Journal article icon

Journal article

ASPASIA: A toolkit for evaluating the effects of biological interventions on SBML model behaviour

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.
Publication status:
Published
Peer review status:
Peer reviewed

Actions


Access Document


Publisher copy:
10.1371/journal.pcbi.1005351

Authors


More by this author
Role:
Author
ORCID:
0000-0002-2345-5249
More by this author
Role:
Author
ORCID:
0000-0003-4411-1776
More by this author
Role:
Author
ORCID:
0000-0002-2397-6490
More by this author
Role:
Author
ORCID:
0000-0003-4986-1824
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Kennedy Institute for Rheumatology
Role:
Author

Contributors

Role:
Editor


Publisher:
Public Library of Science
Journal:
PLoS Computational Biology More from this journal
Volume:
13
Issue:
2
Pages:
e1005351
Publication date:
2017-02-03
Acceptance date:
2017-01-08
DOI:
EISSN:
1553-7358
ISSN:
1553-734X
Pmid:
28158307


Language:
English
Keywords:
Pubs id:
pubs:821761
UUID:
uuid:9572a716-e758-4750-9224-a48044e3b42c
Local pid:
pubs:821761
Source identifiers:
821761
Deposit date:
2018-05-17

Terms of use



Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP