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Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests
Testing for association between a set of genetic markers and a phenotype is a fundamental task in genetic studies. Standard approaches for heritability and set testing strongly rely on parametric models that make specific assumptions regarding phenotypic variability. Here, we show that resulting p-v...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249264/ https://www.ncbi.nlm.nih.gov/pubmed/30464216 http://dx.doi.org/10.1038/s41467-018-07276-w |
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author | Schweiger, Regev Fisher, Eyal Weissbrod, Omer Rahmani, Elior Müller-Nurasyid, Martina Kunze, Sonja Gieger, Christian Waldenberger, Melanie Rosset, Saharon Halperin, Eran |
author_facet | Schweiger, Regev Fisher, Eyal Weissbrod, Omer Rahmani, Elior Müller-Nurasyid, Martina Kunze, Sonja Gieger, Christian Waldenberger, Melanie Rosset, Saharon Halperin, Eran |
author_sort | Schweiger, Regev |
collection | PubMed |
description | Testing for association between a set of genetic markers and a phenotype is a fundamental task in genetic studies. Standard approaches for heritability and set testing strongly rely on parametric models that make specific assumptions regarding phenotypic variability. Here, we show that resulting p-values may be inflated by up to 15 orders of magnitude, in a heritability study of methylation measurements, and in a heritability and expression quantitative trait loci analysis of gene expression profiles. We propose FEATHER, a method for fast permutation-based testing of marker sets and of heritability, which properly controls for false-positive results. FEATHER eliminated 47% of methylation sites found to be heritable by the parametric test, suggesting a substantial inflation of false-positive findings by alternative methods. Our approach can rapidly identify heritable phenotypes out of millions of phenotypes acquired via high-throughput technologies, does not suffer from model misspecification and is highly efficient. |
format | Online Article Text |
id | pubmed-6249264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62492642018-11-26 Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests Schweiger, Regev Fisher, Eyal Weissbrod, Omer Rahmani, Elior Müller-Nurasyid, Martina Kunze, Sonja Gieger, Christian Waldenberger, Melanie Rosset, Saharon Halperin, Eran Nat Commun Article Testing for association between a set of genetic markers and a phenotype is a fundamental task in genetic studies. Standard approaches for heritability and set testing strongly rely on parametric models that make specific assumptions regarding phenotypic variability. Here, we show that resulting p-values may be inflated by up to 15 orders of magnitude, in a heritability study of methylation measurements, and in a heritability and expression quantitative trait loci analysis of gene expression profiles. We propose FEATHER, a method for fast permutation-based testing of marker sets and of heritability, which properly controls for false-positive results. FEATHER eliminated 47% of methylation sites found to be heritable by the parametric test, suggesting a substantial inflation of false-positive findings by alternative methods. Our approach can rapidly identify heritable phenotypes out of millions of phenotypes acquired via high-throughput technologies, does not suffer from model misspecification and is highly efficient. Nature Publishing Group UK 2018-11-21 /pmc/articles/PMC6249264/ /pubmed/30464216 http://dx.doi.org/10.1038/s41467-018-07276-w Text en © The Author(s) 2018 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/. |
spellingShingle | Article Schweiger, Regev Fisher, Eyal Weissbrod, Omer Rahmani, Elior Müller-Nurasyid, Martina Kunze, Sonja Gieger, Christian Waldenberger, Melanie Rosset, Saharon Halperin, Eran Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
title | Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
title_full | Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
title_fullStr | Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
title_full_unstemmed | Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
title_short | Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
title_sort | detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249264/ https://www.ncbi.nlm.nih.gov/pubmed/30464216 http://dx.doi.org/10.1038/s41467-018-07276-w |
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