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Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies
BACKGROUND: A rapidly growing amount of knowledge about signaling and gene regulatory networks is available in databases such as KEGG, Reactome, or RegulonDB. There is an increasing need to relate this knowledge to high-throughput data in order to (in)validate network topologies or to decide which i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625540/ https://www.ncbi.nlm.nih.gov/pubmed/26510976 http://dx.doi.org/10.1186/s12859-015-0733-7 |
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author | Thiele, Sven Cerone, Luca Saez-Rodriguez, Julio Siegel, Anne Guziołowski, Carito Klamt, Steffen |
author_facet | Thiele, Sven Cerone, Luca Saez-Rodriguez, Julio Siegel, Anne Guziołowski, Carito Klamt, Steffen |
author_sort | Thiele, Sven |
collection | PubMed |
description | BACKGROUND: A rapidly growing amount of knowledge about signaling and gene regulatory networks is available in databases such as KEGG, Reactome, or RegulonDB. There is an increasing need to relate this knowledge to high-throughput data in order to (in)validate network topologies or to decide which interactions are present or inactive in a given cell type under a particular environmental condition. Interaction graphs provide a suitable representation of cellular networks with information flows and methods based on sign consistency approaches have been shown to be valuable tools to (i) predict qualitative responses, (ii) to test the consistency of network topologies and experimental data, and (iii) to apply repair operations to the network model suggesting missing or wrong interactions. RESULTS: We present a framework to unify different notions of sign consistency and propose a refined method for data discretization that considers uncertainties in experimental profiles. We furthermore introduce a new constraint to filter undesired model behaviors induced by positive feedback loops. Finally, we generalize the way predictions can be made by the sign consistency approach. In particular, we distinguish strong predictions (e.g. increase of a node level) and weak predictions (e.g., node level increases or remains unchanged) enlarging the overall predictive power of the approach. We then demonstrate the applicability of our framework by confronting a large-scale gene regulatory network model of Escherichia coli with high-throughput transcriptomic measurements. CONCLUSION: Overall, our work enhances the flexibility and power of the sign consistency approach for the prediction of the behavior of signaling and gene regulatory networks and, more generally, for the validation and inference of these networks ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0733-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4625540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46255402015-10-30 Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies Thiele, Sven Cerone, Luca Saez-Rodriguez, Julio Siegel, Anne Guziołowski, Carito Klamt, Steffen BMC Bioinformatics Methodology Article BACKGROUND: A rapidly growing amount of knowledge about signaling and gene regulatory networks is available in databases such as KEGG, Reactome, or RegulonDB. There is an increasing need to relate this knowledge to high-throughput data in order to (in)validate network topologies or to decide which interactions are present or inactive in a given cell type under a particular environmental condition. Interaction graphs provide a suitable representation of cellular networks with information flows and methods based on sign consistency approaches have been shown to be valuable tools to (i) predict qualitative responses, (ii) to test the consistency of network topologies and experimental data, and (iii) to apply repair operations to the network model suggesting missing or wrong interactions. RESULTS: We present a framework to unify different notions of sign consistency and propose a refined method for data discretization that considers uncertainties in experimental profiles. We furthermore introduce a new constraint to filter undesired model behaviors induced by positive feedback loops. Finally, we generalize the way predictions can be made by the sign consistency approach. In particular, we distinguish strong predictions (e.g. increase of a node level) and weak predictions (e.g., node level increases or remains unchanged) enlarging the overall predictive power of the approach. We then demonstrate the applicability of our framework by confronting a large-scale gene regulatory network model of Escherichia coli with high-throughput transcriptomic measurements. CONCLUSION: Overall, our work enhances the flexibility and power of the sign consistency approach for the prediction of the behavior of signaling and gene regulatory networks and, more generally, for the validation and inference of these networks ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0733-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-28 /pmc/articles/PMC4625540/ /pubmed/26510976 http://dx.doi.org/10.1186/s12859-015-0733-7 Text en © Thiele et al. 2015 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 | Methodology Article Thiele, Sven Cerone, Luca Saez-Rodriguez, Julio Siegel, Anne Guziołowski, Carito Klamt, Steffen Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
title | Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
title_full | Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
title_fullStr | Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
title_full_unstemmed | Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
title_short | Extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
title_sort | extended notions of sign consistency to relate experimental data to signaling and regulatory network topologies |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625540/ https://www.ncbi.nlm.nih.gov/pubmed/26510976 http://dx.doi.org/10.1186/s12859-015-0733-7 |
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