Experimental design for dynamics identification of cellular processes
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Abstract: We address the problem of using nonlinear models to design experiments to characterize the dynamics of cellular processes by using the approach of the Maximally Informative Next Experiment (MINE), which was introduced in [W. Dong, et al. Systems biology of the clock in neurospora crassa. {em PLoS ONE}, page e3105, 2008] and independently in [M. M. Donahue, et al. Experiment design through dynamical characterization of non-linear systems biology models utilising sparse grids. {em IET System Biology}, 4:249--262, 2010]. In this approach, existing data is used to define a probability distribution on the parameters; the next measurement point is the one that yields the largest model output variance with this distribution. Building upon this approach, we introduce the Expected Dynamics Estimator (EDE), which is the expected value using this distribution of the output as a function of time. We prove the consistency of this estimator (uniform convergence to true dynamics) even when the chosen experiments cluster in a finite set of points. We extend this proof of consistency to various practical assumptions on noisy data and moderate levels of model mismatch. Through the derivation and proof, we develop a relaxed version of MINE that is more computationally tractable and robust than the original formulation. The results are illustrated with numerical examples on two nonlinear ordinary differential equation models of biomolecular and cellular processes.
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Cited in
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- Evaluating the efficiency of cell mechanisms and systems
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- Convergence of Griddy Gibbs sampling and other perturbed Markov chains
- D-optimal input design for nonlinear FIR-type systems: a dispersion-based approach
- Identifiability and observability analysis for experimental design in nonlinear dynamical models
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