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Dynamical modeling and analysis of large cellular regulatory networks

dc.contributor.authorBérenguier, D.
dc.contributor.authorChaouiya, C.
dc.contributor.authorMonteiro, P. T.
dc.contributor.authorNaldi, A.
dc.contributor.authorRemy, E.
dc.contributor.authorThieffry, D.
dc.contributor.authorTichit, L.
dc.date.accessioned2015-10-22T14:59:01Z
dc.date.available2015-10-22T14:59:01Z
dc.date.issued2013-06-25
dc.description.abstractThe dynamical analysis of large biological regulatory networks requires the development of scalable methods for mathematical modeling. Following the approach initially introduced by Thomas, we formalize the interactions between the components of a network in terms of discrete variables, functions, and parameters. Model simulations result in directed graphs, called state transition graphs. We are particularly interested in reachability properties and asymptotic behaviors, which correspond to terminal strongly connected components (or "attractors") in the state transition graph. A well-known problem is the exponential increase of the size of state transition graphs with the number of network components, in particular when using the biologically realistic asynchronous updating assumption. To address this problem, we have developed several complementary methods enabling the analysis of the behavior of large and complex logical models: (i) the definition of transition priority classes to simplify the dynamics; (ii) a model reduction method preserving essential dynamical properties, (iii) a novel algorithm to compact state transition graphs and directly generate compressed representations, emphasizing relevant transient and asymptotic dynamical properties. The power of an approach combining these different methods is demonstrated by applying them to a recent multilevel logical model for the network controlling CD4+ T helper cell response to antigen presentation and to a dozen cytokines. This model accounts for the differentiation of canonical Th1 and Th2 lymphocytes, as well as of inflammatory Th17 and regulatory T cells, along with many hybrid subtypes. All these methods have been implemented into the software GINsim, which enables the definition, the analysis, and the simulation of logical regulatory graphs.pt_PT
dc.description.sponsorshipEU FP7 (APOSYS large scale project), EU EraSysBio+ program (project ModHeart), ANR (Project Grant ANR-08-SYSC-003), Belgian Science Policy Office (IAP BioMaGNet).pt_PT
dc.identifier10.1063/1.4809783
dc.identifier.citationChaos 23 , 025114 (2013); doi: 10.1063/1.4809783pt_PT
dc.identifier.doi10.1063/1.4809783
dc.identifier.urihttp://hdl.handle.net/10400.7/427
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherAIP Publishingpt_PT
dc.relationMALIN: Modular modelling and Analysis of Large biological Interacting Networks
dc.relation.publisherversionhttp://scitation.aip.org/content/aip/journal/chaos/23/2/10.1063/1.4809783pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectAttractorspt_PT
dc.subjectNumerical modelingpt_PT
dc.subjectTemporal logicpt_PT
dc.subjectNetworkspt_PT
dc.subjectExplosionspt_PT
dc.titleDynamical modeling and analysis of large cellular regulatory networkspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleMALIN: Modular modelling and Analysis of Large biological Interacting Networks
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FEIA-CCO%2F099229%2F2008/PT
oaire.citation.issue2pt_PT
oaire.citation.titleChaospt_PT
oaire.citation.volume23pt_PT
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication820042aa-3860-49b5-9f01-646a11e76442
relation.isProjectOfPublication.latestForDiscovery820042aa-3860-49b5-9f01-646a11e76442

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