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Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability
Since the first Genome-Wide Association Studies (GWAS), thousands of variant-trait associations have been discovered. However, the sample size required to detect additional variants using standard univariate association screening is increasingly prohibitive. Multi-trait GWAS offers a relevant altern...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634875/ https://www.ncbi.nlm.nih.gov/pubmed/37961722 http://dx.doi.org/10.1101/2023.10.27.564319 |
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author | Suzuki, Yuka Ménager, Hervé Brancotte, Bryan Vernet, Raphaël Nerin, Cyril Boetto, Christophe Auvergne, Antoine Linhard, Christophe Torchet, Rachel Lechat, Pierre Troubat, Lucie Cho, Michael H. Bouzigon, Emmanuelle Aschard, Hugues Julienne, Hanna |
author_facet | Suzuki, Yuka Ménager, Hervé Brancotte, Bryan Vernet, Raphaël Nerin, Cyril Boetto, Christophe Auvergne, Antoine Linhard, Christophe Torchet, Rachel Lechat, Pierre Troubat, Lucie Cho, Michael H. Bouzigon, Emmanuelle Aschard, Hugues Julienne, Hanna |
author_sort | Suzuki, Yuka |
collection | PubMed |
description | Since the first Genome-Wide Association Studies (GWAS), thousands of variant-trait associations have been discovered. However, the sample size required to detect additional variants using standard univariate association screening is increasingly prohibitive. Multi-trait GWAS offers a relevant alternative: it can improve statistical power and lead to new insights about gene function and the joint genetic architecture of human phenotypes. Although many methodological hurdles of multi-trait testing have been discussed, the strategy to select trait, among overwhelming possibilities, has been overlooked. In this study, we conducted extensive multi-trait tests using JASS (Joint Analysis of Summary Statistics) and assessed which genetic features of the analysed sets were associated with an increased detection of variants as compared to univariate screening. Our analyses identified multiple factors associated with the gain in the association detection in multi-trait tests. Together, these factors of the analysed sets are predictive of the gain of the multi-trait test (Pearson’s [Formula: see text] equal to 0.43 between the observed and predicted gain, P < 1.6 × 10(−60)). Applying an alternative multi-trait approach (MTAG, multi-trait analysis of GWAS), we found that in most scenarios but particularly those with larger numbers of traits, JASS outperformed MTAG. Finally, we benchmark several strategies to select set of traits including the prevalent strategy of selecting clinically similar traits, which systematically underperformed selecting clinically heterogenous traits or selecting sets that issued from our data-driven models. This work provides a unique picture of the determinant of multi-trait GWAS statistical power and outline practical strategies for multi-trait testing. |
format | Online Article Text |
id | pubmed-10634875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106348752023-11-13 Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability Suzuki, Yuka Ménager, Hervé Brancotte, Bryan Vernet, Raphaël Nerin, Cyril Boetto, Christophe Auvergne, Antoine Linhard, Christophe Torchet, Rachel Lechat, Pierre Troubat, Lucie Cho, Michael H. Bouzigon, Emmanuelle Aschard, Hugues Julienne, Hanna bioRxiv Article Since the first Genome-Wide Association Studies (GWAS), thousands of variant-trait associations have been discovered. However, the sample size required to detect additional variants using standard univariate association screening is increasingly prohibitive. Multi-trait GWAS offers a relevant alternative: it can improve statistical power and lead to new insights about gene function and the joint genetic architecture of human phenotypes. Although many methodological hurdles of multi-trait testing have been discussed, the strategy to select trait, among overwhelming possibilities, has been overlooked. In this study, we conducted extensive multi-trait tests using JASS (Joint Analysis of Summary Statistics) and assessed which genetic features of the analysed sets were associated with an increased detection of variants as compared to univariate screening. Our analyses identified multiple factors associated with the gain in the association detection in multi-trait tests. Together, these factors of the analysed sets are predictive of the gain of the multi-trait test (Pearson’s [Formula: see text] equal to 0.43 between the observed and predicted gain, P < 1.6 × 10(−60)). Applying an alternative multi-trait approach (MTAG, multi-trait analysis of GWAS), we found that in most scenarios but particularly those with larger numbers of traits, JASS outperformed MTAG. Finally, we benchmark several strategies to select set of traits including the prevalent strategy of selecting clinically similar traits, which systematically underperformed selecting clinically heterogenous traits or selecting sets that issued from our data-driven models. This work provides a unique picture of the determinant of multi-trait GWAS statistical power and outline practical strategies for multi-trait testing. Cold Spring Harbor Laboratory 2023-10-27 /pmc/articles/PMC10634875/ /pubmed/37961722 http://dx.doi.org/10.1101/2023.10.27.564319 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Suzuki, Yuka Ménager, Hervé Brancotte, Bryan Vernet, Raphaël Nerin, Cyril Boetto, Christophe Auvergne, Antoine Linhard, Christophe Torchet, Rachel Lechat, Pierre Troubat, Lucie Cho, Michael H. Bouzigon, Emmanuelle Aschard, Hugues Julienne, Hanna Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability |
title | Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability |
title_full | Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability |
title_fullStr | Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability |
title_full_unstemmed | Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability |
title_short | Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability |
title_sort | trait selection strategy in multi-trait gwas: boosting snps discoverability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634875/ https://www.ncbi.nlm.nih.gov/pubmed/37961722 http://dx.doi.org/10.1101/2023.10.27.564319 |
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