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Sparse regression models for unraveling group and individual associations in eQTL mapping
BACKGROUND: As a promising tool for dissecting the genetic basis of common diseases, expression quantitative trait loci (eQTL) study has attracted increasing research interest. Traditional eQTL methods focus on testing the associations between individual single-nucleotide polymorphisms (SNPs) and ge...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802846/ https://www.ncbi.nlm.nih.gov/pubmed/27000043 http://dx.doi.org/10.1186/s12859-016-0986-9 |
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author | Cheng, Wei Shi, Yu Zhang, Xiang Wang, Wei |
author_facet | Cheng, Wei Shi, Yu Zhang, Xiang Wang, Wei |
author_sort | Cheng, Wei |
collection | PubMed |
description | BACKGROUND: As a promising tool for dissecting the genetic basis of common diseases, expression quantitative trait loci (eQTL) study has attracted increasing research interest. Traditional eQTL methods focus on testing the associations between individual single-nucleotide polymorphisms (SNPs) and gene expression traits. A major drawback of this approach is that it cannot model the joint effect of a set of SNPs on a set of genes, which may correspond to biological pathways. RESULTS: To alleviate this limitation, in this paper, we propose geQTL, a sparse regression method that can detect both group-wise and individual associations between SNPs and expression traits. geQTL can also correct the effects of potential confounders. Our method employs computationally efficient technique, thus it is able to fulfill large scale studies. Moreover, our method can automatically infer the proper number of group-wise associations. We perform extensive experiments on both simulated datasets and yeast datasets to demonstrate the effectiveness and efficiency of the proposed method. The results show that geQTL can effectively detect both individual and group-wise signals and outperforms the state-of-the-arts by a large margin. CONCLUSIONS: This paper well illustrates that decoupling individual and group-wise associations for association mapping is able to improve eQTL mapping accuracy, and inferring individual and group-wise associations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-0986-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4802846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48028462016-03-23 Sparse regression models for unraveling group and individual associations in eQTL mapping Cheng, Wei Shi, Yu Zhang, Xiang Wang, Wei BMC Bioinformatics Research Article BACKGROUND: As a promising tool for dissecting the genetic basis of common diseases, expression quantitative trait loci (eQTL) study has attracted increasing research interest. Traditional eQTL methods focus on testing the associations between individual single-nucleotide polymorphisms (SNPs) and gene expression traits. A major drawback of this approach is that it cannot model the joint effect of a set of SNPs on a set of genes, which may correspond to biological pathways. RESULTS: To alleviate this limitation, in this paper, we propose geQTL, a sparse regression method that can detect both group-wise and individual associations between SNPs and expression traits. geQTL can also correct the effects of potential confounders. Our method employs computationally efficient technique, thus it is able to fulfill large scale studies. Moreover, our method can automatically infer the proper number of group-wise associations. We perform extensive experiments on both simulated datasets and yeast datasets to demonstrate the effectiveness and efficiency of the proposed method. The results show that geQTL can effectively detect both individual and group-wise signals and outperforms the state-of-the-arts by a large margin. CONCLUSIONS: This paper well illustrates that decoupling individual and group-wise associations for association mapping is able to improve eQTL mapping accuracy, and inferring individual and group-wise associations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-0986-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-22 /pmc/articles/PMC4802846/ /pubmed/27000043 http://dx.doi.org/10.1186/s12859-016-0986-9 Text en © Cheng et al. 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Cheng, Wei Shi, Yu Zhang, Xiang Wang, Wei Sparse regression models for unraveling group and individual associations in eQTL mapping |
title | Sparse regression models for unraveling group and individual associations in eQTL mapping |
title_full | Sparse regression models for unraveling group and individual associations in eQTL mapping |
title_fullStr | Sparse regression models for unraveling group and individual associations in eQTL mapping |
title_full_unstemmed | Sparse regression models for unraveling group and individual associations in eQTL mapping |
title_short | Sparse regression models for unraveling group and individual associations in eQTL mapping |
title_sort | sparse regression models for unraveling group and individual associations in eqtl mapping |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802846/ https://www.ncbi.nlm.nih.gov/pubmed/27000043 http://dx.doi.org/10.1186/s12859-016-0986-9 |
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