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Identification of metabolic network models from incomplete high-throughput datasets
Motivation: High-throughput measurement techniques for metabolism and gene expression provide a wealth of information for the identification of metabolic network models. Yet, missing observations scattered over the dataset restrict the number of effectively available datapoints and make classical re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117355/ https://www.ncbi.nlm.nih.gov/pubmed/21685069 http://dx.doi.org/10.1093/bioinformatics/btr225 |
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author | Berthoumieux, Sara Brilli, Matteo de Jong, Hidde Kahn, Daniel Cinquemani, Eugenio |
author_facet | Berthoumieux, Sara Brilli, Matteo de Jong, Hidde Kahn, Daniel Cinquemani, Eugenio |
author_sort | Berthoumieux, Sara |
collection | PubMed |
description | Motivation: High-throughput measurement techniques for metabolism and gene expression provide a wealth of information for the identification of metabolic network models. Yet, missing observations scattered over the dataset restrict the number of effectively available datapoints and make classical regression techniques inaccurate or inapplicable. Thorough exploitation of the data by identification techniques that explicitly cope with missing observations is therefore of major importance. Results: We develop a maximum-likelihood approach for the estimation of unknown parameters of metabolic network models that relies on the integration of statistical priors to compensate for the missing data. In the context of the linlog metabolic modeling framework, we implement the identification method by an Expectation-Maximization (EM) algorithm and by a simpler direct numerical optimization method. We evaluate performance of our methods by comparison to existing approaches, and show that our EM method provides the best results over a variety of simulated scenarios. We then apply the EM algorithm to a real problem, the identification of a model for the Escherichia coli central carbon metabolism, based on challenging experimental data from the literature. This leads to promising results and allows us to highlight critical identification issues. Contact: sara.berthoumieux@inria.fr; eugenio.cinquemani@inria.fr Supplementary information: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-3117355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31173552011-06-17 Identification of metabolic network models from incomplete high-throughput datasets Berthoumieux, Sara Brilli, Matteo de Jong, Hidde Kahn, Daniel Cinquemani, Eugenio Bioinformatics Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria Motivation: High-throughput measurement techniques for metabolism and gene expression provide a wealth of information for the identification of metabolic network models. Yet, missing observations scattered over the dataset restrict the number of effectively available datapoints and make classical regression techniques inaccurate or inapplicable. Thorough exploitation of the data by identification techniques that explicitly cope with missing observations is therefore of major importance. Results: We develop a maximum-likelihood approach for the estimation of unknown parameters of metabolic network models that relies on the integration of statistical priors to compensate for the missing data. In the context of the linlog metabolic modeling framework, we implement the identification method by an Expectation-Maximization (EM) algorithm and by a simpler direct numerical optimization method. We evaluate performance of our methods by comparison to existing approaches, and show that our EM method provides the best results over a variety of simulated scenarios. We then apply the EM algorithm to a real problem, the identification of a model for the Escherichia coli central carbon metabolism, based on challenging experimental data from the literature. This leads to promising results and allows us to highlight critical identification issues. Contact: sara.berthoumieux@inria.fr; eugenio.cinquemani@inria.fr Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2011-07-01 2011-06-14 /pmc/articles/PMC3117355/ /pubmed/21685069 http://dx.doi.org/10.1093/bioinformatics/btr225 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria Berthoumieux, Sara Brilli, Matteo de Jong, Hidde Kahn, Daniel Cinquemani, Eugenio Identification of metabolic network models from incomplete high-throughput datasets |
title | Identification of metabolic network models from incomplete high-throughput datasets |
title_full | Identification of metabolic network models from incomplete high-throughput datasets |
title_fullStr | Identification of metabolic network models from incomplete high-throughput datasets |
title_full_unstemmed | Identification of metabolic network models from incomplete high-throughput datasets |
title_short | Identification of metabolic network models from incomplete high-throughput datasets |
title_sort | identification of metabolic network models from incomplete high-throughput datasets |
topic | Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117355/ https://www.ncbi.nlm.nih.gov/pubmed/21685069 http://dx.doi.org/10.1093/bioinformatics/btr225 |
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