5,370 research outputs found
Evaluation of HIV infected Cells
In this paper, Human Immunodeficiency Virus (HIV) infected cells is found out using a Simulink model. The Simulink solution is equivalent or very close to the exact solution of the problem. Accuracy of the Simulink solution to this problem is better than the existing numerical methods. The main advantage of Simulink model is that solution of any dynamicalproblem can be obtained by anybody without writing any codes. Anillustrative numerical example is presented for the proposed method
Numerical investigation of Differential Biological-Models via GA-Kansa Method Inclusive Genetic Strategy
In this paper, we use Kansa method for solving the system of differential
equations in the area of biology. One of the challenges in Kansa method is
picking out an optimum value for Shape parameter in Radial Basis Function to
achieve the best result of the method because there are not any available
analytical approaches for obtaining optimum Shape parameter. For this reason,
we design a genetic algorithm to detect a close optimum Shape parameter. The
experimental results show that this strategy is efficient in the systems of
differential models in biology such as HIV and Influenza. Furthermore, we prove
that using Pseudo-Combination formula for crossover in genetic strategy leads
to convergence in the nearly best selection of Shape parameter.Comment: 42 figures, 23 page
Estimation of constant and time-varying dynamic parameters of HIV infection in a nonlinear differential equation model
Modeling viral dynamics in HIV/AIDS studies has resulted in a deep
understanding of pathogenesis of HIV infection from which novel antiviral
treatment guidance and strategies have been derived. Viral dynamics models
based on nonlinear differential equations have been proposed and well developed
over the past few decades. However, it is quite challenging to use experimental
or clinical data to estimate the unknown parameters (both constant and
time-varying parameters) in complex nonlinear differential equation models.
Therefore, investigators usually fix some parameter values, from the literature
or by experience, to obtain only parameter estimates of interest from clinical
or experimental data. However, when such prior information is not available, it
is desirable to determine all the parameter estimates from data. In this paper
we intend to combine the newly developed approaches, a multi-stage
smoothing-based (MSSB) method and the spline-enhanced nonlinear least squares
(SNLS) approach, to estimate all HIV viral dynamic parameters in a nonlinear
differential equation model. In particular, to the best of our knowledge, this
is the first attempt to propose a comparatively thorough procedure, accounting
for both efficiency and accuracy, to rigorously estimate all key kinetic
parameters in a nonlinear differential equation model of HIV dynamics from
clinical data. These parameters include the proliferation rate and death rate
of uninfected HIV-targeted cells, the average number of virions produced by an
infected cell, and the infection rate which is related to the antiviral
treatment effect and is time-varying. To validate the estimation methods, we
verified the identifiability of the HIV viral dynamic model and performed
simulation studies.Comment: Published in at http://dx.doi.org/10.1214/09-AOAS290 the Annals of
Applied Statistics (http://www.imstat.org/aoas/) by the Institute of
Mathematical Statistics (http://www.imstat.org
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