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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3464930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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