This problem is usually addressed by fitting model simulations to the observed experimental dataset (ob(i inmathbb{R}^{n}), (i=1,ldots,K).
To assess the properties of the model, we first examine its ability to reproduce the basic features of labor force participation and employment observed in our sample by comparing model simulations to observed data.
However, the elements of and S cannot be estimated by comparing model simulations to data, as the generated state trajectories are different for each simulation of the SDE model.
The accuracy of the constructed model was determined by comparing the results of model simulations to experimental results for growth on cellobiose and fructose from two different independent studies.
Nonlinear buckling of elastic thin films on compliant substrates is studied by modeling and simulations to reveal the roles of pre-strain, elastic modulus ratio, and interfacial properties in morphological transition from wrinkles to buckle-delamination blisters.
Furthermore, the solutions obtained by using those methods or the strategies inferred by model simulations need to be validated before the implementation in the laboratory, because of model uncertainties.
The action potential of the designed RGCs and the ionic currents are measured by the model simulation to analyse the effect of different types of Calcium currents and gap junction conductances in RGC apoptosis.
Estimation of fTR is conducted by comparing model-based simulations to observed data from mass balance studies.
The synthesis rates, v X, activation rates, v i, degradation rates, d X, and coefficients K i are determined by fitting the model simulation to experimental data from human Jurkat cells treated with 100ng/mol FasL (Fig. 3).
Finally, by adding a visualization model to the simulation and by editing this model, we can confirm that the HLA interface can provide user-friendly functions such as adding new model and editing a model.
