| Literature DB >> 28395655 |
Piero Dalle Pezze1, Nicolas Le Novère2.
Abstract
BACKGROUND: The rapid growth of the number of mathematical models in Systems Biology fostered the development of many tools to simulate and analyse them. The reliability and precision of these tasks often depend on multiple repetitions and they can be optimised if executed as pipelines. In addition, new formal analyses can be performed on these repeat sequences, revealing important insights about the accuracy of model predictions.Entities:
Keywords: Modelling; Parameter estimation; Pipeline; Simulation
Mesh:
Year: 2017 PMID: 28395655 PMCID: PMC5387271 DOI: 10.1186/s12918-017-0423-3
Source DB: PubMed Journal: BMC Syst Biol ISSN: 1752-0509
Fig. 1Implemented pipelines in SBpipe. a Example of work flow using the parameter estimation pipeline. Parameter estimations were performed using data sets of different sizes. The Identifiable column shows the results using a data set sufficient for estimating the parameters with their confidence intervals, whereas the column Non-identifiable illustrates the results using the same model but a reduced data set, insufficient for identifying parameter values. Size of the fit sequence: N=1000. For the complete results generated by this pipeline, see Additional file 1: Tables S2–S4, Figures S2–S8. b Deterministic and stochastic model time courses for the phosphorylated IR_beta species obtained with the model simulation pipeline. For stochastic simulations, mean (black), 95% confidence interval for the mean (cyan), and 1 standard deviation (light blue) are reported. Experimental data are added and indicated as red circles. For the complete results, see Additional file 1: Figures S9–S10. c Single parameter scan pipeline. The k1 parameter regulating the IR_beta phosphorylation was scanned within its 95% estimated confidence interval. The blue area is the results of 100 time course simulations over this interval. For the complete results, see Additional file 1: Figures S11–S12. d Double parameter scan pipeline. Signal intensities for the phosphorylated IR_beta receptor different levels of Insulin (x axis) and IR_beta receptor (y axis) at 1, 2, 5, and 10 minutes upon insulin stimulation. The colour representation indicates how the readout signal intensity varies upon two model parameter levels. For the complete results, see Additional file 1: Figures S13–S15. All the results can be replicated using the test files provided within the SBpipe package available online on the GitHub repository