Mathematical analysis and dynamic active subspaces for a long term model of HIV
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Publication:504667
DOI10.3934/MBE.2017040zbMATH Open1366.92126arXiv1604.04588OpenAlexW2963257046WikidataQ40370056 ScholiaQ40370056MaRDI QIDQ504667FDOQ504667
Authors: Tyson Loudon, Stephen Pankavich
Publication date: 17 January 2017
Published in: Mathematical Biosciences and Engineering (Search for Journal in Brave)
Abstract: Recently, a long-term model of HIV infection dynamics was developed to describe the entire time course of the disease. It consists of a large system of ODEs with many parameters, and is expensive to simulate. In the current paper, this model is analyzed by determining all infection-free steady states and studying the local stability properties of the unique biologically-relevant equilibrium. Active subspace methods are then used to perform a global sensitivity analysis and study the dependence of an infected individual's T-cell count on the parameter space. Building on these results, a global-in-time approximation of the T-cell count is created by constructing dynamic active subspaces and reduced order models are generated, thereby allowing for inexpensive computation.
Full work available at URL: https://arxiv.org/abs/1604.04588
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Cited In (8)
- Three-stage modeling of HIV infection and implications for antiretroviral therapy
- A delayed HIV infection model with the homeostatic proliferation of CD\(4^+\) T cells
- Bistable dynamics and Hopf bifurcation in a refined model of early stage HIV infection
- Data-driven polynomial ridge approximation using variable projection
- Dynamical analysis of a delayed HIV virus dynamic model with cell-to-cell transmission and apoptosis of bystander cells
- On the Deep Active-Subspace Method
- Title not available (Why is that?)
- Global sensitivity analysis of plasma instabilities via active subspaces
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