compared_database_releases: rare-reanalysis-20261009-protocol-vestito2024-new-candidate-flagging
Descriptive fact transcribed from the pinned source.
Evidence
Source checking verifies the cited claim or transcription. It does not establish independent reproduction.
Evidence table
Inspect claims, sources and review details
Trace each statement to its source and review. A context-only reference supports the record generally; it does not verify an individual field. Source checking does not reproduce an experiment.
One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.
6 evidence rows matching the loaded filters
| Property and statement | Original source and location | Review and provenance |
|---|---|---|
| attributes.field compared_database_releases Context-only references | Efficient reinterpretation of rare disease cases using Exomiser Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Version: npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML | 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.source_locator Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Context-only references | Efficient reinterpretation of rare disease cases using Exomiser Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Version: npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML | 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.value Results paragraph 6 reports that, comparing Exomiser results based on the February 2019 and February 2022 databases, a variant score above 0.8 with a human phenotype score increase of 0.2 highlights 54 new candidates in the 37 cases, 31 of them correct (recall 84%, precision 57%). Supplementary Table 1 prints TP 31 and FP 23 (31 + 23 = 54) for that setting, so the table is read as that comparison; the table itself does not name the releases. Context-only references | Efficient reinterpretation of rare disease cases using Exomiser Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Version: npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML | 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 Descriptive fact transcribed from the pinned source. Context-only references | Efficient reinterpretation of rare disease cases using Exomiser Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Version: npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML | 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: subject rare-reanalysis-20261009-protocol-vestito2024-new-candidate-flagging Context-only references | Efficient reinterpretation of rare disease cases using Exomiser Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Version: npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML | 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 compared_database_releases: rare-reanalysis-20261009-protocol-vestito2024-new-candidate-flagging Context-only references | Efficient reinterpretation of rare disease cases using Exomiser Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8' Version: npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML | 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
Release 2026-10-10-6e93f504adfc · Record review: source checked
1 source records and release history
- Efficient reinterpretation of rare disease cases using Exomiser · Original source · npj Genomic Medicine 9:65, published 2024-12-18; PMC11655964 full-text XML
Technical metadata and extraction receipts
Stable ID: rare-reanalysis-20261009-claim-vestito2024-database-pair
- field
- compared_database_releases
- value
- Results paragraph 6 reports that, comparing Exomiser results based on the February 2019 and February 2022 databases, a variant score above 0.8 with a human phenotype score increase of 0.2 highlights 54 new candidates in the 37 cases, 31 of them correct (recall 84%, precision 57%). Supplementary Table 1 prints TP 31 and FP 23 (31 + 23 = 54) for that setting, so the table is read as that comparison; the table itself does not name the releases.
- source locator
- Results paragraph 6; Supplementary Table 1 row 'Diff human score 0.2, Var score 0.8'
- review
- method: source-hash-verification; ai-assisted-source-review; method note: Re-downloaded the article XML and matched its SHA-256, extracted the cited paragraphs and tables with a separate parser and compared the claim text with them.; reviewer: claude; reviewer note: Separate Claude review agent, independent of the extractor; no human review claimed; date: 2026-10-09; artifact sha256: b8cd48ed7e4a337ddf954d1b9bb004305ac78c383268592828e6203418d04058; retrieval url: https://www.ebi.ac.uk/europepmc/webservices/rest/PMC11655964/fullTextXML; note: Transcribed from the pinned source. Independent review 2026-10-09: Matches Results paragraph 6 (54 candidates, 31 correct, recall 84%, precision 57%) and the 0.2/0.8 row (TP 31, FP 23; 31/37 = 0.838, 31/54 = 0.574). The claim states the reading as an inference, which it is: the table does not name the releases.