rewirebio.iobenchmarks
Configuration

iGEMME (Livesey and Marsh 2025)

Configuration of iGEMME: scores from the tool's own published code or score files; no release or settings beyond its name are recorded.

6 evaluations · 7 results

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

6 evaluations · 7 results. Different protocols are not a single leaderboard.

Sorted by Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, 36 human DMS sets) (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 datasetPairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, 36 human DMS sets)Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, direct DMS assays only)Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, indirect DMS assays only)Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, SNV-accessible substitutions only)Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS, SNV-accessible substitutions, missing predictions filled with the VEP's most benign score)Pairwise win rate (average pairwise win rate against all other VEPs, per-protein AUROC on shared variants, ClinVar P/LP versus gnomAD v4.1 missense, proteins with at least 10 of each)Pairwise win rate (average pairwise win rate against the five top-ranked VEPs (column top_5_winrate; the five are not listed in the table), |Spearman| with DMS on shared variants, 36 human DMS sets)
iGEMME (Livesey and Marsh 2025)EvaluationLivesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets, Livesey and Marsh 2025 human DMS benchmark set (36 proteins)86%Not reportedNot reportedNot reportedNot reportedNot reported34.9%
iGEMME (Livesey and Marsh 2025)EvaluationLivesey and Marsh 2025 clinical benchmark: pairwise AUROC win rate, ClinVar pathogenic versus gnomAD missense, Livesey and Marsh 2025 clinical set: ClinVar pathogenic versus gnomAD v4.1 missense (819 proteins)Not reportedNot reportedNot reportedNot reportedNot reported70.4%Not reported
iGEMME (Livesey and Marsh 2025)EvaluationLivesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, direct assays only, Livesey and Marsh 2025 human DMS benchmark set (36 proteins)Not reported89.6%Not reportedNot reportedNot reportedNot reportedNot reported
iGEMME (Livesey and Marsh 2025)EvaluationLivesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, indirect assays only, Livesey and Marsh 2025 human DMS benchmark set (36 proteins)Not reportedNot reported83.4%Not reportedNot reportedNot reportedNot reported
iGEMME (Livesey and Marsh 2025)EvaluationLivesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions with gaps filled, Livesey and Marsh 2025 human DMS benchmark set (36 proteins)Not reportedNot reportedNot reportedNot reported85.8%Not reportedNot reported
iGEMME (Livesey and Marsh 2025)EvaluationLivesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions only, Livesey and Marsh 2025 human DMS benchmark set (36 proteins)Not reportedNot reportedNot reported85.9%Not reportedNot reportedNot reported
All 7 result rows with coverage, uncertainty and sources
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Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 clinical benchmark: pairwise AUROC win rate, ClinVar pathogenic versus gnomAD missense
Dataset: Livesey and Marsh 2025 clinical set: ClinVar pathogenic versus gnomAD v4.1 missense (819 proteins)
70.4% Pairwise win rate (average pairwise win rate against all other VEPs, per-protein AUROC on shared variants, ClinVar P/LP versus gnomAD v4.1 missense, proteins with at least 10 of each)
percent · higher

Uncertainty: Not reported by the source: Figure 3 error bars (standard error across comparisons) are not printed

Coverage: 665/819 proteins with at least 10 ClinVar P/LP and 10 gnomAD missense variants scored by this VEP scored ('proteins' column, cell CJ14)

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 clinical benchmark: pairwise AUROC win rate, ClinVar pathogenic versus gnomAD missense

Livesey and Marsh 2025 clinical benchmark: pairwise AUROC win rate, ClinVar pathogenic versus gnomAD missense

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S8', cell CI14 (row 'iGEMME', column 'rank_score')
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets
Dataset: Livesey and Marsh 2025 human DMS benchmark set (36 proteins)
86% Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, 36 human DMS sets)
percent · higher

Uncertainty: Not reported by the source: Bootstrap standard deviations appear only as Figure 2 error bars; not printed

Coverage: 36/36 human DMS datasets (one per protein) with predictions for this VEP scored ('proteins' column, cell CV6)

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets

Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S3', cell CU6 (row 'iGEMME', column 'rank_score')
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets
Dataset: Livesey and Marsh 2025 human DMS benchmark set (36 proteins)
34.9% Pairwise win rate (average pairwise win rate against the five top-ranked VEPs (column top_5_winrate; the five are not listed in the table), |Spearman| with DMS on shared variants, 36 human DMS sets)
percent · higher

Uncertainty: Not reported by the source: Bootstrap standard deviations appear only as Figure 2 error bars; not printed

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets

Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, all 36 DMS sets

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S3', cell CW6 (row 'iGEMME', column 'top_5_winrate')
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, direct assays only
Dataset: Livesey and Marsh 2025 human DMS benchmark set (36 proteins)
89.6% Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, direct DMS assays only)
percent · higher

Uncertainty: Not reported by the source: Bootstrap standard deviations appear only as Figure 2 error bars; not printed

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, direct assays only

Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, direct assays only

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S5', cell C9 (row 'iGEMME', column 'rank_score_direct')
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, indirect assays only
Dataset: Livesey and Marsh 2025 human DMS benchmark set (36 proteins)
83.4% Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, indirect DMS assays only)
percent · higher

Uncertainty: Not reported by the source: Bootstrap standard deviations appear only as Figure 2 error bars; not printed

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, indirect assays only

Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, indirect assays only

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S5', cell B9 (row 'iGEMME', column 'rank_score_indirect')
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions with gaps filled
Dataset: Livesey and Marsh 2025 human DMS benchmark set (36 proteins)
85.8% Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS, SNV-accessible substitutions, missing predictions filled with the VEP's most benign score)
percent · higher

Uncertainty: Not reported by the source: Bootstrap standard deviations appear only as Figure 2 error bars; not printed

Coverage: 36/36 human DMS datasets (one per protein) with predictions for this VEP scored ('proteins' column, cell C6)

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions with gaps filled

Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions with gaps filled

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S7', cell B6 (row 'iGEMME', column 'rank_score')
Configuration: iGEMME (Livesey and Marsh 2025)Protocol: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions only
Dataset: Livesey and Marsh 2025 human DMS benchmark set (36 proteins)
85.9% Pairwise win rate (average pairwise win rate against all other VEPs, |Spearman| with DMS on shared variants, SNV-accessible substitutions only)
percent · higher

Uncertainty: Not reported by the source: Bootstrap standard deviations appear only as Figure 2 error bars; not printed

Coverage: 36/36 human DMS datasets (one per protein) with predictions for this VEP scored ('proteins' column, cell C6)

Independent external evaluation · Source checked
Methods, coverage and source

iGEMME: Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions only

Livesey and Marsh 2025 DMS benchmark: pairwise |Spearman| win rate, SNV-accessible substitutions only

Aggregation: Not reported

Livesey and Marsh 2025, Supplementary Material 2 (Tables S1-S8); Livesey and Marsh 2025, Genome Biology 26:104 (Europe PMC full text XML) · Supplementary Material 2, sheet 'Table S6', cell B6 (row 'iGEMME', column 'rank_score')

Source checking is not independent reproduction. Release 2026-10-22-1b7cf027e4f6.

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Release 2026-10-22-1b7cf027e4f6 · Record review: source checked

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Technical metadata and extraction receipts

Stable ID: vep-lit-20261014-config-livesey2025-igemme

areas
dna-genomes; proteins-complexes
contexts
research; clinical_research
method types
specialist
reported name
iGEMME
foundation model eligible
false
configuration type
paper_evaluation
version
Predictions obtained from https://zenodo.org/records/10441521 (Table S2 'Source'); release not stated
training overlap
Livesey and Marsh 2025 type: Population-free
access reuse
Livesey and Marsh obtained predictions from: https://zenodo.org/records/10441521
source locator
Supplementary Material 2, Table S2 row 36 ('iGEMME'); printed label 'iGEMME' in Tables S3 and S5-S8
review
reviewer: claude; reviewer note: Claude review agent; no human review claimed. Independent Claude (Opus 5.5) review agent, separate from the extraction agent that built this batch. Automated review only. Transcription, not reproduction.; reviewed at: 2026-10-14T15:30:00Z; artifact sha256: 1b0d792d1a5d3daa95545a7973cabb131c45e42c952e7e5a447a72deef1d1e70; retrieval url: https://static-content.springer.com/esm/art%3A10.1186%2Fs13059-025-03575-w/MediaObjects/13059_2025_3575_MOESM2_ESM.xlsx; method: ai-assisted-source-review; scope-review; method note: Descriptive fields, identity links and missing-metadata reasons checked against the cited sources.; note: Checked; see the dated review for rulings on identity and method type.
provenance note
iGEMME as scored in the Livesey and Marsh 2025 VEP benchmark.
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