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Accurate prediction of an individual's phenotype from their DNA sequence is one of the great promises of genomics and precision medicine. We extend a powerful individual-level data Bayesian multiple regression model (BayesR) to one that utilises summary statistics from genome-wide association studies (GWAS), SBayesR. In simulation and cross-validation using 12 real traits and 1.1 million variants on 350,000 individuals from the UK Biobank, SBayesR improves prediction accuracy relative to commonly used state-of-the-art summary statistics methods at a fraction of the computational resources. Furthermore, using summary statistics for variants from the largest GWAS meta-analysis (n ≈ 700, 000) on height and BMI, we show that on average across traits and two independent data sets that SBayesR improves prediction R2 by 5.2% relative to LDpred and by 26.5% relative to clumping and p value thresholding.

Original publication

DOI

10.1038/s41467-019-12653-0

Type

Journal article

Journal

Nature communications

Publication Date

11/2019

Volume

10

Addresses

Institute for Molecular Bioscience, University of Queensland, St Lucia, Brisbane, 4072, QLD, Australia. luke.lloydjones@uqconnect.edu.au.

Keywords

Adipose Tissue, Humans, Alopecia, Diabetes Mellitus, Type 2, Birth Weight, Basal Metabolism, Vital Capacity, Forced Expiratory Volume, Body Mass Index, Body Height, Waist-Hip Ratio, Bayes Theorem, Regression Analysis, Body Composition, Bone Density, Multifactorial Inheritance, Polymorphism, Single Nucleotide, Biological Specimen Banks, Statistics as Topic, Genome-Wide Association Study, Genetic Association Studies