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Grouped graphical Granger modeling for gene expression regulatory networks discovery

We consider the problem of discovering gene regulatory networks from time-series microarray data. Recently, graphical Granger modeling has gained considerable attention as a promising direction for addressing this problem. These methods apply graphical modeling methods on time-series data and invoke...

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Autores principales: Lozano, Aurélie C., Abe, Naoki, Liu, Yan, Rosset, Saharon
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687953/
https://www.ncbi.nlm.nih.gov/pubmed/19477976
http://dx.doi.org/10.1093/bioinformatics/btp199
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author Lozano, Aurélie C.
Abe, Naoki
Liu, Yan
Rosset, Saharon
author_facet Lozano, Aurélie C.
Abe, Naoki
Liu, Yan
Rosset, Saharon
author_sort Lozano, Aurélie C.
collection PubMed
description We consider the problem of discovering gene regulatory networks from time-series microarray data. Recently, graphical Granger modeling has gained considerable attention as a promising direction for addressing this problem. These methods apply graphical modeling methods on time-series data and invoke the notion of ‘Granger causality’ to make assertions on causality through inference on time-lagged effects. Existing algorithms, however, have neglected an important aspect of the problem—the group structure among the lagged temporal variables naturally imposed by the time series they belong to. Specifically, existing methods in computational biology share this shortcoming, as well as additional computational limitations, prohibiting their effective applications to the large datasets including a large number of genes and many data points. In the present article, we propose a novel methodology which we term ‘grouped graphical Granger modeling method’, which overcomes the limitations mentioned above by applying a regression method suited for high-dimensional and large data, and by leveraging the group structure among the lagged temporal variables according to the time series they belong to. We demonstrate the effectiveness of the proposed methodology on both simulated and actual gene expression data, specifically the human cancer cell (HeLa S3) cycle data. The simulation results show that the proposed methodology generally exhibits higher accuracy in recovering the underlying causal structure. Those on the gene expression data demonstrate that it leads to improved accuracy with respect to prediction of known links, and also uncovers additional causal relationships uncaptured by earlier works. Contact: aclozano@us.ibm.com
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spelling pubmed-26879532009-06-02 Grouped graphical Granger modeling for gene expression regulatory networks discovery Lozano, Aurélie C. Abe, Naoki Liu, Yan Rosset, Saharon Bioinformatics Ismb/Eccb 2009 Conference Proceedings June 27 to July 2, 2009, Stockholm, Sweden We consider the problem of discovering gene regulatory networks from time-series microarray data. Recently, graphical Granger modeling has gained considerable attention as a promising direction for addressing this problem. These methods apply graphical modeling methods on time-series data and invoke the notion of ‘Granger causality’ to make assertions on causality through inference on time-lagged effects. Existing algorithms, however, have neglected an important aspect of the problem—the group structure among the lagged temporal variables naturally imposed by the time series they belong to. Specifically, existing methods in computational biology share this shortcoming, as well as additional computational limitations, prohibiting their effective applications to the large datasets including a large number of genes and many data points. In the present article, we propose a novel methodology which we term ‘grouped graphical Granger modeling method’, which overcomes the limitations mentioned above by applying a regression method suited for high-dimensional and large data, and by leveraging the group structure among the lagged temporal variables according to the time series they belong to. We demonstrate the effectiveness of the proposed methodology on both simulated and actual gene expression data, specifically the human cancer cell (HeLa S3) cycle data. The simulation results show that the proposed methodology generally exhibits higher accuracy in recovering the underlying causal structure. Those on the gene expression data demonstrate that it leads to improved accuracy with respect to prediction of known links, and also uncovers additional causal relationships uncaptured by earlier works. Contact: aclozano@us.ibm.com Oxford University Press 2009-06-15 2009-05-27 /pmc/articles/PMC2687953/ /pubmed/19477976 http://dx.doi.org/10.1093/bioinformatics/btp199 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Ismb/Eccb 2009 Conference Proceedings June 27 to July 2, 2009, Stockholm, Sweden
Lozano, Aurélie C.
Abe, Naoki
Liu, Yan
Rosset, Saharon
Grouped graphical Granger modeling for gene expression regulatory networks discovery
title Grouped graphical Granger modeling for gene expression regulatory networks discovery
title_full Grouped graphical Granger modeling for gene expression regulatory networks discovery
title_fullStr Grouped graphical Granger modeling for gene expression regulatory networks discovery
title_full_unstemmed Grouped graphical Granger modeling for gene expression regulatory networks discovery
title_short Grouped graphical Granger modeling for gene expression regulatory networks discovery
title_sort grouped graphical granger modeling for gene expression regulatory networks discovery
topic Ismb/Eccb 2009 Conference Proceedings June 27 to July 2, 2009, Stockholm, Sweden
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687953/
https://www.ncbi.nlm.nih.gov/pubmed/19477976
http://dx.doi.org/10.1093/bioinformatics/btp199
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