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A statistical approach to finding overlooked genetic associations
BACKGROUND: Complexity and noise in expression quantitative trait loci (eQTL) studies make it difficult to distinguish potential regulatory relationships among the many interactions. The predominant method of identifying eQTLs finds associations that are significant at a genome-wide level. The vast...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974753/ https://www.ncbi.nlm.nih.gov/pubmed/20964847 http://dx.doi.org/10.1186/1471-2105-11-526 |
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author | Rider, Andrew K Siwo, Geoffrey Chawla, Nitesh V Ferdig, Michael Emrich, Scott J |
author_facet | Rider, Andrew K Siwo, Geoffrey Chawla, Nitesh V Ferdig, Michael Emrich, Scott J |
author_sort | Rider, Andrew K |
collection | PubMed |
description | BACKGROUND: Complexity and noise in expression quantitative trait loci (eQTL) studies make it difficult to distinguish potential regulatory relationships among the many interactions. The predominant method of identifying eQTLs finds associations that are significant at a genome-wide level. The vast number of statistical tests carried out on these data make false negatives very likely. Corrections for multiple testing error render genome-wide eQTL techniques unable to detect modest regulatory effects. We propose an alternative method to identify eQTLs that builds on traditional approaches. In contrast to genome-wide techniques, our method determines the significance of an association between an expression trait and a locus with respect to the set of all associations to the expression trait. The use of this specific information facilitates identification of expression traits that have an expression profile that is characterized by a single exceptional association to a locus. Our approach identifies expression traits that have exceptional associations regardless of the genome-wide significance of those associations. This property facilitates the identification of possible false negatives for genome-wide significance. Further, our approach has the property of prioritizing expression traits that are affected by few strong associations. Expression traits identified by this method may warrant additional study because their expression level may be affected by targeting genes near a single locus. RESULTS: We demonstrate our method by identifying eQTL hotspots in Plasmodium falciparum (malaria) and Saccharomyces cerevisiae (yeast). We demonstrate the prioritization of traits with few strong genetic effects through Gene Ontology (GO) analysis of Yeast. Our results are strongly consistent with results gathered using genome-wide methods and identify additional hotspots and eQTLs. CONCLUSIONS: New eQTLs and hotspots found with this method may represent regions of the genome or biological processes that are controlled through few relatively strong genetic interactions. These points of interest warrant experimental investigation. |
format | Text |
id | pubmed-2974753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29747532010-11-08 A statistical approach to finding overlooked genetic associations Rider, Andrew K Siwo, Geoffrey Chawla, Nitesh V Ferdig, Michael Emrich, Scott J BMC Bioinformatics Methodology Article BACKGROUND: Complexity and noise in expression quantitative trait loci (eQTL) studies make it difficult to distinguish potential regulatory relationships among the many interactions. The predominant method of identifying eQTLs finds associations that are significant at a genome-wide level. The vast number of statistical tests carried out on these data make false negatives very likely. Corrections for multiple testing error render genome-wide eQTL techniques unable to detect modest regulatory effects. We propose an alternative method to identify eQTLs that builds on traditional approaches. In contrast to genome-wide techniques, our method determines the significance of an association between an expression trait and a locus with respect to the set of all associations to the expression trait. The use of this specific information facilitates identification of expression traits that have an expression profile that is characterized by a single exceptional association to a locus. Our approach identifies expression traits that have exceptional associations regardless of the genome-wide significance of those associations. This property facilitates the identification of possible false negatives for genome-wide significance. Further, our approach has the property of prioritizing expression traits that are affected by few strong associations. Expression traits identified by this method may warrant additional study because their expression level may be affected by targeting genes near a single locus. RESULTS: We demonstrate our method by identifying eQTL hotspots in Plasmodium falciparum (malaria) and Saccharomyces cerevisiae (yeast). We demonstrate the prioritization of traits with few strong genetic effects through Gene Ontology (GO) analysis of Yeast. Our results are strongly consistent with results gathered using genome-wide methods and identify additional hotspots and eQTLs. CONCLUSIONS: New eQTLs and hotspots found with this method may represent regions of the genome or biological processes that are controlled through few relatively strong genetic interactions. These points of interest warrant experimental investigation. BioMed Central 2010-10-21 /pmc/articles/PMC2974753/ /pubmed/20964847 http://dx.doi.org/10.1186/1471-2105-11-526 Text en Copyright ©2010 Rider 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 | Methodology Article Rider, Andrew K Siwo, Geoffrey Chawla, Nitesh V Ferdig, Michael Emrich, Scott J A statistical approach to finding overlooked genetic associations |
title | A statistical approach to finding overlooked genetic associations |
title_full | A statistical approach to finding overlooked genetic associations |
title_fullStr | A statistical approach to finding overlooked genetic associations |
title_full_unstemmed | A statistical approach to finding overlooked genetic associations |
title_short | A statistical approach to finding overlooked genetic associations |
title_sort | statistical approach to finding overlooked genetic associations |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974753/ https://www.ncbi.nlm.nih.gov/pubmed/20964847 http://dx.doi.org/10.1186/1471-2105-11-526 |
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