Statistical construction of calibrated prediction intervals for polygenic score-based phenotype prediction
Accurately quantifying uncertainty in predicted phenotypes from polygenic score (PGS)-based applications is essential for reliable clinical interpretation of PGS, supporting effective disease risk assessment and informed decision-making. Here, we present PredInterval, a nonparametric method for constructing well-calibrated prediction intervals. PredInterval is compatible with any PGS method, takes either individual-level data or summary statistics as input and relies on information from quantiles of phenotypic residuals through cross-validation to achieve well-calibrated coverage of true phenotypic values across diverse genetic architectures. We apply PredInterval to analyze 17 traits in real-data applications, where PredInterval not only represents the sole method achieving well-calibrated prediction coverage across traits, but it also offers a principled approach to identify high-risk individuals using prediction intervals, leading to an average improvement of identification rates by 8.7-830.4% compared with existing approaches. Overall, PredInterval represents a robust and versatile tool for enhancing the clinical utility of PGS.
Authors
- Chang Xu (ORCID: https://orcid.org/0000-0003-2831-1604)
- Xiang Zhou (ORCID: https://orcid.org/0000-0002-4331-7599)
- Santhi K. Ganesh (ORCID: https://orcid.org/0000-0002-3663-5249)
Institutions
- University of Michigan (US)
- Yale University (US)
- Michigan Medicine (US)
Publication Details
- Journal
- Nature Genetics
- Published
- 2025-10-13
- DOI
- https://doi.org/10.1038/s41588-025-02360-6
- Citations
- 2
- Primary Topic
- Genetic Associations and Epidemiology
- Type
- article
- Field-Weighted Citation Impact
- 3.63
Funders
- Wellcome Trust
- British Heart Foundation
- Diabetes UK
- Northwest Regional Development Agency
- National Institutes of Health
- Medical Research Council