rewirebio.iobenchmarks
Configuration

PhyloP 100-way vertebrate (Lu et al. 2025)

PhyloP conservation score from the 100-way vertebrate alignment on GRCh38, from the UCSC Genome Browser.

14 evaluations · 14 results4 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

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)
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: 3' UTR (Figure 1)0.862Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: All variants (Figure 1)Not reportedNot reported0.908Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Intron (Non-splice) (Figure 1)Not reportedNot reportedNot reported0.852Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Missense & Intron (Non-splice) (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reported0.868Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Missense & 3'UTR (Figure 1)Not reportedNot reportedNot reportedNot reported0.853Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Missense (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reported0.856Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Noncoding (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.976Not reportedNot reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: RNA gene (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.882Not reportedNot reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Splice (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.727Not reportedNot reportedNot reportedNot reported
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: Start loss (Figure 1)Not reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reportedNot reported0.675Not reportedNot reportedNot reported
PhyloP 100-way vertebrate (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 reported0.704Not reportedNot reported
PhyloP 100-way vertebrate (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 reported0.796Not reported
PhyloP 100-way vertebrate (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 reported0.855
PhyloP 100-way vertebrate (Lu et al. 2025)EvaluationLu et al. 2025 ClinVar benchmark: 5' UTR (Figure 1)Not reported0.696Not 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: PhyloP 100-way vertebrate (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)
0.908 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.852 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.868 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.853 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.856 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.976 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.882 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.727 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.675 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.704 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.796 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.855 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.862 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

PhyloP 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 'PhyloP', bar label
Configuration: PhyloP 100-way vertebrate (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)
0.696 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

PhyloP 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 'PhyloP', bar label

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

Use this configuration

How it works, versions and access

Additional methodological details, versions and access terms have not yet been extracted into a structured profile for this configuration. Consult the linked sources and evaluation records below.

Evidence

Source checking verifies the cited claim or transcription. It does not establish independent reproduction.

Evidence table

Inspect claims, sources and review details

Trace each statement to its source and review. A context-only reference supports the record generally; it does not verify an individual field. Source checking does not reproduce an experiment.

One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.

0 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-11-02-a7f03c9e55a5
Property and statementOriginal source and locationReview and provenance

No evidence rows match these filters. Choose another scope or clear the search.

Sources and history

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

1 source record and release historyDownload this release (gzip)
Technical metadata and extraction receipts

Stable ID: lu-hetero-20261019-config-phylop-100way

areas
dna-genomes
contexts
clinical_research
method types
conventional_pipeline
reported name
PhyloP
parameters
UCSC hg38 phyloP100way precomputed scores.
source locator
Methods 'PhyloP' (page 16)
Related records

Suggest a correction