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DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data

BACKGROUND: Modeling dynamic regulatory networks is a major challenge since much of the protein-DNA interaction data available is static. The Dynamic Regulatory Events Miner (DREM) uses a Hidden Markov Model-based approach to integrate this static interaction data with time series gene expression le...

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Autores principales: Schulz, Marcel H, Devanny, William E, Gitter, Anthony, Zhong, Shan, Ernst, Jason, Bar-Joseph, Ziv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464930/
https://www.ncbi.nlm.nih.gov/pubmed/22897824
http://dx.doi.org/10.1186/1752-0509-6-104
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author Schulz, Marcel H
Devanny, William E
Gitter, Anthony
Zhong, Shan
Ernst, Jason
Bar-Joseph, Ziv
author_facet Schulz, Marcel H
Devanny, William E
Gitter, Anthony
Zhong, Shan
Ernst, Jason
Bar-Joseph, Ziv
author_sort Schulz, Marcel H
collection PubMed
description BACKGROUND: Modeling dynamic regulatory networks is a major challenge since much of the protein-DNA interaction data available is static. The Dynamic Regulatory Events Miner (DREM) uses a Hidden Markov Model-based approach to integrate this static interaction data with time series gene expression leading to models that can determine when transcription factors (TFs) activate genes and what genes they regulate. DREM has been used successfully in diverse areas of biological research. However, several issues were not addressed by the original version. RESULTS: DREM 2.0 is a comprehensive software for reconstructing dynamic regulatory networks that supports interactive graphical or batch mode. With version 2.0 a set of new features that are unique in comparison with other softwares are introduced. First, we provide static interaction data for additional species. Second, DREM 2.0 now accepts continuous binding values and we added a new method to utilize TF expression levels when searching for dynamic models. Third, we added support for discriminative motif discovery, which is particularly powerful for species with limited experimental interaction data. Finally, we improved the visualization to support the new features. Combined, these changes improve the ability of DREM 2.0 to accurately recover dynamic regulatory networks and make it much easier to use it for analyzing such networks in several species with varying degrees of interaction information. CONCLUSIONS: DREM 2.0 provides a unique framework for constructing and visualizing dynamic regulatory networks. DREM 2.0 can be downloaded from: www.sb.cs.cmu.edu/drem.
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spelling pubmed-34649302012-10-10 DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data Schulz, Marcel H Devanny, William E Gitter, Anthony Zhong, Shan Ernst, Jason Bar-Joseph, Ziv BMC Syst Biol Software BACKGROUND: Modeling dynamic regulatory networks is a major challenge since much of the protein-DNA interaction data available is static. The Dynamic Regulatory Events Miner (DREM) uses a Hidden Markov Model-based approach to integrate this static interaction data with time series gene expression leading to models that can determine when transcription factors (TFs) activate genes and what genes they regulate. DREM has been used successfully in diverse areas of biological research. However, several issues were not addressed by the original version. RESULTS: DREM 2.0 is a comprehensive software for reconstructing dynamic regulatory networks that supports interactive graphical or batch mode. With version 2.0 a set of new features that are unique in comparison with other softwares are introduced. First, we provide static interaction data for additional species. Second, DREM 2.0 now accepts continuous binding values and we added a new method to utilize TF expression levels when searching for dynamic models. Third, we added support for discriminative motif discovery, which is particularly powerful for species with limited experimental interaction data. Finally, we improved the visualization to support the new features. Combined, these changes improve the ability of DREM 2.0 to accurately recover dynamic regulatory networks and make it much easier to use it for analyzing such networks in several species with varying degrees of interaction information. CONCLUSIONS: DREM 2.0 provides a unique framework for constructing and visualizing dynamic regulatory networks. DREM 2.0 can be downloaded from: www.sb.cs.cmu.edu/drem. BioMed Central 2012-08-16 /pmc/articles/PMC3464930/ /pubmed/22897824 http://dx.doi.org/10.1186/1752-0509-6-104 Text en Copyright ©2012 Schulz 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 Software
Schulz, Marcel H
Devanny, William E
Gitter, Anthony
Zhong, Shan
Ernst, Jason
Bar-Joseph, Ziv
DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
title DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
title_full DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
title_fullStr DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
title_full_unstemmed DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
title_short DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
title_sort drem 2.0: improved reconstruction of dynamic regulatory networks from time-series expression data
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464930/
https://www.ncbi.nlm.nih.gov/pubmed/22897824
http://dx.doi.org/10.1186/1752-0509-6-104
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