LDpred2: better, faster, stronger

Author:

Privé Florian1,Arbel Julyan2,Vilhjálmsson Bjarni J13

Affiliation:

1. National Centre for Register-Based Research, Aarhus University, Aarhus 8210, Denmark

2. Univ. Grenoble Alpes, Inria, CNRS, Grenoble INP, LJK, Grenoble 38000, France

3. Bioinformatics Research Centre, Aarhus University, Aarhus 8000, Denmark

Abstract

Abstract Motivation Polygenic scores have become a central tool in human genetics research. LDpred is a popular method for deriving polygenic scores based on summary statistics and a matrix of correlation between genetic variants. However, LDpred has limitations that may reduce its predictive performance. Results Here, we present LDpred2, a new version of LDpred that addresses these issues. We also provide two new options in LDpred2: a ‘sparse’ option that can learn effects that are exactly 0, and an ‘auto’ option that directly learns the two LDpred parameters from data. We benchmark predictive performance of LDpred2 against the previous version on simulated and real data, demonstrating substantial improvements in robustness and predictive accuracy compared to LDpred1. We then show that LDpred2 also outperforms other polygenic score methods recently developed, with a mean AUC over the 8 real traits analyzed here of 65.1%, compared to 63.8% for lassosum, 62.9% for PRS-CS and 61.5% for SBayesR. Note that LDpred2 provides more accurate polygenic scores when run genome-wide, instead of per chromosome. Availability and implementation LDpred2 is implemented in R package bigsnpr. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Danish National Research Foundation

Lundbeck Foundation Initiative for Integrative Psychiatric Research

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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