Deterministic approximate inference techniques for conditionally Gaussian state space models

We describe a novel deterministic approximate inference technique for conditionally Gaussian state space models, i.e. state space models where the latent state consists of both multinomial and Gaussian distributed variables. The method can be interpreted as a smoothing pass and iteration scheme symmetric to an assumed density filter. It improves upon previously proposed smoothing passes by not making more approximations than implied by the projection onto the chosen parametric form, the assumed density. Experimental results show that the novel scheme outperforms these alternative deterministic smoothing passes. Comparisons with sampling methods suggest that the performance does not degrade with longer sequences.     

Learning causal structure from mixed data with missing values using Gaussian copula models

We consider the problem of causal structure learning from data with missing values, assumed to be drawn from a Gaussian copula model. First, we extend the ‘Rank PC’ algorithm, designed for Gaussian copula models with purely continuous data (so-called nonparanormal models), to incomplete data by applying rank correlation to pairwise complete observations and replacing the sample size with an effective sample size in the conditional independence tests to account for the information loss from missing values. When the data are missing completely at random (MCAR), we provide an error bound on the accuracy of ‘Rank PC’ and show its high-dimensional consistency. However, when the data are missing at random (MAR), ‘Rank PC’ fails dramatically. Therefore, we propose a Gibbs sampling procedure to draw correlation matrix samples from mixed data that still works correctly under MAR. These samples are translated into an average correlation matrix and an effective sample size, resulting in the ‘Copula PC’ algorithm for incomplete data. Simulation study shows that: (1) ‘Copula PC’ estimates a more accurate correlation matrix and causal structure than ‘Rank PC’ under MCAR and, even more so, under MAR and (2) the usage of the effective sample size significantly improves the performance of ‘Rank PC’ and ‘Copula PC.’ We illustrate our methods on two real-world datasets: riboflavin production data and chronic fatigue syndrome data.