rewirebio.iobenchmarks
Configuration

Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)

Evo 2 7B base model scoring a variant as the log-likelihood of the alternative minus the reference 8,192 bp sequence.

14 evaluations · 14 results1 open disagreement between studies involves 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

14 evaluations · 14 results. Different protocols are not a single leaderboard.

Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)

Sorted by AUROC (ClinVar pathogenic vs benign SNVs, 3' UTR) (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 (ClinVar pathogenic vs benign SNVs, 3' UTR)AUROC (ClinVar pathogenic vs benign SNVs, 5' UTR)AUROC (ClinVar pathogenic vs benign SNVs, All variants)AUROC (ClinVar pathogenic vs benign SNVs, Intron (Non-splice))AUROC (ClinVar pathogenic vs benign SNVs, Missense & 3'UTR)AUROC (ClinVar pathogenic vs benign SNVs, Missense & Intron (Non-splice))AUROC (ClinVar pathogenic vs benign SNVs, Missense)AUROC (ClinVar pathogenic vs benign SNVs, Noncoding)AUROC (ClinVar pathogenic vs benign SNVs, RNA gene)AUROC (ClinVar pathogenic vs benign SNVs, Splice)AUROC (ClinVar pathogenic vs benign SNVs, Start loss)AUROC (ClinVar pathogenic vs benign SNVs, Stop gain)AUROC (ClinVar pathogenic vs benign SNVs, Stop loss)AUROC (ClinVar pathogenic vs benign SNVs, Synonymous)
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: 3' UTR (Figure 1)0.747Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: All variants (Figure 1)Not reportedNot reported0.969Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Intron (Non-splice) (Figure 1)Not reportedNot reportedNot reported0.903Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Missense & Intron (Non-splice) (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reported0.835Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Missense & 3'UTR (Figure 1)Not reportedNot reportedNot reportedNot reported0.896Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Missense (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reported0.836Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Noncoding (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.975Not reportedNot reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: RNA gene (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.459Not reportedNot reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Splice (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.697Not reportedNot reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Start loss (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.711Not reportedNot reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Stop gain (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.663Not reportedNot reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Stop loss (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.826Not reported
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Synonymous (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.885
Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: 5' UTR (Figure 1)Not reported0.767Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
All 14 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: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: All variants (Figure 1)
0.969 AUROC (ClinVar pathogenic vs benign SNVs, All variants)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar All variants SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 1, panel 1 'All variants (N=258,944, %P=30.59%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Intron (Non-splice) (Figure 1)
0.903 AUROC (ClinVar pathogenic vs benign SNVs, Intron (Non-splice))
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Intron (Non-splice) SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 1, panel 3 'Intron (Non-splice) (N=88,049, %P=1.60%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Missense & Intron (Non-splice) (Figure 1)
0.835 AUROC (ClinVar pathogenic vs benign SNVs, Missense & Intron (Non-splice))
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Missense & Intron (Non-splice) SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 3, panel 2 'Missense & Intron (Non-splice) (N=255, %P=17.91%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Missense & 3'UTR (Figure 1)
0.896 AUROC (ClinVar pathogenic vs benign SNVs, Missense & 3'UTR)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Missense & 3'UTR SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 3, panel 3 'Missense & 3'UTR (N=117, %P=40.97%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Missense (Figure 1)
0.836 AUROC (ClinVar pathogenic vs benign SNVs, Missense)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Missense SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 3, panel 1 'Missense (N=50,820, %P=40.09%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Noncoding (Figure 1)
0.975 AUROC (ClinVar pathogenic vs benign SNVs, Noncoding)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Noncoding SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 1, panel 2 'Noncoding (N=118,256, %P=10.69%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: RNA gene (Figure 1)
0.459 AUROC (ClinVar pathogenic vs benign SNVs, RNA gene)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar RNA gene SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 2, panel 2 'RNA gene (N=131, %P=25.95%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Splice (Figure 1)
0.697 AUROC (ClinVar pathogenic vs benign SNVs, Splice)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Splice SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 1, panel 4 'Splice (N=11,042, %P=99.30%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Start loss (Figure 1)
0.711 AUROC (ClinVar pathogenic vs benign SNVs, Start loss)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Start loss SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 2, panel 5 'Start loss (N=847, %P=97.53%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Stop gain (Figure 1)
0.663 AUROC (ClinVar pathogenic vs benign SNVs, Stop gain)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Stop gain SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 3, panel 4 'Stop gain (N=42,408, %P=98.13%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Stop loss (Figure 1)
0.826 AUROC (ClinVar pathogenic vs benign SNVs, Stop loss)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Stop loss SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 2, panel 4 'Stop loss (N=94, %P=75.53%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: Synonymous (Figure 1)
0.885 AUROC (ClinVar pathogenic vs benign SNVs, Synonymous)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar Synonymous SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 2, panel 3 'Synonymous (N=42,139, %P=0.66%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: 3' UTR (Figure 1)
0.747 AUROC (ClinVar pathogenic vs benign SNVs, 3' UTR)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar 3' UTR SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 1, panel 5 '3' UTR (N=11,851, %P=0.21%)', row 'Evo2', bar label
Configuration: Evo 2 7B base, 8,192 bp log-likelihood ratio (Lu et al. 2025)Protocol: ClinVar pathogenic versus benign SNVs within variant type, AUROC (Lu et al. 2025)
Dataset subset: Lu et al. 2025 ClinVar benchmark: 5' UTR (Figure 1)
0.767 AUROC (ClinVar pathogenic vs benign SNVs, 5' UTR)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Evo2 on ClinVar 5' UTR SNVs (Lu et al. 2025 Figure 1)

lu-hetero-20261019-protocol-clinvar-variant-type-auroc

Aggregation: Not reported

Genomic heterogeneity inflates the performance of variant pathogenicity predictions (Lu, Liu, Lin and Brandes, bioRxiv 2025, v2) · Figure 1 (page 8), column 2, panel 1 '5' UTR (N=2,471, %P=2.38%)', row 'Evo2', bar label

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

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

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Technical metadata and extraction receipts

Stable ID: lu-hetero-20261019-config-evo2-7b-base-llr

areas
dna-genomes
contexts
clinical_research
method types
foundation_model
reported name
Evo2
parameters
evo2_7b_base from the Evo2 GitHub repository; 8,192 bp centred window; model.score_sequences on reference and alternative; score multiplied by -1.
source locator
Methods 'Evo2' (pages 13 to 14)
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