pharmgx-reporter/pharmgx_reporter.py \
--input <patient_file> --drug Plavix
# Via ClawBio runner
python clawbio.py run pharmgx --demo
python clawbio.py run pharmgx --input <file> --output <dir>
python clawbio.py run pharmgx --demo
Expected output: A multi-section report covering 12 gene profiles with metaboliser phenotypes, a 51-drug recommendation table (bucketed into AVOID / CAUTION / STANDARD / INSUFFICIENT), and a warfarin special alert (multi-gene CYP2C9 + VKORC1 interaction).
CYP2C19, CYP2D6, CYP2C9, VKORC1, SLCO1B1, DPYD, TPMT, UGT1A1, CYP3A5, CYP2B6, NUDT15, CYP1A2
Antiplatelet, opioids, statins, anticoagulants, PPIs, antidepressants (TCAs, SSRIs, SNRIs), antipsychotics, NSAIDs, oncology, immunosuppressants, antivirals
output_directory/
├── report.md # Full pharmacogenomic report
├── result.json # Machine-readable gene profiles + drug recommendations
└── reproducibility/
└── commands.sh # Exact command to reproduce
Required:
Trigger conditions — the orchestrator routes here when:
Chaining partners:
drug-photo: Single-drug mode powers the photo → dosage card pipelineprofile-report: PharmGx results feed into the unified genomic profileclinpgx: ClinPGx provides deeper gene-drug lookup when the user wants more detail