We derive and present explicit algorithms to facilitate streamlined computing for variational inference for models containing higher level random effects. Existing literature is such that streamlined variational inference is restricted to mean field variational Bayes algorithms for two-level random effects models. Here we provide the following extensions: (1) explicit Gaussian response mean field variational Bayes algorithms for three-level models, (2) explicit algorithms for the alternative variational message passing approach in the case of two-level and three-level models, and (3) an explanation of how arbitrarily high levels of nesting can be handled based on the recently published matrix algebraic results of the authors. A pay-off from (2) is simple extension to non-Gaussian response models. In summary, we remove barriers for streamlining variational inference algorithms based on either the mean field variational Bayes approach or the variational message passing approach when higher level random effects are present.

We introduce the term semiparametric mean field variational Bayes to describe the relaxation of mean field variational Bayes in which some density functions in the product density restriction are pre-specified to be members of convenient parametric families. This notion has appeared in various guises in the mean field variational Bayes literature during its history and we endeavor to unify this important topic. We lay down a general framework and explain how previous relevant methodologies fall within this framework. A major contribution is elucidation of numerical issues that impact semiparametric mean field variational Bayes in practice.

BACKGROUND: High-throughput flow cytometry experiments produce hundreds of large multivariate samples of cellular characteristics. These samples require specialized processing to obtain clinically meaningful measurements. A major component of this processing is a form of cell subsetting known as gating. Manual gating is time-consuming and subjective. Good automatic and semi-automatic gating algorithms are very beneficial to high-throughput flow cytometry. RESULTS: We develop a statistical procedure, named curvHDR, for automatic and semi-automatic gating. The method combines the notions of significant high negative curvature regions and highest density regions and has the ability to adapt well to human-perceived gates. The underlying principles apply to dimension of arbitrary size, although we focus on dimensions up to three. Accompanying software, compatible with contemporary flow cytometry infor-matics, is developed. CONCLUSION: The method is seen to adapt well to nuances in the data and, to a reasonable extent, match human perception of useful gates. It offers big savings in human labour when processing high-throughput flow cytometry data whilst retaining a good degree of efficacy.