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Leveraging allelic imbalance to refine fine-mapping for eQTL studies

Author

Listed:
  • Jennifer Zou
  • Farhad Hormozdiari
  • Brandon Jew
  • Stephane E Castel
  • Tuuli Lappalainen
  • Jason Ernst
  • Jae Hoon Sul
  • Eleazar Eskin

Abstract

Many disease risk loci identified in genome-wide association studies are present in non-coding regions of the genome. Previous studies have found enrichment of expression quantitative trait loci (eQTLs) in disease risk loci, indicating that identifying causal variants for gene expression is important for elucidating the genetic basis of not only gene expression but also complex traits. However, detecting causal variants is challenging due to complex genetic correlation among variants known as linkage disequilibrium (LD) and the presence of multiple causal variants within a locus. Although several fine-mapping approaches have been developed to overcome these challenges, they may produce large sets of putative causal variants when true causal variants are in high LD with many non-causal variants. In eQTL studies, there is an additional source of information that can be used to improve fine-mapping called allelic imbalance (AIM) that measures imbalance in gene expression on two chromosomes of a diploid organism. In this work, we develop a novel statistical method that leverages both AIM and total expression data to detect causal variants that regulate gene expression. We illustrate through simulations and application to 10 tissues of the Genotype-Tissue Expression (GTEx) dataset that our method identifies the true causal variants with higher specificity than an approach that uses only eQTL information. Across all tissues and genes, our method achieves a median reduction rate of 11% in the number of putative causal variants. We use chromatin state data from the Roadmap Epigenomics Consortium to show that the putative causal variants identified by our method are enriched for active regions of the genome, providing orthogonal support that our method identifies causal variants with increased specificity.Author summary: In recent years, many studies have identified genetic variants that are associated with the expression of genes (eQTLs). While thousands of eQTLs have been identified, not all associated variants cause changes in gene expression. This is in part due to the complex patterns of genetic correlation in the human genome. If a region of the genome contains many genetic variants that are highly correlated with each other, non-causal genetic variants close to a causal variant are also correlated with gene expression. Statistical fine-mapping is the process of identifying true causal variants from a set of candidate variants. In regions with high genetic correlation, previous fine-mapping methods may not be able to differentiate causal variants from nearby variants. We propose a method that utilizes a complementary source of information called allelic imbalance (AIM). We show that by combining eQTL and AIM data, we can identify the true causal variants more efficiently and substantially decrease the number of putative causal variants for downstream analysis.

Suggested Citation

  • Jennifer Zou & Farhad Hormozdiari & Brandon Jew & Stephane E Castel & Tuuli Lappalainen & Jason Ernst & Jae Hoon Sul & Eleazar Eskin, 2019. "Leveraging allelic imbalance to refine fine-mapping for eQTL studies," PLOS Genetics, Public Library of Science, vol. 15(12), pages 1-24, December.
  • Handle: RePEc:plo:pgen00:1008481
    DOI: 10.1371/journal.pgen.1008481
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    References listed on IDEAS

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    1. Yi-Juan Hu & Wei Sun & Jung-Ying Tzeng & Charles M. Perou, 2015. "Proper Use of Allele-Specific Expression Improves Statistical Power for cis -eQTL Mapping with RNA-Seq Data," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 110(511), pages 962-974, September.
    2. Bryan N Howie & Peter Donnelly & Jonathan Marchini, 2009. "A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies," PLOS Genetics, Public Library of Science, vol. 5(6), pages 1-15, June.
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