Evidence Insight
clinpgx-database
87100Total Score
Core Capability
88 / 100
Functional Suitability
11 / 12
Reliability
10 / 12
Performance & Context
8 / 8
Agent Usability
14 / 16
Human Usability
8 / 8
Security
10 / 12
Maintainability
10 / 12
Agent-Specific
17 / 20
Medical Task
15 / 20 Passed
88Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4
86Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4
86Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4
86Packaged executable path(s): scripts/query_clinpgx.py
3/4
86End-to-end case for Scope-focused workflow aligned to: Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4
Veto GatesRequired pass for any deployment consideration
Skill Veto✓ All 4 gates passed
✓
Operational Stability
System remains stable across varied inputs and edge cases
PASS✓
Structural Consistency
Output structure conforms to expected skill contract format
PASS✓
Result Determinism
Equivalent inputs produce semantically equivalent outputs
PASS✓
System Security
No prompt injection, data leakage, or unsafe tool use detected
PASSResearch Veto✅ PASS — Applicable
| 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 | The older review treated the package logic as methodologically aligned with its stated workflow. |
| Code Usability | PASS | Code usability passed because the search or lookup workflow still exposed a usable entrypoint and output expectation. |
Core Capability88 / 100 — 8 Categories
Functional Suitability
Functional suitability was softened by the legacy issue 'Improve stress-case output rigor'. Stress and boundary scenarios show weaker consistency
11 / 12
92%
Reliability
Related legacy finding for clinpgx-database: Improve stress-case output rigor. Stress and boundary scenarios show weaker consistency
10 / 12
83%
Performance & Context
Performance context reached full score in the archived evaluation.
8 / 8
100%
Agent Usability
The legacy audit deducted points for clinpgx-database in agent usability.
14 / 16
88%
Human Usability
No point loss was recorded for human usability in the legacy audit.
8 / 8
100%
Security
The archived evaluation left some headroom for clinpgx-database under security.
10 / 12
83%
Maintainability
The legacy audit deducted points for clinpgx-database in maintainability.
10 / 12
83%
Agent-Specific
Agent specific was softened by the legacy issue 'Stabilize executable path and fallback behavior'. Some inputs only reached PARTIAL due to execution gaps or weak boundary handling
17 / 20
85%
Core Capability Total88 / 100
Medical TaskExecution Average: 86.4 / 100 — Assertions: 15/20 Passed
88
Canonical
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4 ✓
86
Variant A
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4 ✓
86
Edge
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4 ✓
86
Variant B
Packaged executable path(s): scripts/query_clinpgx.py
3/4 ✓
86
Stress
End-to-end case for Scope-focused workflow aligned to: Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
3/4 ✓
88
Canonical✅ Pass
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when... remains a defined path, although the preserved example command was not directly runnable because placeholder values were never resolved.
Basic 33/40|Specialized 55/60|Total 88/100
✅A1The clinpgx-database output structure matches the documented deliverable
❌A2The script execution path completed successfully for the documented case
✅A3The output stays fully within the documented skill boundary
✅A4The response quality is acceptable for the documented path
Pass rate: 3 / 4
86
Variant A✅ Pass
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
The Access ClinPGx pharmacogenomics data (successor to PharmGKB) when... workflow is specified, but the execution example still depends on unresolved placeholders.
Basic 31/40|Specialized 55/60|Total 86/100
✅A1The clinpgx-database output structure matches the documented deliverable
❌A2The script execution path completed successfully for the documented case
✅A3The output stays fully within the documented skill boundary
✅A4The response quality is acceptable for the documented path
Pass rate: 3 / 4
86
Edge✅ Pass
Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
The archived command path for Access ClinPGx pharmacogenomics data (successor to PharmGKB) when... was structurally clear, yet still placeholder-bound.
Basic 30/40|Specialized 56/60|Total 86/100
✅A1The clinpgx-database output structure matches the documented deliverable
❌A2The script execution path completed successfully for the documented case
✅A3The output stays fully within the documented skill boundary
✅A4The response quality is acceptable for the documented path
Pass rate: 3 / 4
86
Variant B✅ Pass
Packaged executable path(s): scripts/query_clinpgx.py
The Packaged executable path(s): scripts/query_clinpgx.py workflow is specified, but the execution example still depends on unresolved placeholders.
Basic 29/40|Specialized 57/60|Total 86/100
✅A1The clinpgx-database output structure matches the documented deliverable
❌A2The script execution path completed successfully for the documented case
✅A3The output stays fully within the documented skill boundary
✅A4The response quality is acceptable for the documented path
Pass rate: 3 / 4
86
Stress✅ Pass
End-to-end case for Scope-focused workflow aligned to: Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query gene-drug interactions, CPIC guidelines, allele functions, and drug-label PGx content for precision medicine and genotype-guided dosing
The archived command path for Access ClinPGx pharmacogenomics data (successor to PharmGKB) when you need to query... was structurally clear, yet still placeholder-bound.
Basic 26/40|Specialized 60/60|Total 86/100
✅A1The clinpgx-database output structure matches the documented deliverable
❌A2The script execution path completed successfully for the documented case
✅A3The output stays fully within the documented skill boundary
✅A4The response quality is acceptable for the documented path
Pass rate: 3 / 4
Medical Task Total86.4 / 100
Key Strengths
- Primary routing is Evidence Insight with execution mode B
- Static quality score is 88/100 and dynamic average is 73.6/100
- Assertions and command execution outcomes are recorded per input for human review
- Execution verification summary: Script verification 1/1; adjustment=5. query_clinpgx.py: OK