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A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease
Background: Genome-wide association studies have successfully identified variants associated with multiple conditions. However, generalizing discoveries across diverse populations remains challenging due to large variations in genetic composition. Methods that perform gene expression imputation have...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319087/ https://www.ncbi.nlm.nih.gov/pubmed/35883662 http://dx.doi.org/10.3390/cells11142219 |
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author | Dai, Yulin Jia, Peilin Zhao, Zhongming Gottlieb, Assaf |
author_facet | Dai, Yulin Jia, Peilin Zhao, Zhongming Gottlieb, Assaf |
author_sort | Dai, Yulin |
collection | PubMed |
description | Background: Genome-wide association studies have successfully identified variants associated with multiple conditions. However, generalizing discoveries across diverse populations remains challenging due to large variations in genetic composition. Methods that perform gene expression imputation have attempted to address the transferability of gene discoveries across populations, but with limited success. Methods: Here, we introduce a pipeline that combines gene expression imputation with gene module discovery, including a dense gene module search and a gene set variation analysis, to address the transferability issue. Our method feeds association probabilities of imputed gene expression with a selected phenotype into tissue-specific gene-module discovery over protein interaction networks to create higher-level gene modules. Results: We demonstrate our method’s utility in three case-control studies of Alzheimer’s disease (AD) for three different race/ethnic populations (Whites, African descent and Hispanics). We discovered 182 AD-associated genes from gene modules shared between these populations, highlighting new gene modules associated with AD. Conclusions: Our innovative framework has the potential to identify robust discoveries across populations based on gene modules, as demonstrated in AD. |
format | Online Article Text |
id | pubmed-9319087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93190872022-07-27 A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease Dai, Yulin Jia, Peilin Zhao, Zhongming Gottlieb, Assaf Cells Article Background: Genome-wide association studies have successfully identified variants associated with multiple conditions. However, generalizing discoveries across diverse populations remains challenging due to large variations in genetic composition. Methods that perform gene expression imputation have attempted to address the transferability of gene discoveries across populations, but with limited success. Methods: Here, we introduce a pipeline that combines gene expression imputation with gene module discovery, including a dense gene module search and a gene set variation analysis, to address the transferability issue. Our method feeds association probabilities of imputed gene expression with a selected phenotype into tissue-specific gene-module discovery over protein interaction networks to create higher-level gene modules. Results: We demonstrate our method’s utility in three case-control studies of Alzheimer’s disease (AD) for three different race/ethnic populations (Whites, African descent and Hispanics). We discovered 182 AD-associated genes from gene modules shared between these populations, highlighting new gene modules associated with AD. Conclusions: Our innovative framework has the potential to identify robust discoveries across populations based on gene modules, as demonstrated in AD. MDPI 2022-07-16 /pmc/articles/PMC9319087/ /pubmed/35883662 http://dx.doi.org/10.3390/cells11142219 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dai, Yulin Jia, Peilin Zhao, Zhongming Gottlieb, Assaf A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease |
title | A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease |
title_full | A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease |
title_fullStr | A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease |
title_full_unstemmed | A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease |
title_short | A Method for Bridging Population-Specific Genotypes to Detect Gene Modules Associated with Alzheimer’s Disease |
title_sort | method for bridging population-specific genotypes to detect gene modules associated with alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319087/ https://www.ncbi.nlm.nih.gov/pubmed/35883662 http://dx.doi.org/10.3390/cells11142219 |
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