rewirebio.iobenchmarks
Dataset

SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)

Cancer cases of the independent SPOT-MAS validation cohort used for tissue-of-origin classification.

Research readiness

These checks assess whether the evidence supports a reproducible investigation. A source-checked score alone does not meet these requirements.

Release 2026-10-09-8cc1db47c7f9 · Evidence verified: Not verified

Evidence incomplete

Replay metrics

Exact outcomes, predictions, identifiers and evaluator are connected.

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Verified: Not verified

Evidence incomplete

Investigate discrepancies

Replay evidence includes annotations and an assessment of dependence. Unknown independence permits descriptive analysis only.

Missing or unresolved evidence

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  • metric replay: verification is missing
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  • dependence: verification is missing

Verified: Not verified

Evidence incomplete

Run locally

A pinned recipe describes the inputs, environment and resource requirements.

Missing or unresolved evidence

  • No verified artifact manifest is linked to this exact record.
  • artifact hashes: verification is missing
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Verified: Not verified

Evidence incomplete

Validate independently

Separate data and exposure records support an independent test.

Missing or unresolved evidence

  • No verified artifact manifest is linked to this exact record.
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Verified: Not verified

Readiness describes the evidence in this release. Availability on your computer is checked separately when an investigation runs. Existing data exposure can prevent independent validation even when files are available.

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No verified artifact manifest is connected to this record yet. The gaps above identify what is needed before analysis can begin.

Read reviewed discrepancy investigations

Evaluation results

3 evaluations · 66 results. Different protocols are not a single leaderboard.

Filter evaluations

Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.69 accuracy
fraction · higher

Uncertainty: Not reported by the source

Coverage: 239 cancer patients scored (n printed in cell B19)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', D19; Validation block; row 'All cancer'; column 'DNN' under 'All stage' (n in B19)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.81 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 67 cancer patients scored (n printed in cell B14)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', D14; Validation block; row 'Breast'; column 'DNN' under 'All stage' (n in B14)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.6 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 53 cancer patients scored (n printed in cell B15)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', D15; Validation block; row 'CRC'; column 'DNN' under 'All stage' (n in B15)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.6 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 5 cancer patients scored (n printed in cell F15)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', H15; Validation block; row 'CRC'; column 'DNN' under 'Stage I' (n in F15)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.69 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 20 cancer patients scored (n printed in cell J15)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', L15; Validation block; row 'CRC'; column 'DNN' under 'Stage II' (n in J15)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.65 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 20 cancer patients scored (n printed in cell N15)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', P15; Validation block; row 'CRC'; column 'DNN' under 'Stage III' (n in N15)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.44 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 8 cancer patients scored (n printed in cell R15)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', T15; Validation block; row 'CRC'; column 'DNN' under 'Non-metastasis with unknown stage' (n in R15)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.41 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 31 cancer patients scored (n printed in cell B16)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', D16; Validation block; row 'Gastric'; column 'DNN' under 'All stage' (n in B16)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
1 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 2 cancer patients scored (n printed in cell F16)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', H16; Validation block; row 'Gastric'; column 'DNN' under 'Stage I' (n in F16)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 5 cancer patients scored (n printed in cell J16)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', L16; Validation block; row 'Gastric'; column 'DNN' under 'Stage II' (n in J16)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.5 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 10 cancer patients scored (n printed in cell N16)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', P16; Validation block; row 'Gastric'; column 'DNN' under 'Stage III' (n in N16)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.4 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 14 cancer patients scored (n printed in cell R16)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', T16; Validation block; row 'Gastric'; column 'DNN' under 'Non-metastasis with unknown stage' (n in R16)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.77 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 45 cancer patients scored (n printed in cell B17)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', D17; Validation block; row 'Liver'; column 'DNN' under 'All stage' (n in B17)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
1 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 2 cancer patients scored (n printed in cell F17)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', H17; Validation block; row 'Liver'; column 'DNN' under 'Stage I' (n in F17)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
1 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 10 cancer patients scored (n printed in cell J17)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', L17; Validation block; row 'Liver'; column 'DNN' under 'Stage II' (n in J17)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.86 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 15 cancer patients scored (n printed in cell N17)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', P17; Validation block; row 'Liver'; column 'DNN' under 'Stage III' (n in N17)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
1 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 18 cancer patients scored (n printed in cell R17)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', T17; Validation block; row 'Liver'; column 'DNN' under 'Non-metastasis with unknown stage' (n in R17)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.74 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 43 cancer patients scored (n printed in cell B18)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', D18; Validation block; row 'Lung'; column 'DNN' under 'All stage' (n in B18)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
N/A recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 0 cancer patients scored (n printed in cell F18)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', H18; Validation block; row 'Lung'; column 'DNN' under 'Stage I' (n in F18)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 3 cancer patients scored (n printed in cell J18)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', L18; Validation block; row 'Lung'; column 'DNN' under 'Stage II' (n in J18)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.79 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 24 cancer patients scored (n printed in cell N18)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', P18; Validation block; row 'Lung'; column 'DNN' under 'Stage III' (n in N18)
Configuration: SPOT-MAS tissue-of-origin Deep neural network (DNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.58 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 16 cancer patients scored (n printed in cell R18)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, DNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', T18; Validation block; row 'Lung'; column 'DNN' under 'Non-metastasis with unknown stage' (n in R18)
Configuration: SPOT-MAS tissue-of-origin Graph convolutional neural network (GCNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.69 accuracy
fraction · higher

Uncertainty: Not reported by the source

Coverage: 239 cancer patients scored (n printed in cell B19)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, GCNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', E19; Validation block; row 'All cancer'; column 'GCNN' under 'All stage' (n in B19)
Configuration: SPOT-MAS tissue-of-origin Graph convolutional neural network (GCNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.78 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 67 cancer patients scored (n printed in cell B14)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, GCNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', E14; Validation block; row 'Breast'; column 'GCNN' under 'All stage' (n in B14)
Configuration: SPOT-MAS tissue-of-origin Graph convolutional neural network (GCNN)Protocol: SPOT-MAS five-class tissue of origin, independent validation cohort
Dataset: SPOT-MAS validation cohort, 239 non-metastatic cancer patients (five cancer types)
0.66 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: 53 cancer patients scored (n printed in cell B15)

Author-reported evaluation · Source checked
Methods, coverage and source

SPOT-MAS tissue of origin, GCNN (validation)

ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation

Aggregation: Not reported

Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization; Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11) · Supplementary file 1, sheet 'Table S9', E15; Validation block; row 'CRC'; column 'GCNN' under 'All stage' (n in B15)

Source checking is not independent reproduction. Release 2026-10-09-8cc1db47c7f9.

Dataset and evaluation context

A dataset supplies biological observations. The evaluation protocol defines how those observations are split, used and scored.

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.

16 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-10-09-8cc1db47c7f9
Property and statementOriginal source and locationReview and provenance
attributes.assay
SPOT-MAS: one plasma cfDNA bisulfite library; 450-region target capture (~52x) and shallow genome-wide fraction (~0.55x)
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: eLife 12:RP89083, version of record published 2023-10-11; PMC10567114 full-text XML
Retrieved: 2026-10-09T20:04:09Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.assay

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.assay
SPOT-MAS: one plasma cfDNA bisulfite library; 450-region target capture (~52x) and shallow genome-wide fraction (~0.55x)
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: Supplementary file 1 (elife-89083-supp1.xlsx) of eLife 12:RP89083, PMC open-access copy PMC10567114.1
Retrieved: 2026-10-09T20:03:58Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.assay

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.population
239 treatment-naive non-metastatic patients: 67 breast, 53 colorectal, 31 gastric, 45 liver, 43 lung; recruited in Vietnam
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: eLife 12:RP89083, version of record published 2023-10-11; PMC10567114 full-text XML
Retrieved: 2026-10-09T20:04:09Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.population

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.population
239 treatment-naive non-metastatic patients: 67 breast, 53 colorectal, 31 gastric, 45 liver, 43 lung; recruited in Vietnam
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: Supplementary file 1 (elife-89083-supp1.xlsx) of eLife 12:RP89083, PMC open-access copy PMC10567114.1
Retrieved: 2026-10-09T20:03:58Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.population

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.source_locator
Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: eLife 12:RP89083, version of record published 2023-10-11; PMC10567114 full-text XML
Retrieved: 2026-10-09T20:04:09Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.source_locator

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.source_locator
Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: Supplementary file 1 (elife-89083-supp1.xlsx) of eLife 12:RP89083, PMC open-access copy PMC10567114.1
Retrieved: 2026-10-09T20:03:58Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.source_locator

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.split
Random assignment of participants to discovery and validation cohorts; validation used only for evaluation
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: eLife 12:RP89083, version of record published 2023-10-11; PMC10567114 full-text XML
Retrieved: 2026-10-09T20:04:09Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.split

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.split
Random assignment of participants to discovery and validation cohorts; validation used only for evaluation
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: Supplementary file 1 (elife-89083-supp1.xlsx) of eLife 12:RP89083, PMC open-access copy PMC10567114.1
Retrieved: 2026-10-09T20:03:58Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.split

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.total
239
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: eLife 12:RP89083, version of record published 2023-10-11; PMC10567114 full-text XML
Retrieved: 2026-10-09T20:04:09Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.total

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.total
239
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9

Shared locator for this statement’s cited sources; not a separate locator for each citation.

Version: Supplementary file 1 (elife-89083-supp1.xlsx) of eLife 12:RP89083, PMC open-access copy PMC10567114.1
Retrieved: 2026-10-09T20:03:58Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.total

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Sources and history

Release 2026-10-09-8cc1db47c7f9 · Record review: source checked

2 source records and release historyDownload this release (gzip)
Technical metadata and extraction receipts

Stable ID: ctdnameth-20261009-data-nguyen2023-spotmas-validation-cancers

areas
dna-genomes
contexts
clinical_research
version
eLife 12:RP89083 (2023)
population
239 treatment-naive non-metastatic patients: 67 breast, 53 colorectal, 31 gastric, 45 liver, 43 lung; recruited in Vietnam
split
Random assignment of participants to discovery and validation cohorts; validation used only for evaluation
total
239
assay
SPOT-MAS: one plasma cfDNA bisulfite library; 450-region target capture (~52x) and shallow genome-wide fraction (~0.55x)
source locator
Article Results 'Clinical characteristics' (P6, P8); Table 1; Supplementary file 1 Table S9
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