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We consider Bayesian inference for stochastic differential equation mixed effects models (SDEMEMs) exemplifying tumor response to treatment and regrowth in mice. We produce an extensive study on how a SDEMEM can be fitted using both exact inference based on pseudo-marginal MCMC and approximate inference via Bayesian synthetic likelihoods (BSL). We investigate a two-compartments SDEMEM, these corresponding to the fractions of tumor cells killed by and survived to a treatment, respectively. Case study data considers a tumor xenography study with two treatment groups and one control, each containing 5-8 mice. Results from the case study and from simulations indicate that the SDEMEM is able to reproduce the observed growth patterns and that BSL is a robust tool for inference in SDEMEMs. Finally, we compare the fit of the SDEMEM to a similar ordinary differential equation model. Due to small sample sizes, strong prior information is needed to identify all model parameters in the SDEMEM and it cannot be determined which of the two models is the better in terms of predicting tumor growth curves. In a simulation study we find that with a sample of 17 mice per group BSL is able to identify all model parameters and distinguish treatment groups.
Stochastic differential equations (SDEs) are established tools to model physical phenomena whose dynamics are affected by random noise. By estimating parameters of an SDE intrinsic randomness of a system around its drift can be identified and separat
We consider the problem of selecting deterministic or stochastic models for a biological, ecological, or environmental dynamical process. In most cases, one prefers either deterministic or stochastic models as candidate models based on experience or
Stochastic differential equation mixed-effects models (SDEMEMs) are flexible hierarchical models that are able to account for random variability inherent in the underlying time-dynamics, as well as the variability between experimental units and, opti
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We use the theory of normal variance-mean mixtures to derive a data augmentation scheme for models that include gamma functions. Our methodology applies to many situations in statistics and machine learning, including Multinomial-Dirichlet distributi