rewirebio.iobenchmarks
Configuration

RNA-FM (Evo 2 paper variant effect evaluations)

Configuration of RNA-FM: RNA language model; checkpoint not stated.

26 evaluations · 52 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

26 evaluations · 52 results. Different protocols are not a single leaderboard.

Sorted by AUPRC (zero-shot; BRCA1 'Both' (coding and noncoding) SNVs) (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 datasetAUPRC (zero-shot; BRCA1 'Both' (coding and noncoding) SNVs)AUPRC (zero-shot; BRCA1 coding SNVs)AUPRC (zero-shot; BRCA1 intronic SNVs)AUPRC (zero-shot; BRCA1 noncoding SNVs)AUPRC (zero-shot; BRCA1 splice region SNVs)AUPRC (zero-shot; BRCA2 noncoding SNVs)AUPRC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs)AUPRC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs)AUPRC (zero-shot; ClinVar noncoding indels)AUPRC (zero-shot; ClinVar noncoding microsatellite variants)AUPRC (zero-shot; ClinVar noncoding non-SNVs, far from splice site)AUPRC (zero-shot; ClinVar noncoding non-SNVs, highly conserved)AUPRC (zero-shot; ClinVar noncoding non-SNVs, intergenic)AUPRC (zero-shot; ClinVar noncoding non-SNVs, moderately conserved)AUPRC (zero-shot; ClinVar noncoding non-SNVs, near splice site)AUPRC (zero-shot; ClinVar noncoding non-SNVs, not conserved)AUPRC (zero-shot; ClinVar noncoding non-SNVs, poorly conserved)AUPRC (zero-shot; ClinVar noncoding SNVs, far from splice site)AUPRC (zero-shot; ClinVar noncoding SNVs, highly conserved)AUPRC (zero-shot; ClinVar noncoding SNVs, intergenic)AUPRC (zero-shot; ClinVar noncoding SNVs, moderately conserved)AUPRC (zero-shot; ClinVar noncoding SNVs, near splice site)AUPRC (zero-shot; ClinVar noncoding SNVs, not conserved)AUPRC (zero-shot; ClinVar noncoding SNVs, poorly conserved)AUPRC (zero-shot; SpliceVarDB 'Both' (coding and noncoding) SNVs)AUPRC (zero-shot; SpliceVarDB exonic SNVs)AUROC (zero-shot; BRCA1 'Both' (coding and noncoding) SNVs)AUROC (zero-shot; BRCA1 coding SNVs)AUROC (zero-shot; BRCA1 intronic SNVs)AUROC (zero-shot; BRCA1 noncoding SNVs)AUROC (zero-shot; BRCA1 splice region SNVs)AUROC (zero-shot; BRCA2 noncoding SNVs)AUROC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs)AUROC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs)AUROC (zero-shot; ClinVar noncoding indels)AUROC (zero-shot; ClinVar noncoding microsatellite variants)AUROC (zero-shot; ClinVar noncoding non-SNVs, far from splice site)AUROC (zero-shot; ClinVar noncoding non-SNVs, highly conserved)AUROC (zero-shot; ClinVar noncoding non-SNVs, intergenic)AUROC (zero-shot; ClinVar noncoding non-SNVs, moderately conserved)AUROC (zero-shot; ClinVar noncoding non-SNVs, near splice site)AUROC (zero-shot; ClinVar noncoding non-SNVs, not conserved)AUROC (zero-shot; ClinVar noncoding non-SNVs, poorly conserved)AUROC (zero-shot; ClinVar noncoding SNVs, far from splice site)AUROC (zero-shot; ClinVar noncoding SNVs, highly conserved)AUROC (zero-shot; ClinVar noncoding SNVs, intergenic)AUROC (zero-shot; ClinVar noncoding SNVs, moderately conserved)AUROC (zero-shot; ClinVar noncoding SNVs, near splice site)AUROC (zero-shot; ClinVar noncoding SNVs, not conserved)AUROC (zero-shot; ClinVar noncoding SNVs, poorly conserved)AUROC (zero-shot; SpliceVarDB 'Both' (coding and noncoding) SNVs)AUROC (zero-shot; SpliceVarDB exonic SNVs)
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot BRCA1 'Both' (coding and noncoding) SNVs classification (Evo 2 paper, Supplementary Data 1), BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)0.206Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.493Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot BRCA1 coding SNVs classification (Evo 2 paper, Supplementary Data 1), BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)Not reported0.21Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.497Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot BRCA1 intronic SNVs classification (Evo 2 paper, Supplementary Data 1), BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)Not reportedNot reported0.016Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.389Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot BRCA1 noncoding SNVs classification (Evo 2 paper, Supplementary Data 1), BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)Not reportedNot reportedNot reported0.208Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.468Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot BRCA1 splice region SNVs classification (Evo 2 paper, Supplementary Data 1), BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reported0.428Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.487Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot BRCA2 noncoding SNVs classification (Evo 2 paper, Supplementary Data 1), BRCA2 SNVs with functional classifications, Huang et al. 2025 (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reported0.312Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.54Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reported0.015Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.508Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.004Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.536Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding indels classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.187Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.513Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding microsatellite variants classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.013Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.617Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.07Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.51Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.746Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.517Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, intergenic classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.71Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.625Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.182Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.528Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, near splice site classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.519Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.514Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.07Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.502Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding non-SNVs, poorly conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.036Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.569Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.016Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.551Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.901Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.52Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, intergenic classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.274Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.519Not reportedNot reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, moderately conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.075Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.52Not reportedNot reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, near splice site classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.824Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.503Not reportedNot reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, not conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.014Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.601Not reportedNot reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot ClinVar noncoding SNVs, poorly conserved classification (Evo 2 paper, Supplementary Data 1), ClinVar October 2024 release, filtered (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.031Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.574Not reportedNot reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot SpliceVarDB 'Both' (coding and noncoding) SNVs classification (Evo 2 paper, Supplementary Data 1), SpliceVarDB experimentally validated splice variants (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.627Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.531Not reported
RNA-FM (Evo 2 paper variant effect evaluations)EvaluationZero-shot SpliceVarDB exonic SNVs classification (Evo 2 paper, Supplementary Data 1), SpliceVarDB experimentally validated splice variants (Brixi et al. 2026)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.421Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.56
All 52 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: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 'Both' (coding and noncoding) SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.206 AUPRC (zero-shot; BRCA1 'Both' (coding and noncoding) SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 'Both' (coding and noncoding) SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-both-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J647, row 647: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Both', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 'Both' (coding and noncoding) SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.493 AUROC (zero-shot; BRCA1 'Both' (coding and noncoding) SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 'Both' (coding and noncoding) SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-both-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I647, row 647: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Both', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 coding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.21 AUPRC (zero-shot; BRCA1 coding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 coding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-coding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J648, row 648: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 coding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.497 AUROC (zero-shot; BRCA1 coding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 coding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-coding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I648, row 648: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Coding', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 intronic SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.016 AUPRC (zero-shot; BRCA1 intronic SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 intronic SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-intronic-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J699, row 699: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Intronic', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 intronic SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.389 AUROC (zero-shot; BRCA1 intronic SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 intronic SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-intronic-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I699, row 699: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Intronic', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 noncoding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.208 AUPRC (zero-shot; BRCA1 noncoding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 noncoding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-noncoding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J649, row 649: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Noncoding', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 noncoding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.468 AUROC (zero-shot; BRCA1 noncoding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 noncoding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-noncoding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I649, row 649: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Noncoding', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 splice region SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.428 AUPRC (zero-shot; BRCA1 splice region SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 splice region SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-splice-region-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J684, row 684: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Splice region', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA1 splice region SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA1 saturation genome editing SNVs, Findlay et al. 2018 classes (Brixi et al. 2026)
0.487 AUROC (zero-shot; BRCA1 splice region SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA1 splice region SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca1-splice-region-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I684, row 684: Model 'RNA-FM', Data 'BRCA1', Genomic_Feature 'Splice region', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA2 noncoding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA2 SNVs with functional classifications, Huang et al. 2025 (Brixi et al. 2026)
0.312 AUPRC (zero-shot; BRCA2 noncoding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA2 noncoding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca2-noncoding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J560, row 560: Model 'RNA-FM', Data 'BRCA2', Genomic_Feature 'Noncoding', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot BRCA2 noncoding SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: BRCA2 SNVs with functional classifications, Huang et al. 2025 (Brixi et al. 2026)
0.54 AUROC (zero-shot; BRCA2 noncoding SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on BRCA2 noncoding SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-brca2-noncoding-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I560, row 560: Model 'RNA-FM', Data 'BRCA2', Genomic_Feature 'Noncoding', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.015 AUPRC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-low-spliceai-pangolin-scores-non-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J663, row 663: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Low SpliceAI/Pangolin scores', Variant_Type 'Non-SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.508 AUROC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar low SpliceAI and Pangolin scores (both below 0.1) non-SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-low-spliceai-pangolin-scores-non-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I663, row 663: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Low SpliceAI/Pangolin scores', Variant_Type 'Non-SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.004 AUPRC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-low-spliceai-pangolin-scores-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J675, row 675: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Low SpliceAI/Pangolin scores', Variant_Type 'SNV', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.536 AUROC (zero-shot; ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar low SpliceAI and Pangolin scores (both below 0.1) SNVs (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-low-spliceai-pangolin-scores-snv

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I675, row 675: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Low SpliceAI/Pangolin scores', Variant_Type 'SNV', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding indels classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.187 AUPRC (zero-shot; ClinVar noncoding indels)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding indels (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-indel

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J87, row 87: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'Indel', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding indels classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.513 AUROC (zero-shot; ClinVar noncoding indels)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding indels (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-indel

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I87, row 87: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'Indel', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding microsatellite variants classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.013 AUPRC (zero-shot; ClinVar noncoding microsatellite variants)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding microsatellite variants (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-microsatellite

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J115, row 115: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'Microsatellite', Sub_category '', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding microsatellite variants classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.617 AUROC (zero-shot; ClinVar noncoding microsatellite variants)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding microsatellite variants (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-microsatellite

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I115, row 115: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'Microsatellite', Sub_category '', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding non-SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.07 AUPRC (zero-shot; ClinVar noncoding non-SNVs, far from splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding non-SNVs, far from splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-non-snv-far-from-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J220, row 220: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'non-SNV', Sub_category 'Far from splice site', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding non-SNVs, far from splice site classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.51 AUROC (zero-shot; ClinVar noncoding non-SNVs, far from splice site)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding non-SNVs, far from splice site (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-non-snv-far-from-splice-site

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I220, row 220: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'non-SNV', Sub_category 'Far from splice site', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding non-SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.746 AUPRC (zero-shot; ClinVar noncoding non-SNVs, highly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding non-SNVs, highly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-non-snv-highly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J363, row 363: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'non-SNV', Sub_category 'Highly conserved', column 'AUPRC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding non-SNVs, highly conserved classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.517 AUROC (zero-shot; ClinVar noncoding non-SNVs, highly conserved)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding non-SNVs, highly conserved (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-non-snv-highly-conserved

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell I363, row 363: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'non-SNV', Sub_category 'Highly conserved', column 'AUROC'
Configuration: RNA-FM (Evo 2 paper variant effect evaluations)Protocol: Zero-shot ClinVar noncoding non-SNVs, intergenic classification (Evo 2 paper, Supplementary Data 1)
Dataset: ClinVar October 2024 release, filtered (Brixi et al. 2026)
0.71 AUPRC (zero-shot; ClinVar noncoding non-SNVs, intergenic)
unitless · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

RNA-FM on ClinVar noncoding non-SNVs, intergenic (Evo 2 paper)

gfm-guides-20261014-evo2-brixi2026-protocol-clinvar-noncoding-non-snv-intergenic

Aggregation: Not reported

Genome modelling and design across all domains of life with Evo 2: Supplementary Data 1, human variant effect prediction results (Nature 2026); Genome modelling and design across all domains of life with Evo 2: Supplementary Information (Nature 2026) · Supplementary Data 1 (sheet 'Sheet1') cell J231, row 231: Model 'RNA-FM', Data 'ClinVar', Genomic_Feature 'Noncoding', Variant_Type 'non-SNV', Sub_category 'Intergenic', column 'AUPRC'

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

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Stable ID: gfm-guides-20261014-evo2-brixi2026-config-rna-fm

areas
dna-genomes
contexts
research
method types
foundation_model
reported name
RNA-FM
foundation model eligible
true
parameters
RNA language model (reference 128); checkpoint not stated
source locator
Supplementary Data 1 column 'Model' ('RNA-FM'); SI A.3.12 (page 13)
missing metadata
access reuse: reason: unextracted; checkpoint revision: reason: unreported; version: reason: unreported; note: Checkpoint or release used for variant scoring not stated
provenance note
RNA-FM as scored zero-shot by the Evo 2 authors on human variant effect benchmarks.
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