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Data-driven reverse engineering of signaling pathways using ensembles of dynamic models
Despite significant efforts and remarkable progress, the inference of signaling networks from experimental data remains very challenging. The problem is particularly difficult when the objective is to obtain a dynamic model capable of predicting the effect of novel perturbations not considered durin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319798/ https://www.ncbi.nlm.nih.gov/pubmed/28166222 http://dx.doi.org/10.1371/journal.pcbi.1005379 |
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author | Henriques, David Villaverde, Alejandro F. Rocha, Miguel Saez-Rodriguez, Julio Banga, Julio R. |
author_facet | Henriques, David Villaverde, Alejandro F. Rocha, Miguel Saez-Rodriguez, Julio Banga, Julio R. |
author_sort | Henriques, David |
collection | PubMed |
description | Despite significant efforts and remarkable progress, the inference of signaling networks from experimental data remains very challenging. The problem is particularly difficult when the objective is to obtain a dynamic model capable of predicting the effect of novel perturbations not considered during model training. The problem is ill-posed due to the nonlinear nature of these systems, the fact that only a fraction of the involved proteins and their post-translational modifications can be measured, and limitations on the technologies used for growing cells in vitro, perturbing them, and measuring their variations. As a consequence, there is a pervasive lack of identifiability. To overcome these issues, we present a methodology called SELDOM (enSEmbLe of Dynamic lOgic-based Models), which builds an ensemble of logic-based dynamic models, trains them to experimental data, and combines their individual simulations into an ensemble prediction. It also includes a model reduction step to prune spurious interactions and mitigate overfitting. SELDOM is a data-driven method, in the sense that it does not require any prior knowledge of the system: the interaction networks that act as scaffolds for the dynamic models are inferred from data using mutual information. We have tested SELDOM on a number of experimental and in silico signal transduction case-studies, including the recent HPN-DREAM breast cancer challenge. We found that its performance is highly competitive compared to state-of-the-art methods for the purpose of recovering network topology. More importantly, the utility of SELDOM goes beyond basic network inference (i.e. uncovering static interaction networks): it builds dynamic (based on ordinary differential equation) models, which can be used for mechanistic interpretations and reliable dynamic predictions in new experimental conditions (i.e. not used in the training). For this task, SELDOM’s ensemble prediction is not only consistently better than predictions from individual models, but also often outperforms the state of the art represented by the methods used in the HPN-DREAM challenge. |
format | Online Article Text |
id | pubmed-5319798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53197982017-03-03 Data-driven reverse engineering of signaling pathways using ensembles of dynamic models Henriques, David Villaverde, Alejandro F. Rocha, Miguel Saez-Rodriguez, Julio Banga, Julio R. PLoS Comput Biol Research Article Despite significant efforts and remarkable progress, the inference of signaling networks from experimental data remains very challenging. The problem is particularly difficult when the objective is to obtain a dynamic model capable of predicting the effect of novel perturbations not considered during model training. The problem is ill-posed due to the nonlinear nature of these systems, the fact that only a fraction of the involved proteins and their post-translational modifications can be measured, and limitations on the technologies used for growing cells in vitro, perturbing them, and measuring their variations. As a consequence, there is a pervasive lack of identifiability. To overcome these issues, we present a methodology called SELDOM (enSEmbLe of Dynamic lOgic-based Models), which builds an ensemble of logic-based dynamic models, trains them to experimental data, and combines their individual simulations into an ensemble prediction. It also includes a model reduction step to prune spurious interactions and mitigate overfitting. SELDOM is a data-driven method, in the sense that it does not require any prior knowledge of the system: the interaction networks that act as scaffolds for the dynamic models are inferred from data using mutual information. We have tested SELDOM on a number of experimental and in silico signal transduction case-studies, including the recent HPN-DREAM breast cancer challenge. We found that its performance is highly competitive compared to state-of-the-art methods for the purpose of recovering network topology. More importantly, the utility of SELDOM goes beyond basic network inference (i.e. uncovering static interaction networks): it builds dynamic (based on ordinary differential equation) models, which can be used for mechanistic interpretations and reliable dynamic predictions in new experimental conditions (i.e. not used in the training). For this task, SELDOM’s ensemble prediction is not only consistently better than predictions from individual models, but also often outperforms the state of the art represented by the methods used in the HPN-DREAM challenge. Public Library of Science 2017-02-06 /pmc/articles/PMC5319798/ /pubmed/28166222 http://dx.doi.org/10.1371/journal.pcbi.1005379 Text en © 2017 Henriques et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Henriques, David Villaverde, Alejandro F. Rocha, Miguel Saez-Rodriguez, Julio Banga, Julio R. Data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
title | Data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
title_full | Data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
title_fullStr | Data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
title_full_unstemmed | Data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
title_short | Data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
title_sort | data-driven reverse engineering of signaling pathways using ensembles of dynamic models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319798/ https://www.ncbi.nlm.nih.gov/pubmed/28166222 http://dx.doi.org/10.1371/journal.pcbi.1005379 |
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