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Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression
Genetic association signals have been mostly found in noncoding regions through genome-wide association studies (GWAS), suggesting the roles of gene expression regulation in human diseases and traits. However, there has been limited success in colocalizing expression quantitative trait locus (eQTL)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599978/ https://www.ncbi.nlm.nih.gov/pubmed/37901453 http://dx.doi.org/10.1093/biomethods/bpad024 |
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author | Lin, Chen Liu, Wei Jiang, Wei Zhao, Hongyu |
author_facet | Lin, Chen Liu, Wei Jiang, Wei Zhao, Hongyu |
author_sort | Lin, Chen |
collection | PubMed |
description | Genetic association signals have been mostly found in noncoding regions through genome-wide association studies (GWAS), suggesting the roles of gene expression regulation in human diseases and traits. However, there has been limited success in colocalizing expression quantitative trait locus (eQTL) with disease-associated variants. Mediated expression score regression (MESC) is a recently proposed method to quantify the proportion of trait heritability mediated by genetically regulated gene expressions (GReX). Applications of MESC to GWAS results have yielded low estimation of mediated heritability for many traits. As MESC relies on stringent independence assumptions between cis-eQTL effects, gene effects, and nonmediated SNP effects, it may fail to characterize the true relationships between those effect sizes, which leads to biased results. Here, we consider the robustness of MESC to investigate whether the low fraction of mediated heritability inferred by MESC reflects biological reality for complex traits or is an underestimation caused by model misspecifications. Our results suggest that MESC may lead to biased estimates of mediated heritability with misspecification of gene annotations leading to underestimation, whereas misspecification of SNP annotations may lead to overestimation. Furthermore, errors in eQTL effect estimates may lead to underestimation of mediated heritability. |
format | Online Article Text |
id | pubmed-10599978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105999782023-10-27 Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression Lin, Chen Liu, Wei Jiang, Wei Zhao, Hongyu Biol Methods Protoc Review Genetic association signals have been mostly found in noncoding regions through genome-wide association studies (GWAS), suggesting the roles of gene expression regulation in human diseases and traits. However, there has been limited success in colocalizing expression quantitative trait locus (eQTL) with disease-associated variants. Mediated expression score regression (MESC) is a recently proposed method to quantify the proportion of trait heritability mediated by genetically regulated gene expressions (GReX). Applications of MESC to GWAS results have yielded low estimation of mediated heritability for many traits. As MESC relies on stringent independence assumptions between cis-eQTL effects, gene effects, and nonmediated SNP effects, it may fail to characterize the true relationships between those effect sizes, which leads to biased results. Here, we consider the robustness of MESC to investigate whether the low fraction of mediated heritability inferred by MESC reflects biological reality for complex traits or is an underestimation caused by model misspecifications. Our results suggest that MESC may lead to biased estimates of mediated heritability with misspecification of gene annotations leading to underestimation, whereas misspecification of SNP annotations may lead to overestimation. Furthermore, errors in eQTL effect estimates may lead to underestimation of mediated heritability. Oxford University Press 2023-10-17 /pmc/articles/PMC10599978/ /pubmed/37901453 http://dx.doi.org/10.1093/biomethods/bpad024 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Review Lin, Chen Liu, Wei Jiang, Wei Zhao, Hongyu Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
title | Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
title_full | Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
title_fullStr | Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
title_full_unstemmed | Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
title_short | Robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
title_sort | robustness of quantifying mediating effects of genetically regulated expression on complex traits with mediated expression score regression |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599978/ https://www.ncbi.nlm.nih.gov/pubmed/37901453 http://dx.doi.org/10.1093/biomethods/bpad024 |
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