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Uncovering Causal Gene-tissue Pairs and Variants: A Multivariable TWAS Method Controlling for Infinitesimal Effects

Overview
Journal Res Sq
Date 2024 Dec 23
PMID 39711576
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Abstract

Transcriptome-wide association studies (TWAS) are commonly used to prioritize causal genes underlying associations found in genome-wide association studies (GWAS) and have been extended to identify causal genes through multivariable TWAS methods. However, recent studies have shown that widespread infinitesimal effects due to polygenicity can impair the performance of these methods. In this report, we introduce a multivariable TWAS method named Tissue-Gene pairs, direct causal Variants, and Infinitesimal effects selector (TGVIS) to identify tissue-specific causal genes and direct causal variants while accounting for infinitesimal effects. In simulations, TGVIS maintains an accurate prioritization of causal gene-tissue pairs and variants and demonstrates comparable or superior power to existing approaches, regardless of the presence of infinitesimal effects. In the real data analysis of GWAS summary data of 45 cardiometabolic traits and expression/splicing quantitative trait loci (eQTL/sQTL) from 31 tissues, TGVIS improves causal gene prioritization and enhances the biological interpretability over existing methods.

References
1.
Benner C, Spencer C, Havulinna A, Salomaa V, Ripatti S, Pirinen M . FINEMAP: efficient variable selection using summary data from genome-wide association studies. Bioinformatics. 2016; 32(10):1493-501. PMC: 4866522. DOI: 10.1093/bioinformatics/btw018. View

2.
Vinuela A, Varshney A, van de Bunt M, Prasad R, Asplund O, Bennett A . Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D. Nat Commun. 2020; 11(1):4912. PMC: 7528108. DOI: 10.1038/s41467-020-18581-8. View

3.
Suzuki K, Hatzikotoulas K, Southam L, Taylor H, Yin X, Lorenz K . Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. 2024; 627(8003):347-357. PMC: 10937372. DOI: 10.1038/s41586-024-07019-6. View

4.
Kirk T, Ahmed A, Rognoni E . Fibroblast Memory in Development, Homeostasis and Disease. Cells. 2021; 10(11). PMC: 8616330. DOI: 10.3390/cells10112840. View

5.
Wittich H, Ardlie K, Taylor K, Durda P, Liu Y, Mikhaylova A . Transcriptome-wide association study of the plasma proteome reveals cis and trans regulatory mechanisms underlying complex traits. Am J Hum Genet. 2024; 111(3):445-455. PMC: 10940016. DOI: 10.1016/j.ajhg.2024.01.006. View