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Spatial process models are widely used for modeling point-referenced variables arising from diverse scientific domains. Analyzing the resulting random surface provides deeper insights into the nature of latent dependence within the studied response. We develop Bayesian modeling and inference for rapid changes on the response surface to assess directional curvature along a given trajectory. Such trajectories or curves of rapid change, often referred to as wombling boundaries, occur in geographic space in the form of rivers in a flood plain, roads, mountains or plateaus or other topographic features leading to high gradients on the response surface. We demonstrate fully model based Bayesian inference on directional curvature processes to analyze differential behavior in responses along wombling boundaries. We illustrate our methodology with a number of simulated experiments followed by multiple applications featuring the Boston Housing data; Meuse river data; and temperature data from the Northeastern United States. Supplementary materials for this article are available online. 

The majority of Americans fail to achieve recommended levels of physical activity, which leads to numerous preventable health problems, such as diabetes, hypertension, and heart diseases. This has generated substantial interest in monitoring human activity to gear interventions toward environmental features that may relate to higher physical activity. Wearable devices, such as wrist-worn sensors that monitor gross motor activity (actigraph units) continuously record the activity levels of a subject, producing massive amounts of high-resolution measurements. Analyzing actigraph data needs to account for spatial and temporal information on trajectories or paths traversed by subjects wearing such devices. Inferential objectives include estimating a subject’s physical activity levels along a given trajectory, identifying trajectories that are more likely to produce higher levels of physical activity for a given subject, and predicting expected levels of physical activity in any proposed new trajectory for a given set of health attributes. Here, we devise a Bayesian hierarchical modeling framework for spatial-temporal actigraphy data to deliver fully model-based inference on trajectories while accounting for subject-level health attributes and spatial-temporal dependencies. We undertake a comprehensive analysis of an original dataset from the Physical Activity through Sustainable Transport Approaches in Los Angeles (PASTA-LA) study to ascertain spatial zones and trajectories exhibiting significantly higher levels of physical activity while accounting for various sources of heterogeneity. 

Graphical models have witnessed significant growth and usage in spatial data science for modeling data referenced over a massive number of spatial-temporal coordinates. Much of this literature has focused on a single or relatively few spatially dependent outcomes. Recent attention has focused upon addressing modeling and inference for substantially large number of outcomes. While spatial factor models and multivariate basis expansions occupy a prominent place in this domain, this article elucidates a recent approach, graphical Gaussian Processes, that exploits the notion of conditional independence among a very large number of spatial processes to build scalable graphical models for fully model-based Bayesian analysis of multivariate spatial data. 

Spatial probit generalized linear mixed models (spGLMM) with a linear fixed effect and a spatial random effect, endowed with a Gaussian Process prior, are widely used for analysis of binary spatial data. However, the canonical Bayesian implementation of this hierarchical mixed model can involve protracted Markov Chain Monte Carlo sampling. Alternate approaches have been proposed that circumvent this by directly representing the marginal likelihood from spGLMM in terms of multivariate normal cummulative distribution functions (cdf). We present a direct and fast rendition of this latter approach for predictions from a spatial probit linear mixed model. We show that the covariance matrix of the cdf characterizing the marginal cdf of binary spatial data from spGLMM is amenable to approximation using Nearest Neighbor Gaussian Processes (NNGP). This facilitates a scalable prediction algorithm for spGLMM using NNGP that only involves sparse or small matrix computations and can be deployed in an embarrassingly parallel manner. We demonstrate the accuracy and scalability of the algorithm via numerous simulation experiments and an analysis of species presence-absence data. 

Community-based public health interventions often rely on representative, spatially referenced outcome data to draw conclusions about a finite population. To estimate finite-population parameters, we are posed with two challenges: to correctly account for spatial association among the sampled and nonsampled participants and to correctly model missingness in key covariates, which may be also spatially associated. To accomplish this, we take inspiration from the preferential sampling literature and develop a general Bayesian framework that can specifically account for preferential non-response. This framework is first applied to three missing data scenarios in a simulation study. It is then used to account for missing data patterns seen in reported annual household income in a corner-store intervention project. Through this, we are able to construct finite-population estimates of the percent of income spent on fruits and vegetables. Such a framework provides a flexible way to account for spatial association and complex missing data structures in finite populations.

 

Regional aggregates of health outcomes over delineated administrative units (e.g., states, counties, and zip codes), or areal units, are widely used by epidemiologists to map mortality or incidence rates and capture geographic variation. To capture health disparities over regions, we seek “difference boundaries” that separate neighboring regions with significantly different spatial effects. Matters are more challenging with multiple outcomes over each unit, where we capture dependence among diseases as well as across the areal units. Here, we address multivariate difference boundary detection for correlated diseases. We formulate the problem in terms of Bayesian pairwise multiple comparisons and seek the posterior probabilities of neighboring spatial effects being different. To achieve this, we endow the spatial random effects with a discrete probability law using a class of multivariate areally referenced Dirichlet process models that accommodate spatial and interdisease dependence. We evaluate our method through simulation studies and detect difference boundaries for multiple cancers using data from the Surveillance, Epidemiology, and End Results Program of the National Cancer Institute.