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The impact of non-additive genetic associations on age-related complex diseases
Genome-wide association studies (GWAS) are not fully comprehensive, as current strategies typically test only the additive model, exclude the X chromosome, and use only one reference panel for genotype imputation. We implement an extensive GWAS strategy, GUIDANCE, which improves genotype imputation...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065056/ https://www.ncbi.nlm.nih.gov/pubmed/33893285 http://dx.doi.org/10.1038/s41467-021-21952-4 |
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author | Guindo-Martínez, Marta Amela, Ramon Bonàs-Guarch, Silvia Puiggròs, Montserrat Salvoro, Cecilia Miguel-Escalada, Irene Carey, Caitlin E. Cole, Joanne B. Rüeger, Sina Atkinson, Elizabeth Leong, Aaron Sanchez, Friman Ramon-Cortes, Cristian Ejarque, Jorge Palmer, Duncan S. Kurki, Mitja Aragam, Krishna Florez, Jose C. Badia, Rosa M. Mercader, Josep M. Torrents, David |
author_facet | Guindo-Martínez, Marta Amela, Ramon Bonàs-Guarch, Silvia Puiggròs, Montserrat Salvoro, Cecilia Miguel-Escalada, Irene Carey, Caitlin E. Cole, Joanne B. Rüeger, Sina Atkinson, Elizabeth Leong, Aaron Sanchez, Friman Ramon-Cortes, Cristian Ejarque, Jorge Palmer, Duncan S. Kurki, Mitja Aragam, Krishna Florez, Jose C. Badia, Rosa M. Mercader, Josep M. Torrents, David |
author_sort | Guindo-Martínez, Marta |
collection | PubMed |
description | Genome-wide association studies (GWAS) are not fully comprehensive, as current strategies typically test only the additive model, exclude the X chromosome, and use only one reference panel for genotype imputation. We implement an extensive GWAS strategy, GUIDANCE, which improves genotype imputation by using multiple reference panels and includes the analysis of the X chromosome and non-additive models to test for association. We apply this methodology to 62,281 subjects across 22 age-related diseases and identify 94 genome-wide associated loci, including 26 previously unreported. Moreover, we observe that 27.7% of the 94 loci are missed if we use standard imputation strategies with a single reference panel, such as HRC, and only test the additive model. Among the new findings, we identify three novel low-frequency recessive variants with odds ratios larger than 4, which need at least a three-fold larger sample size to be detected under the additive model. This study highlights the benefits of applying innovative strategies to better uncover the genetic architecture of complex diseases. |
format | Online Article Text |
id | pubmed-8065056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80650562021-05-11 The impact of non-additive genetic associations on age-related complex diseases Guindo-Martínez, Marta Amela, Ramon Bonàs-Guarch, Silvia Puiggròs, Montserrat Salvoro, Cecilia Miguel-Escalada, Irene Carey, Caitlin E. Cole, Joanne B. Rüeger, Sina Atkinson, Elizabeth Leong, Aaron Sanchez, Friman Ramon-Cortes, Cristian Ejarque, Jorge Palmer, Duncan S. Kurki, Mitja Aragam, Krishna Florez, Jose C. Badia, Rosa M. Mercader, Josep M. Torrents, David Nat Commun Article Genome-wide association studies (GWAS) are not fully comprehensive, as current strategies typically test only the additive model, exclude the X chromosome, and use only one reference panel for genotype imputation. We implement an extensive GWAS strategy, GUIDANCE, which improves genotype imputation by using multiple reference panels and includes the analysis of the X chromosome and non-additive models to test for association. We apply this methodology to 62,281 subjects across 22 age-related diseases and identify 94 genome-wide associated loci, including 26 previously unreported. Moreover, we observe that 27.7% of the 94 loci are missed if we use standard imputation strategies with a single reference panel, such as HRC, and only test the additive model. Among the new findings, we identify three novel low-frequency recessive variants with odds ratios larger than 4, which need at least a three-fold larger sample size to be detected under the additive model. This study highlights the benefits of applying innovative strategies to better uncover the genetic architecture of complex diseases. Nature Publishing Group UK 2021-04-23 /pmc/articles/PMC8065056/ /pubmed/33893285 http://dx.doi.org/10.1038/s41467-021-21952-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Guindo-Martínez, Marta Amela, Ramon Bonàs-Guarch, Silvia Puiggròs, Montserrat Salvoro, Cecilia Miguel-Escalada, Irene Carey, Caitlin E. Cole, Joanne B. Rüeger, Sina Atkinson, Elizabeth Leong, Aaron Sanchez, Friman Ramon-Cortes, Cristian Ejarque, Jorge Palmer, Duncan S. Kurki, Mitja Aragam, Krishna Florez, Jose C. Badia, Rosa M. Mercader, Josep M. Torrents, David The impact of non-additive genetic associations on age-related complex diseases |
title | The impact of non-additive genetic associations on age-related complex diseases |
title_full | The impact of non-additive genetic associations on age-related complex diseases |
title_fullStr | The impact of non-additive genetic associations on age-related complex diseases |
title_full_unstemmed | The impact of non-additive genetic associations on age-related complex diseases |
title_short | The impact of non-additive genetic associations on age-related complex diseases |
title_sort | impact of non-additive genetic associations on age-related complex diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065056/ https://www.ncbi.nlm.nih.gov/pubmed/33893285 http://dx.doi.org/10.1038/s41467-021-21952-4 |
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