Expanding the utility of variant effect predictions with phenotype-specific models

Current methods for variant effect prediction do not differentiate between pathogenic variants resulting in different disease outcomes and are restricted in application due to a focus on variants with a single molecular consequence. We have developed Variant-to-Phenotype (V2P), a multi-task, multi-output machine learning model to predict variant pathogenicity conditioned on top-level Human Phenotype Ontology disease phenotypes (n = 23) for single nucleotide variants and insertions/deletions throughout the human genome. V2P leverages a unique approach for the modeling of variant effect that incorporates resultant disease phenotypes as output and during training to improve the quality of variant disease phenotype and effect predictions, simultaneously. We describe the architecture, training strategy, and biological features contributing to V2P's output, revealing initial characteristics underlying the relationship between disease genotype and phenotype. Moreover, we demonstrate the benefit of incorporating disease phenotypes for variant effect predictions by comparing V2P with several variant effect predictors across various high-quality evaluation datasets from manually curated databases and functional assays. Finally, we examine how V2P's predictions result in the successful identification of pathogenic variants in real and simulated patient sequencing data, outperforming other tested methods in initial comparisons. V2P offers a complete mapping of human genetic variants to disease-phenotypes, offering a uniquely conditioned set of variant effect characterizations.

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Publication Details

Journal
Nature Communications
Published
2025-11-28
DOI
https://doi.org/10.1038/s41467-025-66607-w
Citations
1
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
1.82

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article

Expanding the utility of variant effect predictions with phenotype-specific models

Bertrand Boisson, Yuval Itan, Matthew Mort, D.N. Cooper et al.
1 citations
Nature Communications
Genomics and Rare Diseases
1.82
article

Expanding the utility of variant effect predictions with phenotype-specific models

Bertrand Boisson, Yuval Itan, Matthew Mort, D.N. Cooper, Meltem Ece Kars, Jean‐Laurent Casanova, Avner Schlessinger, Baptiste Milisavljevic, Peter D. Stenson, David Stein, Peng Zhang
article en
1 citations

Abstract

Current methods for variant effect prediction do not differentiate between pathogenic variants resulting in different disease outcomes and are restricted in application due to a focus on variants with a single molecular consequence. We have developed Variant-to-Phenotype (V2P), a multi-task, multi-output machine learning model to predict variant pathogenicity conditioned on top-level Human Phenotype Ontology disease phenotypes (n = 23) for single nucleotide variants and insertions/deletions throughout the human genome. V2P leverages a unique approach for the modeling of variant effect that incorporates resultant disease phenotypes as output and during training to improve the quality of variant disease phenotype and effect predictions, simultaneously. We describe the architecture, training strategy, and biological features contributing to V2P's output, revealing initial characteristics underlying the relationship between disease genotype and phenotype. Moreover, we demonstrate the benefit of incorporating disease phenotypes for variant effect predictions by comparing V2P with several variant effect predictors across various high-quality evaluation datasets from manually curated databases and functional assays. Finally, we examine how V2P's predictions result in the successful identification of pathogenic variants in real and simulated patient sequencing data, outperforming other tested methods in initial comparisons. V2P offers a complete mapping of human genetic variants to disease-phenotypes, offering a uniquely conditioned set of variant effect characterizations.

Nature CommunicationsVol. 16(1)
Howard Hughes Medical Institute (US), Inserm (FR), Université Paris Cité (FR), Child Health and Development Institute (US), Human Genetic of Infectious Diseases (FR), Institut des Maladies Génétiques Imagine (FR), Cardiff University (GB), Rockefeller University (US), Icahn School of Medicine at Mount Sinai (US)
St. Giles Foundation, Leona M. and Harry B. Helmsley Charitable Trust, Fondation du Souffle, Georgia Clinical and Translational Science Alliance, Institut des maladies génétiques Imagine, Cardiff University, Agence Nationale de la Recherche, Fondation Leducq, Institut National de la Santé et de la Recherche Médicale, Fondation pour la Recherche Médicale, National Institutes of Health, National Center for Advancing Translational Sciences
Openalex Percentile: Top 11%
Genomics and Rare Diseases
1.82
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