Publication
Title
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
Author
Institution/Organisation
Schizophrenia Working Group of the Psychiatric Genomics Consortium
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) Study
Abstract
Polygenic risk scores have shown great promise in predicting complex disease risk and will become more accurate as training sample sizes increase. The standard approach for calculating risk scores involves linkage disequilibrium (LD)-based marker pruning and applying a p value threshold to association statistics, but this discards information and can reduce predictive accuracy. We introduce LDpred, a method that infers the posterior mean effect size of each marker by using a prior on effect sizes and LD information from an external reference panel. Theory and simulations show that LDpred outperforms the approach of pruning followed by thresholding, particularly at large sample sizes. Accordingly, predicted R2 increased from 20.1% to 25.3% in a large schizophrenia dataset and from 9.8% to 12.0% in a large multiple sclerosis dataset. A similar relative improvement in accuracy was observed for three additional large disease datasets and for non-European schizophrenia samples. The advantage of LDpred over existing methods will grow as sample sizes increase.
Language
English
Source (journal)
The American journal of human genetics / American Society of Human Genetics [Bethesda, Md] - New York, N.Y., 1949, currens
Publication
New York, N.Y. : 2015
ISSN
0002-9297 [print]
1537-6605 [online]
DOI
10.1016/J.AJHG.2015.09.001
Volume/pages
97 :4 (2015) , p. 576-592
ISI
000362617300008
Full text (Publisher's DOI)
Full text (publisher's version - intranet only)
UAntwerpen
Faculty/Department
Research group
Project info
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Subject
External links
Web of Science
Record
Identifier
Creation 01.12.2016
Last edited 28.01.2023
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