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ASPASIA: A toolkit for evaluating the effects of biological interventions on SBML model behaviour.
Evans, Stephanie; Alden, Kieran; Cucurull-Sanchez, Lourdes; Larminie, Christopher; Coles, Mark C; Kullberg, Marika C; Timmis, Jon.
Afiliação
  • Evans S; York Computational Immunology Lab, University of York, York, United Kingdom.
  • Alden K; Centre for Immunology and Infection, Department of Biology and Hull York Medical School, University of York, York, United Kingdom.
  • Cucurull-Sanchez L; Department of Electronics, University of York, York, United Kingdom.
  • Larminie C; York Computational Immunology Lab, University of York, York, United Kingdom.
  • Coles MC; Department of Electronics, University of York, York, United Kingdom.
  • Kullberg MC; GSK Medicines Research Centre, Stevenage, United Kingdom.
  • Timmis J; GSK Medicines Research Centre, Stevenage, United Kingdom.
PLoS Comput Biol ; 13(2): e1005351, 2017 02.
Article em En | MEDLINE | ID: mdl-28158307
ABSTRACT
A calibrated computational model reflects behaviours that are expected or observed in a complex system, providing a baseline upon which sensitivity analysis techniques can be used to analyse pathways that may impact model responses. However, calibration of a model where a behaviour depends on an intervention introduced after a defined time point is difficult, as model responses may be dependent on the conditions at the time the intervention is applied. We present ASPASIA (Automated Simulation Parameter Alteration and SensItivity Analysis), a cross-platform, open-source Java toolkit that addresses a key deficiency in software tools for understanding the impact an intervention has on system behaviour for models specified in Systems Biology Markup Language (SBML). ASPASIA can generate and modify models using SBML solver output as an initial parameter set, allowing interventions to be applied once a steady state has been reached. Additionally, multiple SBML models can be generated where a subset of parameter values are perturbed using local and global sensitivity analysis techniques, revealing the model's sensitivity to the intervention. To illustrate the capabilities of ASPASIA, we demonstrate how this tool has generated novel hypotheses regarding the mechanisms by which Th17-cell plasticity may be controlled in vivo. By using ASPASIA in conjunction with an SBML model of Th17-cell polarisation, we predict that promotion of the Th1-associated transcription factor T-bet, rather than inhibition of the Th17-associated transcription factor RORγt, is sufficient to drive switching of Th17 cells towards an IFN-γ-producing phenotype. Our approach can be applied to all SBML-encoded models to predict the effect that intervention strategies have on system behaviour. ASPASIA, released under the Artistic License (2.0), can be downloaded from http//www.york.ac.uk/ycil/software.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Linguagens de Programação / Software / Biologia de Sistemas / Modelos Biológicos Tipo de estudo: Prognostic_studies Idioma: En Revista: PLoS Comput Biol Assunto da revista: BIOLOGIA / INFORMATICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Linguagens de Programação / Software / Biologia de Sistemas / Modelos Biológicos Tipo de estudo: Prognostic_studies Idioma: En Revista: PLoS Comput Biol Assunto da revista: BIOLOGIA / INFORMATICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido