Abstract
The inference of reaction rate parameters in biochemical network models from time series concentration data is a central task in computational systems biology. Under the assumption of well mixed conditions the network dynamics are typically described by the chemical master equation, the Fokker Planck equation, the linear noise approximation or the macroscopic rate equation. The inverse problem of estimating the parameters of the underlying network model can be approached in deterministic and stochastic ways, and available methods often compare individual or mean concentration traces obtained from experiments with theoretical model predictions when maximizing likelihoods, minimizing regularized least squares functionals, approximating posterior distributions or sequentially processing the data. In this article we assume that the biological reaction network can be observed at least partially and repeatedly over time such that sample moments of species molecule numbers for various time points can be calculated from the data. Based on the chemical master equation we furthermore derive closed systems of parameter dependent nonlinear ordinary differential equations that predict the time evolution of the statistical moments. For inferring the reaction rate parameters we suggest to not only compare the sample mean with the theoretical mean prediction but also to take the residual of higher order moments explicitly into account. Cost functions that involve residuals of higher order moments may form landscapes in the parameter space that have more pronounced curvatures at the minimizer and hence may weaken or even overcome parameter sloppiness and uncertainty. As a consequence both deterministic and stochastic parameter inference algorithms may be improved with respect to accuracy and efficiency. We demonstrate the potential of moment fitting for parameter inference by means of illustrative stochastic biological models from the literature and address topics for future research.
Highlights
The traditional approach to modelling of biological reaction networks is based on deterministic mass action kinetics in which the time course of the species concentrations averaged over the population is described by a set of coupled ordinary differential equations [1], often referred to as the macroscopic rate equations
In well-mixed conditions the system dynamics are captured by the Kolmogorov differential equation, referred to as the chemical master equation, for the transition probability kernel of a continuous time Markov process with discrete state space
An alternative approximative description is the linear noise approximation [6] that features a partial differential equation for the probability distribution of the fluctuations around the deterministic part governed by the macroscopic rate equation
Summary
The traditional approach to modelling of biological reaction networks is based on deterministic mass action kinetics in which the time course of the species concentrations averaged over the population is described by a set of coupled ordinary differential equations [1], often referred to as the macroscopic rate equations. For the description of intra-cellular processes characterized by a low number of reacting molecules the stochastic modelling approach [2] is an alternative that explicitly takes the discreteness and stochasticity of chemical kinetics into account. In well-mixed conditions the system dynamics are captured by the Kolmogorov differential equation, referred to as the chemical master equation, for the transition probability kernel of a continuous time Markov process with discrete state space. An alternative approximative description is the linear noise approximation [6] that features a partial differential equation for the probability distribution of the fluctuations around the deterministic part governed by the macroscopic rate equation
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