RESUMO
In stochastic models of chemically reacting systems that contain bimolecular reactions, the dynamics of the moments of order up to n of the species populations do not form a closed system, in the sense that their time-derivatives depend on moments of order n + 1. To close the dynamics, the moments of order n + 1 are generally approximated by nonlinear functions of the lower order moments. If the molecule counts of some of the species have a high probability of becoming zero, such approximations may lead to imprecise results and stochastic simulation is the only viable alternative for system analysis. Stochastic simulation can produce exact realizations of chemically reacting systems, but tends to become computationally expensive, especially for stiff systems that involve reactions at different time scales. Further, in some systems, important stochastic events can be very rare and many simulations are necessary to obtain accurate estimates. The computational cost of stochastic simulation can then be prohibitively large. In this paper, we propose a novel method for estimating the moments of chemically reacting systems. The method is based on closing the moment dynamics by replacing the moments of order n + 1 by estimates calculated from a small number of stochastic simulation runs. The resulting stochastic system is then used in an extended Kalman filter, where estimates of the moments of order up to n, obtained from the same simulation, serve as outputs of the system. While the initial motivation for the method was improving over the performance of stochastic simulation and moment closure methods, we also demonstrate that it can be used in an experimental setting to estimate moments of species that cannot be measured directly from time course measurements of the moments of other species.
