Data-driven reverse engineering of signaling pathways using ensembles of dynamic models

Detalhes bibliográficos
Autor(a) principal: Henriques, David
Data de Publicação: 2017
Outros Autores: Villaverde, Alejandro F., Rocha, Miguel, Saez-Rodriguez, Julio, Banga, Julio R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/47805
Resumo: Signaling pathways play a key role in complex diseases such as cancer, for which the development of novel therapies is a difficult, expensive and laborious task. Computational models that can predict the effect of a new combination of drugs without having to test it experimentally can help in accelerating this process. In particular, network-based dynamic models of these pathways hold promise to both understand and predict the effect of therapeutics. However, their use is currently hampered by limitations in our knowledge of the underlying biochemistry, as well as in the experimental and computational technologies used for calibrating the models. Thus, the results from such models need to be carefully interpreted and used in order to avoid biased predictions. Here we present a procedure that deals with this uncertainty by using experimental data to build an ensemble of dynamic models. The method incorporates steps to reduce overfitting and maximize predictive capability. We find that by combining the outputs of individual models in an ensemble it is possible to obtain a more robust prediction. We report results obtained with this method, which we call SELDOM (enSEmbLe of Dynamic lOgic-based Models), showing that it improves the predictions previously reported for several challenging problems.
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spelling Data-driven reverse engineering of signaling pathways using ensembles of dynamic modelsScience & TechnologySignaling pathways play a key role in complex diseases such as cancer, for which the development of novel therapies is a difficult, expensive and laborious task. Computational models that can predict the effect of a new combination of drugs without having to test it experimentally can help in accelerating this process. In particular, network-based dynamic models of these pathways hold promise to both understand and predict the effect of therapeutics. However, their use is currently hampered by limitations in our knowledge of the underlying biochemistry, as well as in the experimental and computational technologies used for calibrating the models. Thus, the results from such models need to be carefully interpreted and used in order to avoid biased predictions. Here we present a procedure that deals with this uncertainty by using experimental data to build an ensemble of dynamic models. The method incorporates steps to reduce overfitting and maximize predictive capability. We find that by combining the outputs of individual models in an ensemble it is possible to obtain a more robust prediction. We report results obtained with this method, which we call SELDOM (enSEmbLe of Dynamic lOgic-based Models), showing that it improves the predictions previously reported for several challenging problems.JRB and DH acknowledge funding from the EU FP7 project NICHE (ITN Grant number 289384). JRB acknowledges funding from the Spanish MINECO project SYNBIOFACTORY (grant number DPI2014-55276-C5-2-R). AFV acknowledges funding from the Galician government (Xunta de Galiza) through the I2C postdoctoral fellowship ED481B2014/133-0. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.info:eu-repo/semantics/publishedVersionPublic Library of Science (PLOS)Universidade do MinhoHenriques, DavidVillaverde, Alejandro F.Rocha, MiguelSaez-Rodriguez, JulioBanga, Julio R.2017-02-062017-02-06T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/47805engHenriques, David; Villaverde, Alejandro F.; Rocha, Miguel; Saez-Rodriguez, Julio; Banga, Julio R., Data-driven reverse engineering of signaling pathways using ensembles of dynamic models. PLoS Computational Biology, 13(2), 1-25, 20171553-734X1553-735810.1371/journal.pcbi.100537928166222http://journals.plos.org/ploscompbiol/info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:53:35Zoai:repositorium.sdum.uminho.pt:1822/47805Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:52:59.696610Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv 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
spellingShingle Data-driven reverse engineering of signaling pathways using ensembles of dynamic models
Henriques, David
Science & Technology
title_short 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_sort Data-driven reverse engineering of signaling pathways using ensembles of dynamic models
author Henriques, David
author_facet Henriques, David
Villaverde, Alejandro F.
Rocha, Miguel
Saez-Rodriguez, Julio
Banga, Julio R.
author_role author
author2 Villaverde, Alejandro F.
Rocha, Miguel
Saez-Rodriguez, Julio
Banga, Julio R.
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Henriques, David
Villaverde, Alejandro F.
Rocha, Miguel
Saez-Rodriguez, Julio
Banga, Julio R.
dc.subject.por.fl_str_mv Science & Technology
topic Science & Technology
description Signaling pathways play a key role in complex diseases such as cancer, for which the development of novel therapies is a difficult, expensive and laborious task. Computational models that can predict the effect of a new combination of drugs without having to test it experimentally can help in accelerating this process. In particular, network-based dynamic models of these pathways hold promise to both understand and predict the effect of therapeutics. However, their use is currently hampered by limitations in our knowledge of the underlying biochemistry, as well as in the experimental and computational technologies used for calibrating the models. Thus, the results from such models need to be carefully interpreted and used in order to avoid biased predictions. Here we present a procedure that deals with this uncertainty by using experimental data to build an ensemble of dynamic models. The method incorporates steps to reduce overfitting and maximize predictive capability. We find that by combining the outputs of individual models in an ensemble it is possible to obtain a more robust prediction. We report results obtained with this method, which we call SELDOM (enSEmbLe of Dynamic lOgic-based Models), showing that it improves the predictions previously reported for several challenging problems.
publishDate 2017
dc.date.none.fl_str_mv 2017-02-06
2017-02-06T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/47805
url http://hdl.handle.net/1822/47805
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 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. PLoS Computational Biology, 13(2), 1-25, 2017
1553-734X
1553-7358
10.1371/journal.pcbi.1005379
28166222
http://journals.plos.org/ploscompbiol/
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Public Library of Science (PLOS)
publisher.none.fl_str_mv Public Library of Science (PLOS)
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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