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Transethnic Genetic-Correlation Estimates from Summary Statistics

Overview
Journal Am J Hum Genet
Publisher Cell Press
Specialty Genetics
Date 2016 Jun 21
PMID 27321947
Citations 163
Authors
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Abstract

The increasing number of genetic association studies conducted in multiple populations provides an unprecedented opportunity to study how the genetic architecture of complex phenotypes varies between populations, a problem important for both medical and population genetics. Here, we have developed a method for estimating the transethnic genetic correlation: the correlation of causal-variant effect sizes at SNPs common in populations. This methods takes advantage of the entire spectrum of SNP associations and uses only summary-level data from genome-wide association studies. This avoids the computational costs and privacy concerns associated with genotype-level information while remaining scalable to hundreds of thousands of individuals and millions of SNPs. We applied our method to data on gene expression, rheumatoid arthritis, and type 2 diabetes and overwhelmingly found that the genetic correlation was significantly less than 1. Our method is implemented in a Python package called Popcorn.

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References
1.
Hormozdiari F, Kostem E, Kang E, Pasaniuc B, Eskin E . Identifying causal variants at loci with multiple signals of association. Genetics. 2014; 198(2):497-508. PMC: 4196608. DOI: 10.1534/genetics.114.167908. View

2.
Price A, Helgason A, Thorleifsson G, McCarroll S, Kong A, Stefansson K . Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals. PLoS Genet. 2011; 7(2):e1001317. PMC: 3044684. DOI: 10.1371/journal.pgen.1001317. View

3.
Chang M, Ned R, Hong Y, Yesupriya A, Yang Q, Liu T . Racial/ethnic variation in the association of lipid-related genetic variants with blood lipids in the US adult population. Circ Cardiovasc Genet. 2011; 4(5):523-33. DOI: 10.1161/CIRCGENETICS.111.959577. View

4.
Marenberg M, Risch N, Berkman L, Floderus B, de Faire U . Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med. 1994; 330(15):1041-6. DOI: 10.1056/NEJM199404143301503. View

5.
Yang J, Benyamin B, McEvoy B, Gordon S, Henders A, Nyholt D . Common SNPs explain a large proportion of the heritability for human height. Nat Genet. 2010; 42(7):565-9. PMC: 3232052. DOI: 10.1038/ng.608. View