Gene expression and splicing QTL analysis of blood cells in African American participants from the Jackson Heart Study

Author:

Wen Jia1,Sun Quan2ORCID,Huang Le3,Zhou Lingbo2,Doyle Margaret F4,Ekunwe Lynette5,Durda Peter4,Olson Nels C4,Reiner Alexander P67,Li Yun12,Raffield Laura M1ORCID

Affiliation:

1. Department of Genetics, University of North Carolina at Chapel Hill , Chapel Hill, NC 27514 , USA

2. Department of Biostatistics, University of North Carolina at Chapel Hill , Chapel Hill, NC 27599 , USA

3. Curriculum in Bioinformatics and Computational Biology, University of North Carolina at Chapel Hill , Chapel Hill, NC 27599 , USA

4. Department of Pathology and Laboratory Medicine, Larner College of Medicine, University of Vermont , Burlington, VT 05405 , USA

5. Department of Medicine, University of MS Medical Center (UMMC) , Jackson, MS 39213 , USA

6. Department of Epidemiology, University of Washington , Seattle, WA 98195 , USA

7. Division of Public Health Sciences, Fred Hutchinson Cancer Research , Seattle, WA 98109 , USA

Abstract

Abstract Most gene expression and alternative splicing quantitative trait loci (eQTL/sQTL) studies have been biased toward European ancestry individuals. Here, we performed eQTL and sQTL analyses using TOPMed whole-genome sequencing-derived genotype data and RNA-sequencing data from stored peripheral blood mononuclear cells in 1,012 African American participants from the Jackson Heart Study (JHS). At a false discovery rate of 5%, we identified 17,630 unique eQTL credible sets covering 16,538 unique genes; and 24,525 unique sQTL credible sets covering 9,605 unique genes, with lead QTL at P < 5e−8. About 24% of independent eQTLs and independent sQTLs with a minor allele frequency > 1% in JHS were rare (minor allele frequency < 0.1%), and therefore unlikely to be detected, in European ancestry individuals. Finally, we created an open database, which is freely available online, allowing fast query and bulk download of our QTL results.

Funder

National Institutes of Health

NIH

Publisher

Oxford University Press (OUP)

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