Consensus somatic CNV set for the HCC1395/HCC1395BL pair.
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Release 2026-10-09-8eac2440869c · Evidence verified: Not verified
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6 evidence rows matching the loaded filters
| Property and statement | Original source and location | Review and provenance |
|---|---|---|
| attributes.scope_note Per-caller precision and recall are shown only in figures. Context-only references | Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome Results; Table 1; Additional file 5 Version: Genome Biology 25:163, published 2024-06-20; PMC11188507 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; Table 1; Additional file 5 Context-only references | Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome Results; Table 1; Additional file 5 Version: Genome Biology 25:163, published 2024-06-20; PMC11188507 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.split 21 WGS and 12 WES replicates across six centres Context-only references | Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome Results; Table 1; Additional file 5 Version: Genome Biology 25:163, published 2024-06-20; PMC11188507 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.version Genome Biology 2024 Additional file 5 (VCF) Context-only references | Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome Results; Table 1; Additional file 5 Version: Genome Biology 25:163, published 2024-06-20; PMC11188507 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 Consensus somatic CNV set for the HCC1395/HCC1395BL pair. Context-only references | Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome Results; Table 1; Additional file 5 Version: Genome Biology 25:163, published 2024-06-20; PMC11188507 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 SEQC2 HCC1395 high-confidence somatic CNV call set Context-only references | Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome Results; Table 1; Additional file 5 Version: Genome Biology 25:163, published 2024-06-20; PMC11188507 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 |
Release 2026-10-09-8eac2440869c · Record review: discovered
Stable ID: cnv-20261009-data-seqc2-hcc1395-cnv-benchmark