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Graph-regularized dual Lasso for robust eQTL mapping

Motivation: As a promising tool for dissecting the genetic basis of complex traits, expression quantitative trait loci (eQTL) mapping has attracted increasing research interest. An important issue in eQTL mapping is how to effectively integrate networks representing interactions among genetic marker...

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Autores principales: Cheng, Wei, Zhang, Xiang, Guo, Zhishan, Shi, Yu, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058913/
https://www.ncbi.nlm.nih.gov/pubmed/24931977
http://dx.doi.org/10.1093/bioinformatics/btu293
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author Cheng, Wei
Zhang, Xiang
Guo, Zhishan
Shi, Yu
Wang, Wei
author_facet Cheng, Wei
Zhang, Xiang
Guo, Zhishan
Shi, Yu
Wang, Wei
author_sort Cheng, Wei
collection PubMed
description Motivation: As a promising tool for dissecting the genetic basis of complex traits, expression quantitative trait loci (eQTL) mapping has attracted increasing research interest. An important issue in eQTL mapping is how to effectively integrate networks representing interactions among genetic markers and genes. Recently, several Lasso-based methods have been proposed to leverage such network information. Despite their success, existing methods have three common limitations: (i) a preprocessing step is usually needed to cluster the networks; (ii) the incompleteness of the networks and the noise in them are not considered; (iii) other available information, such as location of genetic markers and pathway information are not integrated. Results: To address the limitations of the existing methods, we propose Graph-regularized Dual Lasso (GDL), a robust approach for eQTL mapping. GDL integrates the correlation structures among genetic markers and traits simultaneously. It also takes into account the incompleteness of the networks and is robust to the noise. GDL utilizes graph-based regularizers to model the prior networks and does not require an explicit clustering step. Moreover, it enables further refinement of the partial and noisy networks. We further generalize GDL to incorporate the location of genetic makers and gene-pathway information. We perform extensive experimental evaluations using both simulated and real datasets. Experimental results demonstrate that the proposed methods can effectively integrate various available priori knowledge and significantly outperform the state-of-the-art eQTL mapping methods. Availability: Software for both C++ version and Matlab version is available at http://www.cs.unc.edu/∼weicheng/. Contact: weiwang@cs.ucla.edu Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-40589132014-06-18 Graph-regularized dual Lasso for robust eQTL mapping Cheng, Wei Zhang, Xiang Guo, Zhishan Shi, Yu Wang, Wei Bioinformatics Ismb 2014 Proceedings Papers Committee Motivation: As a promising tool for dissecting the genetic basis of complex traits, expression quantitative trait loci (eQTL) mapping has attracted increasing research interest. An important issue in eQTL mapping is how to effectively integrate networks representing interactions among genetic markers and genes. Recently, several Lasso-based methods have been proposed to leverage such network information. Despite their success, existing methods have three common limitations: (i) a preprocessing step is usually needed to cluster the networks; (ii) the incompleteness of the networks and the noise in them are not considered; (iii) other available information, such as location of genetic markers and pathway information are not integrated. Results: To address the limitations of the existing methods, we propose Graph-regularized Dual Lasso (GDL), a robust approach for eQTL mapping. GDL integrates the correlation structures among genetic markers and traits simultaneously. It also takes into account the incompleteness of the networks and is robust to the noise. GDL utilizes graph-based regularizers to model the prior networks and does not require an explicit clustering step. Moreover, it enables further refinement of the partial and noisy networks. We further generalize GDL to incorporate the location of genetic makers and gene-pathway information. We perform extensive experimental evaluations using both simulated and real datasets. Experimental results demonstrate that the proposed methods can effectively integrate various available priori knowledge and significantly outperform the state-of-the-art eQTL mapping methods. Availability: Software for both C++ version and Matlab version is available at http://www.cs.unc.edu/∼weicheng/. Contact: weiwang@cs.ucla.edu Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2014-06-15 2014-06-11 /pmc/articles/PMC4058913/ /pubmed/24931977 http://dx.doi.org/10.1093/bioinformatics/btu293 Text en © The Author 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Ismb 2014 Proceedings Papers Committee
Cheng, Wei
Zhang, Xiang
Guo, Zhishan
Shi, Yu
Wang, Wei
Graph-regularized dual Lasso for robust eQTL mapping
title Graph-regularized dual Lasso for robust eQTL mapping
title_full Graph-regularized dual Lasso for robust eQTL mapping
title_fullStr Graph-regularized dual Lasso for robust eQTL mapping
title_full_unstemmed Graph-regularized dual Lasso for robust eQTL mapping
title_short Graph-regularized dual Lasso for robust eQTL mapping
title_sort graph-regularized dual lasso for robust eqtl mapping
topic Ismb 2014 Proceedings Papers Committee
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058913/
https://www.ncbi.nlm.nih.gov/pubmed/24931977
http://dx.doi.org/10.1093/bioinformatics/btu293
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