rewirebio.iobenchmarks
Evaluation

SPOT-MAS tissue of origin, GCNN (validation)

Published comparison; transcribed, not reproduced.

Research readiness

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

Evidence incomplete

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Investigate discrepancies

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Verified: Not verified

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Evaluation results

1 evaluation · 22 results. Different protocols are not a single leaderboard.

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Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
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)
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)
0.6 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, 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', I15; Validation block; row 'CRC'; column 'GCNN' under 'Stage I' (n in F15)
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)
0.56 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, 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', M15; Validation block; row 'CRC'; column 'GCNN' under 'Stage II' (n in J15)
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)
0.75 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, 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', Q15; Validation block; row 'CRC'; column 'GCNN' under 'Stage III' (n in N15)
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)
0.67 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, 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', U15; Validation block; row 'CRC'; column 'GCNN' under 'Non-metastasis with unknown stage' (n in R15)
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)
0.55 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, 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', E16; Validation block; row 'Gastric'; column 'GCNN' under 'All stage' (n in B16)
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)
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, 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', I16; Validation block; row 'Gastric'; column 'GCNN' under 'Stage I' (n in F16)
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)
0.8 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, 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', M16; Validation block; row 'Gastric'; column 'GCNN' under 'Stage II' (n in J16)
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)
0.7 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, 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', Q16; Validation block; row 'Gastric'; column 'GCNN' under 'Stage III' (n in N16)
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)
0.29 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, 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', U16; Validation block; row 'Gastric'; column 'GCNN' under 'Non-metastasis with unknown stage' (n in R16)
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)
0.76 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, 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', E17; Validation block; row 'Liver'; column 'GCNN' under 'All stage' (n in B17)
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)
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, 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', I17; Validation block; row 'Liver'; column 'GCNN' under 'Stage I' (n in F17)
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)
0.9 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, 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', M17; Validation block; row 'Liver'; column 'GCNN' under 'Stage II' (n in J17)
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)
0.8 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, 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', Q17; Validation block; row 'Liver'; column 'GCNN' under 'Stage III' (n in N17)
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)
0.61 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, 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', U17; Validation block; row 'Liver'; column 'GCNN' under 'Non-metastasis with unknown stage' (n in R17)
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)
0.63 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, 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', E18; Validation block; row 'Lung'; column 'GCNN' under 'All stage' (n in B18)
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)
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, 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', I18; Validation block; row 'Lung'; column 'GCNN' under 'Stage I' (n in F18)
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)
0.34 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, 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', M18; Validation block; row 'Lung'; column 'GCNN' under 'Stage II' (n in J18)
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)
0.67 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, 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', Q18; Validation block; row 'Lung'; column 'GCNN' under 'Stage III' (n in N18)
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)
0.62 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, 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', U18; Validation block; row 'Lung'; column 'GCNN' under 'Non-metastasis with unknown stage' (n in R18)

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

Evaluation procedure

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

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)
origin
Author-reported evaluation
configuration
Primary source as retrieved 2026-10-09
protocol id
ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation
dataset version
eLife 12:RP89083
split
Independent validation cohort
population
239 cancer patients, five types
inputs
Nine concatenated SPOT-MAS cfDNA feature sets
adaptation
Not reported
metric implementation
Correctly assigned patients / patients in the stratum
aggregation
Per cancer type and stage stratum
budget
Not reported

Metadata review: source checked. Unreported conditions prevent automatic comparisons.

Reproduction

Split
Independent validation cohort
Adaptation
Not reported
Scoring implementation
Correctly assigned patients / patients in the stratum

No execution recipe has been verified for this exact configuration and evaluation. A benchmark's general instructions may use different inputs, splits or model settings.

Reproducing this published result requires matching its model configuration, data, split and scorer. Source checking or a successful smoke test does not establish score reproduction.

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.

36 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.comparison.adaptation
Not reported
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

missing or unspecified

No individual claim review recorded

author reported

Audit details

Field: attributes.comparison.adaptation

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

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

Inspected artifact

attributes.comparison.adaptation
Not reported
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

missing or unspecified

No individual claim review recorded

author reported

Audit details

Field: attributes.comparison.adaptation

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

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

Inspected artifact

attributes.comparison.aggregation
Per cancer type and stage stratum
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

author reported

Audit details

Field: attributes.comparison.aggregation

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

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

Inspected artifact

attributes.comparison.aggregation
Per cancer type and stage stratum
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

author reported

Audit details

Field: attributes.comparison.aggregation

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

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

Inspected artifact

attributes.comparison.budget
Not reported
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

missing or unspecified

No individual claim review recorded

author reported

Audit details

Field: attributes.comparison.budget

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

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

Inspected artifact

attributes.comparison.budget
Not reported
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

missing or unspecified

No individual claim review recorded

author reported

Audit details

Field: attributes.comparison.budget

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

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

Inspected artifact

attributes.comparison.dataset_version
eLife 12:RP89083
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

author reported

Audit details

Field: attributes.comparison.dataset_version

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

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

Inspected artifact

attributes.comparison.dataset_version
eLife 12:RP89083
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

author reported

Audit details

Field: attributes.comparison.dataset_version

Source artifact SHA-256: 4797d7ea0fde127bfa54cf0bdf717d859092c0442ab996a0af10cc5ce17b7331

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

Inspected artifact

attributes.comparison.inputs
Nine concatenated SPOT-MAS cfDNA feature sets
Context-only references
Multimodal analysis of methylomics and fragmentomics in plasma cell-free DNA for multi-cancer early detection and localization

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

author reported

Audit details

Field: attributes.comparison.inputs

Source artifact SHA-256: e09cfb58a6055e89ffa7b553a37539e1687f0fcb26970b7b25eb9eda8e09cfa8

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

Inspected artifact

attributes.comparison.inputs
Nine concatenated SPOT-MAS cfDNA feature sets
Context-only references
Nguyen et al. 2023, Supplementary file 1 (Tables S1-S11)

Original source ↗

Supplementary file 1 Table S9, GCNN columns, rows 14-19

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

author reported

Audit details

Field: attributes.comparison.inputs

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-eval-nguyen2023-spotmas-too-gcnn-validation

areas
dna-genomes
contexts
clinical_research
origin
author_reported
protocol
ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation
version
Primary source as retrieved 2026-10-09
comparison
protocol id: ctdnameth-20261009-protocol-nguyen2023-spotmas-too-validation; dataset version: eLife 12:RP89083; split: Independent validation cohort; population: 239 cancer patients, five types; inputs: Nine concatenated SPOT-MAS cfDNA feature sets; adaptation: Not reported; metric implementation: Correctly assigned patients / patients in the stratum; aggregation: Per cancer type and stage stratum; budget: Not reported
source locator
Supplementary file 1 Table S9, GCNN columns, rows 14-19
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