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It is shown that this model has simulated the temperature distribution very well.
Once the model has simulated all patients until death, outcomes (ie, costs and survival) are summed for the entire cohort.
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Higher-resolution models have simulated more realistic TC climatology (Walsh et al. 2016).
From these SFN and Alamouti MISO channel equation models, we have simulated the path gain of the different reception case studies.
Fewer models though have simulated the events following diagnosis and treatment of CRC in order to compare postsurgical surveillance strategies [ 34- 37].
In order to prove the validity of our model, we have simulated the measurement of reactive power and energy.
In order to validate the results obtained from the model, we have simulated the same scenario in MATLAB.
For our epidermal model, we have simulated the cell shape and movement actions on the same time scale as the intracellular gene network.
We have simulated the model with a larger number of samples, i.e., N = L = 1000.
In each model, we have simulated systems in which the amount of telomere lost is fixed, or is length-dependent; cases where cells/chromosomes divide whenever possible, or when there is a probability of division which depends on telomere length.
The proposed model has been simulated by using CST Microwave Studio a commercially available simulator based on finite integral technique and similar result has been obtained.
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