Evidence map›Paper›PMID 37398263›Full record

ArticleResearch square2023

Tuning Parameters for Polygenic Risk Score Methods Using GWAS Summary Statistics from Training Data.

Wei Jiang, Ling Chen, Matthew J Girgenti, Hongyu Zhao

Abstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Wei JiangDepartment of Biostatistics, Yale School of Public Health, New Haven, CT, USA.ORCID 0000-0001-6120-5278
Ling ChenDepartment of Statistics, Columbia University, New York, NY, USA.
Matthew J GirgentiDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0003-1647-326X
Hongyu ZhaoDepartment of Biostatistics, Yale School of Public Health, New Haven, CT, USA.ORCID 0000-0003-1195-9607

Funding

Statistical Methods for Genetic Risk Predictions across Diverse PopulationsR01HG012735 · NHGRI · YALE UNIVERSITY · PI ZHAO, HONGYU · 2022 to 2025
$2.4M
Novel statistical methods and tools to integrate multiple endophenotypes and functional annotation data to study the roles of rare variants in complex human diseases using sequencing dataR01GM134005 · NIGMS · YALE UNIVERSITY · PI WU, BAOLIN, ZHAO, HONGYU · 2020 to 2023
$1.6M
NHGRI NIH HHS R01 HG012735NIGMS NIH HHS R01 GM134005
6 · The paper itself

Abstract

Predicting genetic risks for common diseases may improve their prevention and early treatment. In recent years, various additive-model-based polygenic risk scores (PRS) methods have been proposed to combine the estimated effects of single nucleotide polymorphisms (SNPs) using data collected from genome-wide association studies (GWAS). Some of these methods require access to another external individual-level GWAS dataset to tune the hyperparameters, which can be difficult because of privacy and security-related concerns. Additionally, leaving out partial data for hyperparameter tuning can reduce the predictive accuracy of the constructed PRS model. In this article, we propose a novel method, called PRStuning, to automatically tune hyperparameters for different PRS methods using only GWAS summary statistics from the training data. The core idea is to first predict the performance of the PRS method with different parameter values, and then select the parameters with the best prediction performance. Because directly using the effects observed from the training data tends to overestimate the performance in the testing data (a phenomenon known as overfitting), we adopt an empirical Bayes approach to shrinking the predicted performance in accordance with the estimated genetic architecture of the disease. Results from extensive simulations and real data applications demonstrate that PRStuning can accurately predict the PRS performance across PRS methods and parameters, and it can help select the best-performing parameters.

Identifiers

PMID37398263
PMCPMC10312948

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.