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SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data
The explosion of biobank data offers unprecedented opportunities for gene-environment interaction (GxE) studies of complex diseases because of the large sample sizes and the rich collection in genetic and non-genetic information. However, the extremely large sample size also introduces new computati...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593472/ https://www.ncbi.nlm.nih.gov/pubmed/34795690 http://dx.doi.org/10.3389/fgene.2021.710055 |
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author | Chi, Jocelyn T. Ipsen, Ilse C. F. Hsiao, Tzu-Hung Lin, Ching-Heng Wang, Li-San Lee, Wan-Ping Lu, Tzu-Pin Tzeng, Jung-Ying |
author_facet | Chi, Jocelyn T. Ipsen, Ilse C. F. Hsiao, Tzu-Hung Lin, Ching-Heng Wang, Li-San Lee, Wan-Ping Lu, Tzu-Pin Tzeng, Jung-Ying |
author_sort | Chi, Jocelyn T. |
collection | PubMed |
description | The explosion of biobank data offers unprecedented opportunities for gene-environment interaction (GxE) studies of complex diseases because of the large sample sizes and the rich collection in genetic and non-genetic information. However, the extremely large sample size also introduces new computational challenges in G×E assessment, especially for set-based G×E variance component (VC) tests, which are a widely used strategy to boost overall G×E signals and to evaluate the joint G×E effect of multiple variants from a biologically meaningful unit (e.g., gene). In this work, we focus on continuous traits and present SEAGLE, a Scalable Exact AlGorithm for Large-scale set-based G×E tests, to permit G×E VC tests for biobank-scale data. SEAGLE employs modern matrix computations to calculate the test statistic and p-value of the GxE VC test in a computationally efficient fashion, without imposing additional assumptions or relying on approximations. SEAGLE can easily accommodate sample sizes in the order of 10(5), is implementable on standard laptops, and does not require specialized computing equipment. We demonstrate the performance of SEAGLE using extensive simulations. We illustrate its utility by conducting genome-wide gene-based G×E analysis on the Taiwan Biobank data to explore the interaction of gene and physical activity status on body mass index. |
format | Online Article Text |
id | pubmed-8593472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85934722021-11-17 SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data Chi, Jocelyn T. Ipsen, Ilse C. F. Hsiao, Tzu-Hung Lin, Ching-Heng Wang, Li-San Lee, Wan-Ping Lu, Tzu-Pin Tzeng, Jung-Ying Front Genet Genetics The explosion of biobank data offers unprecedented opportunities for gene-environment interaction (GxE) studies of complex diseases because of the large sample sizes and the rich collection in genetic and non-genetic information. However, the extremely large sample size also introduces new computational challenges in G×E assessment, especially for set-based G×E variance component (VC) tests, which are a widely used strategy to boost overall G×E signals and to evaluate the joint G×E effect of multiple variants from a biologically meaningful unit (e.g., gene). In this work, we focus on continuous traits and present SEAGLE, a Scalable Exact AlGorithm for Large-scale set-based G×E tests, to permit G×E VC tests for biobank-scale data. SEAGLE employs modern matrix computations to calculate the test statistic and p-value of the GxE VC test in a computationally efficient fashion, without imposing additional assumptions or relying on approximations. SEAGLE can easily accommodate sample sizes in the order of 10(5), is implementable on standard laptops, and does not require specialized computing equipment. We demonstrate the performance of SEAGLE using extensive simulations. We illustrate its utility by conducting genome-wide gene-based G×E analysis on the Taiwan Biobank data to explore the interaction of gene and physical activity status on body mass index. Frontiers Media S.A. 2021-11-02 /pmc/articles/PMC8593472/ /pubmed/34795690 http://dx.doi.org/10.3389/fgene.2021.710055 Text en Copyright © 2021 Chi, Ipsen, Hsiao, Lin, Wang, Lee, Lu and Tzeng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Chi, Jocelyn T. Ipsen, Ilse C. F. Hsiao, Tzu-Hung Lin, Ching-Heng Wang, Li-San Lee, Wan-Ping Lu, Tzu-Pin Tzeng, Jung-Ying SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data |
title | SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data |
title_full | SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data |
title_fullStr | SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data |
title_full_unstemmed | SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data |
title_short | SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data |
title_sort | seagle: a scalable exact algorithm for large-scale set-based gene-environment interaction tests in biobank data |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593472/ https://www.ncbi.nlm.nih.gov/pubmed/34795690 http://dx.doi.org/10.3389/fgene.2021.710055 |
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