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A framework for scalable parameter estimation of gene circuit models using structural information
Motivation: Systematic and scalable parameter estimation is a key to construct complex gene regulatory models and to ultimately facilitate an integrative systems biology approach to quantitatively understand the molecular mechanisms underpinning gene regulation. Results: Here, we report a novel fram...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694671/ https://www.ncbi.nlm.nih.gov/pubmed/23813015 http://dx.doi.org/10.1093/bioinformatics/btt232 |
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author | Kuwahara, Hiroyuki Fan, Ming Wang, Suojin Gao, Xin |
author_facet | Kuwahara, Hiroyuki Fan, Ming Wang, Suojin Gao, Xin |
author_sort | Kuwahara, Hiroyuki |
collection | PubMed |
description | Motivation: Systematic and scalable parameter estimation is a key to construct complex gene regulatory models and to ultimately facilitate an integrative systems biology approach to quantitatively understand the molecular mechanisms underpinning gene regulation. Results: Here, we report a novel framework for efficient and scalable parameter estimation that focuses specifically on modeling of gene circuits. Exploiting the structure commonly found in gene circuit models, this framework decomposes a system of coupled rate equations into individual ones and efficiently integrates them separately to reconstruct the mean time evolution of the gene products. The accuracy of the parameter estimates is refined by iteratively increasing the accuracy of numerical integration using the model structure. As a case study, we applied our framework to four gene circuit models with complex dynamics based on three synthetic datasets and one time series microarray data set. We compared our framework to three state-of-the-art parameter estimation methods and found that our approach consistently generated higher quality parameter solutions efficiently. Although many general-purpose parameter estimation methods have been applied for modeling of gene circuits, our results suggest that the use of more tailored approaches to use domain-specific information may be a key to reverse engineering of complex biological systems. Availability: http://sfb.kaust.edu.sa/Pages/Software.aspx Contact: xin.gao@kaust.edu.sa Supplementary information: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-3694671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36946712013-06-27 A framework for scalable parameter estimation of gene circuit models using structural information Kuwahara, Hiroyuki Fan, Ming Wang, Suojin Gao, Xin Bioinformatics Ismb/Eccb 2013 Proceedings Papers Committee July 21 to July 23, 2013, Berlin, Germany Motivation: Systematic and scalable parameter estimation is a key to construct complex gene regulatory models and to ultimately facilitate an integrative systems biology approach to quantitatively understand the molecular mechanisms underpinning gene regulation. Results: Here, we report a novel framework for efficient and scalable parameter estimation that focuses specifically on modeling of gene circuits. Exploiting the structure commonly found in gene circuit models, this framework decomposes a system of coupled rate equations into individual ones and efficiently integrates them separately to reconstruct the mean time evolution of the gene products. The accuracy of the parameter estimates is refined by iteratively increasing the accuracy of numerical integration using the model structure. As a case study, we applied our framework to four gene circuit models with complex dynamics based on three synthetic datasets and one time series microarray data set. We compared our framework to three state-of-the-art parameter estimation methods and found that our approach consistently generated higher quality parameter solutions efficiently. Although many general-purpose parameter estimation methods have been applied for modeling of gene circuits, our results suggest that the use of more tailored approaches to use domain-specific information may be a key to reverse engineering of complex biological systems. Availability: http://sfb.kaust.edu.sa/Pages/Software.aspx Contact: xin.gao@kaust.edu.sa Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2013-07-01 2013-06-19 /pmc/articles/PMC3694671/ /pubmed/23813015 http://dx.doi.org/10.1093/bioinformatics/btt232 Text en © The Author 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Ismb/Eccb 2013 Proceedings Papers Committee July 21 to July 23, 2013, Berlin, Germany Kuwahara, Hiroyuki Fan, Ming Wang, Suojin Gao, Xin A framework for scalable parameter estimation of gene circuit models using structural information |
title | A framework for scalable parameter estimation of gene circuit models using structural information |
title_full | A framework for scalable parameter estimation of gene circuit models using structural information |
title_fullStr | A framework for scalable parameter estimation of gene circuit models using structural information |
title_full_unstemmed | A framework for scalable parameter estimation of gene circuit models using structural information |
title_short | A framework for scalable parameter estimation of gene circuit models using structural information |
title_sort | framework for scalable parameter estimation of gene circuit models using structural information |
topic | Ismb/Eccb 2013 Proceedings Papers Committee July 21 to July 23, 2013, Berlin, Germany |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694671/ https://www.ncbi.nlm.nih.gov/pubmed/23813015 http://dx.doi.org/10.1093/bioinformatics/btt232 |
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