65-XX NUMERICAL ANALYSIS
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One of the main goals of mathematical modelling in systems biology related to medical applications is to obtain patient-specific parameterisations and model predictions.
In clinical practice, however, the number of available measurements for single patients is usually limited due to time and cost restrictions. This hampers the process of making patient-specific predictions about the outcome of a treatment. On the other hand, data are often available for many patients, in particular if extensive clinical studies have been performed. Using these population data, we propose an iterative algorithm for contructing an informative prior distribution, which then serves as the basis for computing patient-specific posteriors and obtaining individual predictions. We demonsrate the performance of our method by applying it to a low-dimensional parameter estimation problem in a toy model as well as to a high-dimensional ODE model of the human menstrual cycle, which represents a typical example from systems biology modelling.
A deterministic model of tuberculosis in sub-Saharan Africa in general and Cameroon in particular including lack of access to the treatment and weak diagnose capacity is designed and analyzed with respect to its transmission dynamics.
The model includes both frequency- and density-dependent transmissions. It is shown that the model is mathematically well-posed and epidemiologically reasonable. Solutions are non-negative and bounded whenever the initial values are non-negative.
A sensitivity analysis of model parameters is performed and most sensitive parameters of the model are identified using a state-of-the-art Gauss-Newton
Method. In particular, parameters representing the proportion of individuals having access to medical facilities have a large impact on the dynamics of the disease. It has been shown that an increase of these parameter values over the
time can significantly reduce the disease burden in the population within the next 15 years.
Particle methods have become indispensible in conformation dynamics to
compute transition rates in protein folding, binding processes and
molecular design, to mention a few.
Conformation dynamics requires at a decomposition of a molecule's position
space into metastable conformations.
In this paper, we show how this decomposition
can be obtained via the design of either ``soft'' or ``hard''
molecular conformations.
We show, that the soft approach results in a larger metastabilitiy of
the decomposition and is thus more advantegous. This is illustrated
by a simulation of Alanine Dipeptide.