gwas-database
Query the NHGRI-EBI GWAS Catalog to retrieve SNP–trait associations, study metadata, and (when available) summary statistics when you need evidence for a variant, trait/disease, gene, or genomic region.
Veto GatesRequired pass for any deployment consideration
| Dimension | Result | Detail |
|---|---|---|
| Scientific Integrity | PASS | The legacy audit did not indicate that retrieval outputs were presented as unsupported findings. |
| Practice Boundaries | PASS | The package stayed in retrieval, extraction, or evidence-organization scope rather than drifting into unsupported interpretation. |
| Methodological Ground | PASS | No methodological-grounding issue was recorded for gwas-database in the archived evaluation. |
| Code Usability | N/A | The audited artifact centers on document or reasoning outputs, so code usability is not the main evaluation target here. |
Core Capability85 / 100 — 8 Categories
Medical TaskExecution Average: 87.6 / 100 — Assertions: 20/20 Passed
This canonical case stayed inside the documented workflow and remained instruction-led.
Query the NHGRI-EBI GWAS Catalog to retrieve SNP–trait... was evaluated as a bounded documentation path, not as a runnable script workflow.
Multiple query entry points: rsID, EFO trait ID, gene symbol,... was evaluated as a bounded documentation path, not as a runnable script workflow.
Structured entities: studies, associations, variants (SNPs), and... was evaluated as a bounded documentation path, not as a runnable script workflow.
End-to-end case for Multiple query entry points: rsID, EFO trait... was evaluated as a bounded documentation path, not as a runnable script workflow.
Key Strengths
- Primary routing is Evidence Insight with execution mode A
- Static quality score is 85/100 and dynamic average is 79.6/100
- Assertions and command execution outcomes are recorded per input for human review
- Execution verification summary: No script verification was applicable