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In the model developed, we analyse, how the interactions between the agents lead to various ideological scenarios.
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For this reason we followed a 10-fold cross validation procedure [25] for each one of the individual models developed: we randomly divided the initial dataset into 10 equal subsets.
Until the ideal preclinical model is developed, we need to work with our less-than-perfect animal models.
Using the model we developed, we obtained an excellent fit to sensor glucose in most individuals.
Once the model was developed, we excluded the 17 (0.6%) patients with missing data in the selected predictors from the analysis.
Using a decision model we developed, we estimate that among children, vaccination would saved 1.9 quality-adjusted life days (QALD) and $33 per person.
As newer models are developed we hope to use this data set to evaluate them.
In the model developed below, we expand the behavioral response repertoire of agents infected with fear to include both flight and protective self-isolation.
Yet in the model developed here, we suggest that restricted pleiotropy emerges to expand the range of accessible combinations of phenotypes.
Consistent with this working model developed in other fungi, we demonstrated that the PMT2 gene is essential for viability in C. neoformans.
To further assess the models developed herein, we investigated the influence of patient background.
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