rewirebio.iobenchmarks
Configuration

MVP rank score, dbNSFP 5.3.1a (Lee 2026)

MVP rank score, dbNSFP 5.3.1a: dbNSFP 5.3.1a rank score (GRCh38).

3 evaluations · 6 results5 open disagreements between studies involve its model

Overview

An explanatory profile has not yet been reviewed for this record.

Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.

Evaluations and results

3 evaluations · 6 results. Different protocols are not a single leaderboard.

Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels

Sorted by AUROC (CGC missense, all genes) (higher is better). The best value in each column is highlighted. Decimals are rounded for display; each value links to the printed value and its source.

Tested configurationProtocol and datasetAUROC (CGC missense, all genes)AUROC (CGC missense, oncogenes (gain of function))AUROC (CGC missense, tumour suppressors (loss of function))Average precision (CGC missense, all genes)Average precision (CGC missense, oncogenes (gain of function))Average precision (CGC missense, tumour suppressors (loss of function))
MVP rank score, dbNSFP 5.3.1a (Lee 2026)EvaluationCGC missense oncogenicity, all genes (Lee 2026, OncoCal tool_performance.tsv)0.807Not reportedNot reported0.57Not reportedNot reported
MVP rank score, dbNSFP 5.3.1a (Lee 2026)EvaluationCGC missense oncogenicity, oncogenes (gain of function) (Lee 2026, OncoCal tool_performance.tsv)Not reported0.815Not reportedNot reported0.657Not reported
MVP rank score, dbNSFP 5.3.1a (Lee 2026)EvaluationCGC missense oncogenicity, tumour suppressors (loss of function) (Lee 2026, OncoCal tool_performance.tsv)Not reportedNot reported0.803Not reportedNot reported0.502
All 6 result rows with coverage, uncertainty and sources
Filter evaluations

Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: MVP rank score, dbNSFP 5.3.1a (Lee 2026)Protocol: CGC missense oncogenicity, all genes (Lee 2026, OncoCal tool_performance.tsv)
Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels
0.57 Average precision (CGC missense, all genes)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

MVP on CGC missense, all genes (Lee 2026)

somatic-oncogenicity-20261009-protocol-lee2026-all

Aggregation: Not reported

An openly licensed benchmark and per-gene calibration map for missense pathogenicity predictors on activating cancer drivers; OncoCal repository, tables/tool_performance.tsv (per-tool AUROC and AUPRC by gene role) · OncoCal tables/tool_performance.tsv at commit 40b7770f2a76, row tool 'MVP', group 'all', column 'AUPRC'
Configuration: MVP rank score, dbNSFP 5.3.1a (Lee 2026)Protocol: CGC missense oncogenicity, all genes (Lee 2026, OncoCal tool_performance.tsv)
Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels
0.807 AUROC (CGC missense, all genes)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

MVP on CGC missense, all genes (Lee 2026)

somatic-oncogenicity-20261009-protocol-lee2026-all

Aggregation: Not reported

An openly licensed benchmark and per-gene calibration map for missense pathogenicity predictors on activating cancer drivers; OncoCal repository, tables/tool_performance.tsv (per-tool AUROC and AUPRC by gene role) · OncoCal tables/tool_performance.tsv at commit 40b7770f2a76, row tool 'MVP', group 'all', column 'AUROC'
Configuration: MVP rank score, dbNSFP 5.3.1a (Lee 2026)Protocol: CGC missense oncogenicity, oncogenes (gain of function) (Lee 2026, OncoCal tool_performance.tsv)
Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels
0.657 Average precision (CGC missense, oncogenes (gain of function))
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

MVP on CGC missense, oncogenes (gain of function) (Lee 2026)

somatic-oncogenicity-20261009-protocol-lee2026-oncogene

Aggregation: Not reported

An openly licensed benchmark and per-gene calibration map for missense pathogenicity predictors on activating cancer drivers; OncoCal repository, tables/tool_performance.tsv (per-tool AUROC and AUPRC by gene role) · OncoCal tables/tool_performance.tsv at commit 40b7770f2a76, row tool 'MVP', group 'oncogene', column 'AUPRC'
Configuration: MVP rank score, dbNSFP 5.3.1a (Lee 2026)Protocol: CGC missense oncogenicity, oncogenes (gain of function) (Lee 2026, OncoCal tool_performance.tsv)
Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels
0.815 AUROC (CGC missense, oncogenes (gain of function))
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

MVP on CGC missense, oncogenes (gain of function) (Lee 2026)

somatic-oncogenicity-20261009-protocol-lee2026-oncogene

Aggregation: Not reported

An openly licensed benchmark and per-gene calibration map for missense pathogenicity predictors on activating cancer drivers; OncoCal repository, tables/tool_performance.tsv (per-tool AUROC and AUPRC by gene role) · OncoCal tables/tool_performance.tsv at commit 40b7770f2a76, row tool 'MVP', group 'oncogene', column 'AUROC'
Configuration: MVP rank score, dbNSFP 5.3.1a (Lee 2026)Protocol: CGC missense oncogenicity, tumour suppressors (loss of function) (Lee 2026, OncoCal tool_performance.tsv)
Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels
0.502 Average precision (CGC missense, tumour suppressors (loss of function))
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

MVP on CGC missense, tumour suppressors (loss of function) (Lee 2026)

somatic-oncogenicity-20261009-protocol-lee2026-tsg

Aggregation: Not reported

An openly licensed benchmark and per-gene calibration map for missense pathogenicity predictors on activating cancer drivers; OncoCal repository, tables/tool_performance.tsv (per-tool AUROC and AUPRC by gene role) · OncoCal tables/tool_performance.tsv at commit 40b7770f2a76, row tool 'MVP', group 'TSG', column 'AUPRC'
Configuration: MVP rank score, dbNSFP 5.3.1a (Lee 2026)Protocol: CGC missense oncogenicity, tumour suppressors (loss of function) (Lee 2026, OncoCal tool_performance.tsv)
Dataset: Missense variants in 768 Cancer Gene Census genes with open oncogenicity labels
0.803 AUROC (CGC missense, tumour suppressors (loss of function))
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

MVP on CGC missense, tumour suppressors (loss of function) (Lee 2026)

somatic-oncogenicity-20261009-protocol-lee2026-tsg

Aggregation: Not reported

An openly licensed benchmark and per-gene calibration map for missense pathogenicity predictors on activating cancer drivers; OncoCal repository, tables/tool_performance.tsv (per-tool AUROC and AUPRC by gene role) · OncoCal tables/tool_performance.tsv at commit 40b7770f2a76, row tool 'MVP', group 'TSG', column 'AUROC'

Source checking is not independent reproduction. Release 2026-11-02-a7f03c9e55a5.

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Evidence

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Evidence table

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Claims, original sources and review scope · Release 2026-11-02-a7f03c9e55a5
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Sources and history

Release 2026-11-02-a7f03c9e55a5 · Record review: source checked

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

Stable ID: somatic-oncogenicity-20261009-config-lee2026-mvp

areas
dna-genomes
contexts
clinical_research
method types
supervised_machine_learning
reported name
MVP
version
dbNSFP 5.3.1a rank score (GRCh38)
foundation model eligible
false
source locator
OncoCal tool_performance.tsv column 'tool'; preprint Methods 'Features'
provenance note
MVP as scored in the cited benchmark.
Related records

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