| Literature DB >> 26747043 |
Timothy Shin Heng Mak1, Johnny Sheung Him Kwan2, Desmond Dedalus Campbell2, Pak Chung Sham3,4,5.
Abstract
A polygenic score is commonly derived using genome-wide genotype data to summarize the genetic contribution to a particular disease at the individual level. Usually it is constructed as a linear combination of SNP genotype weighted by the SNP-wise regression coefficient of the SNP to the phenotype using SNPs with p values smaller than a particular threshold. Commonly a range of thresholds are used which can pose problems with multiple comparisons as well as over-fitting. Here, an alternative weighting scheme is proposed, making use of the local true discovery rate, estimated from summary statistics. Two methods of estimation are proposed-maximum likelihood and kernel density estimation. Simulation studies using real and artificial data suggest this new weighting scheme is highly comparable with standard polygenic scores using the best possible p value threshold in prediction, even though this threshold is not normally known in practice.Entities:
Keywords: Genome wide association studies; Local false discovery rate; Polygenic score; Risk prediction
Mesh:
Year: 2016 PMID: 26747043 DOI: 10.1007/s10519-015-9770-2
Source DB: PubMed Journal: Behav Genet ISSN: 0001-8244 Impact factor: 2.805