Generic BayesDel computational-evidence threshold baseline
Source-supported generic threshold alternative to gene-specific ENIGMA categories; scope is functional-reference evidence code assignment.
Evaluation results
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Source checking is not independent reproduction. Release 2026-09-30-e37e3ab1284d.
Applicable tests and references
Applicability is distinct from a completed evaluation.
- BRCA1 generic BayesDel threshold evidence-code assignment · Proposed association
- BRCA2 generic BayesDel threshold evidence-code assignment · Proposed association
Evidence
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Evidence table
Inspect claims, sources and review details
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One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.
7 evidence rows matching the loaded filters
| Property and statement | Original source and location | Review and provenance |
|---|---|---|
| attributes.applicability source_supported Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.baseline_type conventional_workflow Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| description Source-supported generic threshold alternative to gene-specific ENIGMA categories; scope is functional-reference evidence code assignment. Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| Relationship: applicable to uc-clinical-20260930-enigma-brca1-generic-protocol Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| Relationship: applicable to uc-clinical-20260930-enigma-brca2-generic-protocol Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| Relationship: configuration uc-clinical-20260930-bayesdel-pejaver-generic Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| name Generic BayesDel computational-evidence threshold baseline Context-only references | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel No field-specific location recorded Version: 2024 final article; reported VCEP specifications v1.0 | not individually reviewed No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
Sources and history
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Release 2026-09-30-e37e3ab1284d · Record review: source checked
1 source records and release history
- Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel · Original source · 2024 final article; reported VCEP specifications v1.0
Technical metadata and extraction receipts
Stable ID: uc-clinical-20260930-baseline-bayesdel-generic
- areas
- dna-genomes
- contexts
- clinical_research
- baseline type
- conventional_workflow
- applicability
- source_supported
- review
- method: automated_source_review; reviewer: Codex clinical coverage worker; date: 2026-09-30; note: Transcription from inspected primary source. No execution, independent replication or human scientific review.; source id: uc-clinical-20260930-source-enigma
Related records
- configuration: BayesDel generic Pejaver evidence thresholds in ENIGMA comparison
- applicable to: BRCA1 generic BayesDel threshold evidence-code assignment
- applicable to: BRCA2 generic BayesDel threshold evidence-code assignment