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On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies
BACKGROUND: Genome-wide association studies (GWAS) with metabolic traits and metabolome-wide association studies (MWAS) with traits of biomedical relevance are powerful tools to identify the contribution of genetic, environmental and lifestyle factors to the etiology of complex diseases. Hypothesis-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537592/ https://www.ncbi.nlm.nih.gov/pubmed/22672667 http://dx.doi.org/10.1186/1471-2105-13-120 |
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author | Petersen, Ann-Kristin Krumsiek, Jan Wägele, Brigitte Theis, Fabian J Wichmann, H-Erich Gieger, Christian Suhre, Karsten |
author_facet | Petersen, Ann-Kristin Krumsiek, Jan Wägele, Brigitte Theis, Fabian J Wichmann, H-Erich Gieger, Christian Suhre, Karsten |
author_sort | Petersen, Ann-Kristin |
collection | PubMed |
description | BACKGROUND: Genome-wide association studies (GWAS) with metabolic traits and metabolome-wide association studies (MWAS) with traits of biomedical relevance are powerful tools to identify the contribution of genetic, environmental and lifestyle factors to the etiology of complex diseases. Hypothesis-free testing of ratios between all possible metabolite pairs in GWAS and MWAS has proven to be an innovative approach in the discovery of new biologically meaningful associations. The p-gain statistic was introduced as an ad-hoc measure to determine whether a ratio between two metabolite concentrations carries more information than the two corresponding metabolite concentrations alone. So far, only a rule of thumb was applied to determine the significance of the p-gain. RESULTS: Here we explore the statistical properties of the p-gain through simulation of its density and by sampling of experimental data. We derive critical values of the p-gain for different levels of correlation between metabolite pairs and show that B/(2*α) is a conservative critical value for the p-gain, where α is the level of significance and B the number of tested metabolite pairs. CONCLUSIONS: We show that the p-gain is a well defined measure that can be used to identify statistically significant metabolite ratios in association studies and provide a conservative significance cut-off for the p-gain for use in future association studies with metabolic traits. |
format | Online Article Text |
id | pubmed-3537592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35375922013-01-10 On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies Petersen, Ann-Kristin Krumsiek, Jan Wägele, Brigitte Theis, Fabian J Wichmann, H-Erich Gieger, Christian Suhre, Karsten BMC Bioinformatics Research Article BACKGROUND: Genome-wide association studies (GWAS) with metabolic traits and metabolome-wide association studies (MWAS) with traits of biomedical relevance are powerful tools to identify the contribution of genetic, environmental and lifestyle factors to the etiology of complex diseases. Hypothesis-free testing of ratios between all possible metabolite pairs in GWAS and MWAS has proven to be an innovative approach in the discovery of new biologically meaningful associations. The p-gain statistic was introduced as an ad-hoc measure to determine whether a ratio between two metabolite concentrations carries more information than the two corresponding metabolite concentrations alone. So far, only a rule of thumb was applied to determine the significance of the p-gain. RESULTS: Here we explore the statistical properties of the p-gain through simulation of its density and by sampling of experimental data. We derive critical values of the p-gain for different levels of correlation between metabolite pairs and show that B/(2*α) is a conservative critical value for the p-gain, where α is the level of significance and B the number of tested metabolite pairs. CONCLUSIONS: We show that the p-gain is a well defined measure that can be used to identify statistically significant metabolite ratios in association studies and provide a conservative significance cut-off for the p-gain for use in future association studies with metabolic traits. BioMed Central 2012-06-06 /pmc/articles/PMC3537592/ /pubmed/22672667 http://dx.doi.org/10.1186/1471-2105-13-120 Text en Copyright ©2012 Petersen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Petersen, Ann-Kristin Krumsiek, Jan Wägele, Brigitte Theis, Fabian J Wichmann, H-Erich Gieger, Christian Suhre, Karsten On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
title | On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
title_full | On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
title_fullStr | On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
title_full_unstemmed | On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
title_short | On the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
title_sort | on the hypothesis-free testing of metabolite ratios in genome-wide and metabolome-wide association studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537592/ https://www.ncbi.nlm.nih.gov/pubmed/22672667 http://dx.doi.org/10.1186/1471-2105-13-120 |
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