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The orbital superposition method originally developed by Schwarzschild (1979) is used to study the dynamics of growth of a black hole and its host galaxy, and has uncovered new relationships between the galaxy's global characteristics. Scientists are specifically interested in finding optimal parameter choices for this model that best match physical measurements along with quantifying the uncertainty of such procedures. This renders a statistical calibration problem with multivariate outcomes. In this article, we develop a Bayesian method for calibration with multivariate outcomes using orthogonal bias functions thus ensuring parameter identifiability. Our approach is based on projecting the posterior to an appropriate space which allows the user to choose any nonparametric prior on the bias function(s) instead of having to model it (them) with Gaussian processes. We develop a functional projection approach using the theory of Hilbert spaces. A finite-dimensional analogue of the projection problem is also considered. We illustrate the proposed approach using a BART prior and apply it to calibrate the Schwarzschild model illustrating how a multivariate approach may resolve discrepancies resulting from a univariate calibration.

Sparse training has emerged as a promising method for resource-efficient deep neural networks (DNNs) in real-world applications. However, the reliability of sparse models remains a crucial concern, particularly in detecting unknown out-of-distribution (OOD) data. This study addresses the knowledge gap by investigating the reliability of sparse training from an OOD perspective and reveals that sparse training exacerbates OOD unreliability. The lack of unknown information and the sparse constraints hinder the effective exploration of weight space and accurate differentiation between known and unknown knowledge. To tackle these challenges, we propose a new unknown-aware sparse training method, which incorporates a loss modification, auto-tuning strategy, and a voting scheme to guide weight space exploration and mitigate confusion between known and unknown information without incurring significant additional costs or requiring access to additional OOD data. Theoretical insights demonstrate how our method reduces model confidence when faced with OOD samples. Empirical experiments across multiple datasets, model architectures, and sparsity levels validate the effectiveness of our method, with improvements of up to \textbf{8.4\%} in AUROC while maintaining comparable or higher accuracy and calibration. This research enhances the understanding and readiness of sparse DNNs for deployment in resource-limited applications. Our code is available on: \url{https://github.com/StevenBoys/MOON}.

There is a significant interest in exploring non-linear associations among multiple images derived from diverse imaging modalities. While there is a growing literature on image-on-image regression to delineate predictive inference of an image based on multiple images, existing approaches have limitations in efficiently borrowing information between multiple imaging modalities in the prediction of an image. Building on the literature of Variational Auto Encoders (VAEs), this article proposes a novel approach, referred to as Integrative Variational Autoencoder (\texttt{InVA}) method, which borrows information from multiple images obtained from different sources to draw predictive inference of an image. The proposed approach captures complex non-linear association between the outcome image and input images, while allowing rapid computation. Numerical results demonstrate substantial advantages of \texttt{InVA} over VAEs, which typically do not allow borrowing information between input images. The proposed framework offers highly accurate predictive inferences for costly positron emission topography (PET) from multiple measures of cortical structure in human brain scans readily available from magnetic resonance imaging (MRI).

Thompson sampling (TS) is one of the most popular and earliest algorithms to solve stochastic multi-armed bandit problems. We consider a variant of TS, named $\alpha$-TS, where we use a fractional or $\alpha$-posterior ($\alpha\in(0,1)$) instead of the standard posterior distribution. To compute an $\alpha$-posterior, the likelihood in the definition of the standard posterior is tempered with a factor $\alpha$. For $\alpha$-TS we obtain both instance-dependent $\mathcal{O}\left(\sum_{k \neq i^*} \Delta_k\left(\frac{\log(T)}{C(\alpha)\Delta_k^2} + \frac{1}{2} \right)\right)$ and instance-independent $\mathcal{O}(\sqrt{KT\log K})$ frequentist regret bounds under very mild conditions on the prior and reward distributions, where $\Delta_k$ is the gap between the true mean rewards of the $k^{th}$ and the best arms, and $C(\alpha)$ is a known constant. Both the sub-Gaussian and exponential family models satisfy our general conditions on the reward distribution. Our conditions on the prior distribution just require its density to be positive, continuous, and bounded. We also establish another instance-dependent regret upper bound that matches (up to constants) to that of improved UCB [Auer and Ortner, 2010]. Our regret analysis carefully combines recent theoretical developments in the non-asymptotic concentration analysis and Bernstein-von Mises type results for the $\alpha$-posterior distribution. Moreover, our analysis does not require additional structural properties such as closed-form posteriors or conjugate priors.

In a traditional Gaussian graphical model, data homogeneity is routinely assumed with no extra variables affecting the conditional independence. In modern genomic datasets, there is an abundance of auxiliary information, which often gets under-utilized in determining the joint dependency structure. In this article, we consider a Bayesian approach to model undirected graphs underlying heterogeneous multivariate observations with additional assistance from covariates. Building on product partition models, we propose a novel covariate-dependent Gaussian graphical model that allows graphs to vary with covariates so that observations whose covariates are similar share a similar undirected graph. To efficiently embed Gaussian graphical models into our proposed framework, we explore both Gaussian likelihood and pseudo-likelihood functions. For Gaussian likelihood, a G-Wishart distribution is used as a natural conjugate prior, and for the pseudo-likelihood, a product of Gaussian-conditionals is used. Moreover, the proposed model has large prior support and is flexible to approximate any $\nu$-H\"{o}lder conditional variance-covariance matrices with $\nu\in(0,1]$. We further show that based on the theory of fractional likelihood, the rate of posterior contraction is minimax optimal assuming the true density to be a Gaussian mixture with a known number of components. The efficacy of the approach is demonstrated via simulation studies and an analysis of a protein network for a breast cancer dataset assisted by mRNA gene expression as covariates., Comment: 58 pages, 12 figures, accepted by Journal of the American Statistical Association

Neural processes are a family of probabilistic models that inherit the flexibility of neural networks to parameterize stochastic processes. Despite providing well-calibrated predictions, especially in regression problems, and quick adaptation to new tasks, the Gaussian assumption that is commonly used to represent the predictive likelihood fails to capture more complicated distributions such as multimodal ones. To overcome this limitation, we propose Conditional Quantile Neural Processes (CQNPs), a new member of the neural processes family, which exploits the attractive properties of quantile regression in modeling the distributions irrespective of their form. By introducing an extension of quantile regression where the model learns to focus on estimating informative quantiles, we show that the sampling efficiency and prediction accuracy can be further enhanced. Our experiments with real and synthetic datasets demonstrate substantial improvements in predictive performance compared to the baselines, and better modeling of heterogeneous distributions' characteristics such as multimodality.

Single-cell RNA-sequencing technologies may provide valuable insights to the understanding of the composition of different cell types and their functions within a tissue. Recent technologies such as spatial transcriptomics, enable the measurement of gene expressions at the single cell level along with the spatial locations of these cells in the tissue. Dimension-reduction and spatial clustering are two of the most common exploratory analysis strategies for spatial transcriptomic data. However, existing dimension reduction methods may lead to a loss of inherent dependency structure among genes at any spatial location in the tissue and hence do not provide insights of gene co-expression pattern. In spatial transcriptomics, the matrix-variate gene expression data, along with spatial co-ordinates of the single cells, provides information on both gene expression dependencies and cell spatial dependencies through its row and column covariances. In this work, we propose a flexible Bayesian approach to simultaneously estimate the row and column covariances for the matrix-variate spatial transcriptomic data. The posterior estimates of the row and column covariances provide data summaries for downstream exploratory analysis. We illustrate our method with simulations and two analyses of real data generated from a recent spatial transcriptomic platform. Our work elucidates gene co-expression networks as well as clear spatial clustering patterns of the cells.

With the increasing amount of distributed energy resources (DERs) integration, there is a significant need to model and analyze hosting capacity (HC) for future electric distribution grids. Hosting capacity analysis (HCA) examines the amount of DERs that can be safely integrated into the grid and is a challenging task in full generality because there are many possible integration of DERs in foresight. That is, there are numerous extreme points between feasible and infeasible sets. Moreover, HC depends on multiple factors such as (a) adoption patterns of DERs that depend on socio-economic behaviors and (b) how DERs are controlled and managed. These two factors are intrinsic to the problem space because not all integration of DERs may be centrally planned, and could largely change our understanding about HC. This paper addresses the research gap by capturing the two factors (a) and (b) in HCA and by identifying a few most insightful HC scenarios at the cost of domain knowledge. We propose a data-driven HCA framework and introduce active learning in HCA to effectively explore scenarios. Active learning in HCA and characteristics of HC with respect to the two factors (a) and (b) are illustrated in a 3-bus example. Next, detailed large-scale studies are proposed to understand the significance of (a) and (b). Our findings suggest that HC and its interpretations significantly change subject to the two factors (a) and (b).

Posterior computation in hierarchical Dirichlet process (HDP) mixture models is an active area of research in nonparametric Bayes inference of grouped data. Existing literature almost exclusively focuses on the Chinese restaurant franchise (CRF) analogy of the marginal distribution of the parameters, which can mix poorly and has a quadratic complexity with the sample size. A recently developed slice sampler allows for efficient blocked updates of the parameters, but is shown to be statistically unstable in our article. We develop a blocked Gibbs sampler that employs a truncated approximation of the underlying random measures to sample from the posterior distribution of HDP, which produces statistically stable results, is highly scalable with respect to sample size, and is shown to have good mixing. The heart of the construction is to endow the shared concentration parameter with an appropriately chosen gamma prior that allows us to break the dependence of the shared mixing proportions and permits independent updates of certain log-concave random variables in a block. En route, we develop an efficient rejection sampler for these random variables leveraging piece-wise tangent-line approximations.

Gaussian graphical models typically assume a homogeneous structure across all subjects, which is often restrictive in applications. In this article, we propose a weighted pseudo-likelihood approach for graphical modeling which allows different subjects to have different graphical structures depending on extraneous covariates. The pseudo-likelihood approach replaces the joint distribution by a product of the conditional distributions of each variable. We cast the conditional distribution as a heteroscedastic regression problem, with covariate-dependent variance terms, to enable information borrowing directly from the data instead of a hierarchical framework. This allows independent graphical modeling for each subject, while retaining the benefits of a hierarchical Bayes model and being computationally tractable. An efficient embarrassingly parallel variational algorithm is developed to approximate the posterior and obtain estimates of the graphs. Using a fractional variational framework, we derive asymptotic risk bounds for the estimate in terms of a novel variant of the $\alpha$-R\'{e}nyi divergence. We theoretically demonstrate the advantages of information borrowing across covariates over independent modeling. We show the practical advantages of the approach through simulation studies and illustrate the dependence structure in protein expression levels on breast cancer patients using CNV information as covariates.

Although sparse training has been successfully used in various resource-limited deep learning tasks to save memory, accelerate training, and reduce inference time, the reliability of the produced sparse models remains unexplored. Previous research has shown that deep neural networks tend to be over-confident, and we find that sparse training exacerbates this problem. Therefore, calibrating the sparse models is crucial for reliable prediction and decision-making. In this paper, we propose a new sparse training method to produce sparse models with improved confidence calibration. In contrast to previous research that uses only one mask to control the sparse topology, our method utilizes two masks, including a deterministic mask and a random mask. The former efficiently searches and activates important weights by exploiting the magnitude of weights and gradients. While the latter brings better exploration and finds more appropriate weight values by random updates. Theoretically, we prove our method can be viewed as a hierarchical variational approximation of a probabilistic deep Gaussian process. Extensive experiments on multiple datasets, model architectures, and sparsities show that our method reduces ECE values by up to 47.8\% and simultaneously maintains or even improves accuracy with only a slight increase in computation and storage burden.

We consider the problem of clustering grouped data with possibly non-exchangeable groups whose dependencies can be characterized by a known directed acyclic graph. To allow the sharing of clusters among the non-exchangeable groups, we propose a Bayesian nonparametric approach, termed graphical Dirichlet process, that jointly models the dependent group-specific random measures by assuming each random measure to be distributed as a Dirichlet process whose concentration parameter and base probability measure depend on those of its parent groups. The resulting joint stochastic process respects the Markov property of the directed acyclic graph that links the groups. We characterize the graphical Dirichlet process using a novel hypergraph representation as well as the stick-breaking representation, the restaurant-type representation, and the representation as a limit of a finite mixture model. We develop an efficient posterior inference algorithm and illustrate our model with simulations and a real grouped single-cell dataset.

Despite impressive performance, deep neural networks require significant memory and computation costs, prohibiting their application in resource-constrained scenarios. Sparse training is one of the most common techniques to reduce these costs, however, the sparsity constraints add difficulty to the optimization, resulting in an increase in training time and instability. In this work, we aim to overcome this problem and achieve space-time co-efficiency. To accelerate and stabilize the convergence of sparse training, we analyze the gradient changes and develop an adaptive gradient correction method. Specifically, we approximate the correlation between the current and previous gradients, which is used to balance the two gradients to obtain a corrected gradient. Our method can be used with the most popular sparse training pipelines under both standard and adversarial setups. Theoretically, we prove that our method can accelerate the convergence rate of sparse training. Extensive experiments on multiple datasets, model architectures, and sparsities demonstrate that our method outperforms leading sparse training methods by up to \textbf{5.0\%} in accuracy given the same number of training epochs, and reduces the number of training epochs by up to \textbf{52.1\%} to achieve the same accuracy. Our code is available on: \url{https://github.com/StevenBoys/AGENT}.

Modern data science applications often involve complex relational data with dynamic structures. An abrupt change in such dynamic relational data is typically observed in systems that undergo regime changes due to interventions. In such a case, we consider a factorized fusion shrinkage model in which all decomposed factors are dynamically shrunk towards group-wise fusion structures, where the shrinkage is obtained by applying global-local shrinkage priors to the successive differences of the row vectors of the factorized matrices. The proposed priors enjoy many favorable properties in comparison and clustering of the estimated dynamic latent factors. Comparing estimated latent factors involves both adjacent and long-term comparisons, with the time range of comparison considered as a variable. Under certain conditions, we demonstrate that the posterior distribution attains the minimax optimal rate up to logarithmic factors. In terms of computation, we present a structured mean-field variational inference framework that balances optimal posterior inference with computational scalability, exploiting both the dependence among components and across time. The framework can accommodate a wide variety of models, including dynamic matrix factorization, latent space models for networks and low-rank tensors. The effectiveness of our methodology is demonstrated through extensive simulations and real-world data analysis.

We consider a latent space model for dynamic networks, where our objective is to estimate the pairwise inner products plus the intercept of the latent positions. To balance posterior inference and computational scalability, we consider a structured mean-field variational inference framework, where the time-dependent properties of the dynamic networks are exploited to facilitate computation and inference. Additionally, an easy-to-implement block coordinate ascent algorithm is developed with message-passing type updates in each block, whereas the complexity per iteration is linear with the number of nodes and time points. To certify the optimality, we demonstrate that the variational risk of the proposed variational inference approach attains the minimax optimal rate with only a logarithm factor under certain conditions. To this end, we first derive the minimax lower bound, which might be of independent interest. In addition, we show that the posterior under commonly adopted Gaussian random walk priors can achieve the minimax lower bound with only a logarithm factor. To the best of our knowledge, this is the first such a throughout theoretical analysis of Bayesian dynamic latent space models. Simulations and real data analysis demonstrate the efficacy of our methodology and the efficiency of our algorithm., Comment: Accepted by the Journal of Machine Learning Research http://jmlr.org/papers/v25/22-0514.html

Survival models are used to analyze time-to-event data in a variety of disciplines. Proportional hazard models provide interpretable parameter estimates, but proportional hazards assumptions are not always appropriate. Non-parametric models are more flexible but often lack a clear inferential framework. We propose a Bayesian tree partition model which is both flexible and inferential. Inference is obtained through the posterior tree structure and flexibility is preserved by modeling the the hazard function in each partition using a latent exponentiated Gaussian process. An efficient reversible jump Markov chain Monte Carlo algorithm is accomplished by marginalizing the parameters in each partition element via a Laplace approximation. Consistency properties for the estimator are established. The method can be used to help determine subgroups as well as prognostic and/or predictive biomarkers in time-to-event data. The method is applied to a liver survival dataset and is compared with some existing methods on simulated data.

Clustering of proteins is of interest in cancer cell biology. This article proposes a hierarchical Bayesian model for protein (variable) clustering hinging on correlation structure. Starting from a multivariate normal likelihood, we enforce the clustering through prior modeling using angle based unconstrained reparameterization of correlations and assume a truncated Poisson distribution (to penalize the large number of clusters) as prior on the number of clusters. The posterior distributions of the parameters are not in explicit form and we use a reversible jump Markov chain Monte Carlo (RJMCMC) based technique is used to simulate the parameters from the posteriors. The end products of the proposed method are estimated cluster configuration of the proteins (variables) along with the number of clusters. The Bayesian method is flexible enough to cluster the proteins as well as the estimate the number of clusters. The performance of the proposed method has been substantiated with extensive simulation studies and one protein expression data with a hereditary disposition in breast cancer where the proteins are coming from different pathways.

Causal discovery for purely observational, categorical data is a long-standing challenging problem. Unlike continuous data, the vast majority of existing methods for categorical data focus on inferring the Markov equivalence class only, which leaves the direction of some causal relationships undetermined. This paper proposes an identifiable ordinal causal discovery method that exploits the ordinal information contained in many real-world applications to uniquely identify the causal structure. The proposed method is applicable beyond ordinal data via data discretization. Through real-world and synthetic experiments, we demonstrate that the proposed ordinal causal discovery method combined with simple score-and-search algorithms has favorable and robust performance compared to state-of-the-art alternative methods in both ordinal categorical and non-categorical data. An accompanied R package OrdCD is freely available on CRAN and at https://web.stat.tamu.edu/~yni/files/OrdCD_1.0.0.tar.gz.

We consider the off-policy evaluation (OPE) problem in contextual bandits, where the goal is to estimate the value of a target policy using the data collected by a logging policy. Most popular approaches to the OPE are variants of the doubly robust (DR) estimator obtained by combining a direct method (DM) estimator and a correction term involving the inverse propensity score (IPS). Existing algorithms primarily focus on strategies to reduce the variance of the DR estimator arising from large IPS. We propose a new approach called the Doubly Robust with Information borrowing and Context-based switching (DR-IC) estimator that focuses on reducing both bias and variance. The DR-IC estimator replaces the standard DM estimator with a parametric reward model that borrows information from the 'closer' contexts through a correlation structure that depends on the IPS. The DR-IC estimator also adaptively interpolates between this modified DM estimator and a modified DR estimator based on a context-specific switching rule. We give provable guarantees on the performance of the DR-IC estimator. We also demonstrate the superior performance of the DR-IC estimator compared to the state-of-the-art OPE algorithms on a number of benchmark problems., Comment: 23 pages, 6 figures, manuscript under review

It is well known that the integration among different data-sources is reliable because of its potential of unveiling new functionalities of the genomic expressions which might be dormant in a single source analysis. Moreover, different studies have justified the more powerful analyses of multi-platform data. Toward this, in this study, we consider the circadian genes' omics profile such as copy number changes and RNA sequence data along with their survival response. We develop a Bayesian structural equation modeling coupled with linear regressions and log normal accelerated failure time regression to integrate the information between these two platforms to predict the survival of the subjects. We place conjugate priors on the regression parameters and derive the Gibbs sampler using the conditional distributions of them. Our extensive simulation study shows that the integrative model provides a better fit to the data than its closest competitor. The analyses of glioblastoma cancer data and the breast cancer data from TCGA, the largest genomics and transcriptomics database, support our findings. The developed method is wrapped in R package semmcmc available at R CRAN.

A Bayesian approach to nonlinear inverse problems is considered where the unknown quantity (input) is a random spatial field. The forward model is complex and non-linear, therefore computationally expensive. An emulator-based methodology is developed, where the Bayesian multivariate adaptive regression splines (BMARS) are used to model the function that maps the inputs to the outputs. Discrete cosine transformation (DCT) is used for dimension reduction of the input spatial field. The posterior sampling is carried out using trans-dimensional Markov Chain Monte Carlo (MCMC) methods. Numerical results are presented by analyzing simulated as well as real data on hydrocarbon reservoir characterization.

This paper studies the probabilistic hosting capacity analysis (PHCA) problem in distribution networks considering uncertainties from distributed energy resources (DERs) and residential loads. PHCA aims to compute the hosting capacity, which is defined as the maximal level of DERs that can be securely integrated into a distribution network while satisfying operational constraints with high probability. We formulate PHCA as a chance-constrained optimization problem, and model the uncertainties from DERs and loads using historical data. Due to non-convexities and a substantial number of historical scenarios being used, PHCA is often formulated as large-scale nonlinear optimization problem, thus computationally intractable to solve. To address the core computational challenges, we propose a fast and extensible framework to solve PHCA based on Bayesian Optimization (BayesOpt). Comparing with state-of-the-art algorithms such as interior point and active set, numerical results show that the proposed BayesOpt approach is able to find better solutions (25% higher hosting capacity) with 70% savings in computation time on average.

Gaussian graphical models (GGMs) are well-established tools for probabilistic exploration of dependence structures using precision matrices. We develop a Bayesian method to incorporate covariate information in this GGMs setup in a nonlinear seemingly unrelated regression framework. We propose a joint predictor and graph selection model and develop an efficient collapsed Gibbs sampler algorithm to search the joint model space. Furthermore, we investigate its theoretical variable selection properties. We demonstrate our method on a variety of simulated data, concluding with a real data set from the TCPA project.

Robust Bayesian methods for high-dimensional regression problems under diverse sparse regimes are studied. Traditional shrinkage priors are primarily designed to detect a handful of signals from tens of thousands of predictors in the so-called ultra-sparsity domain. However, they may not perform desirably when the degree of sparsity is moderate. In this paper, we propose a robust sparse estimation method under diverse sparsity regimes, which has a tail-adaptive shrinkage property. In this property, the tail-heaviness of the prior adjusts adaptively, becoming larger or smaller as the sparsity level increases or decreases, respectively, to accommodate more or fewer signals, a posteriori. We propose a global-local-tail (GLT) Gaussian mixture distribution that ensures this property. We examine the role of the tail-index of the prior in relation to the underlying sparsity level and demonstrate that the GLT posterior contracts at the minimax optimal rate for sparse normal mean models. We apply both the GLT prior and the Horseshoe prior to a real data problem and simulation examples. Our findings indicate that the varying tail rule based on the GLT prior offers advantages over a fixed tail rule based on the Horseshoe prior in diverse sparsity regimes., Comment: Accepted in Electronic Journal of Statistics

Currently, novel coronavirus disease 2019 (COVID-19) is a big threat to global health. The rapid spread of the virus has created pandemic, and countries all over the world are struggling with a surge in COVID-19 infected cases. There are no drugs or other therapeutics approved by the US Food and Drug Administration to prevent or treat COVID-19: information on the disease is very limited and scattered even if it exists. This motivates the use of data integration, combining data from diverse sources and eliciting useful information with a unified view of them. In this paper, we propose a Bayesian hierarchical model that integrates global data for real-time prediction of infection trajectory for multiple countries. Because the proposed model takes advantage of borrowing information across multiple countries, it outperforms an existing individual country-based model. As fully Bayesian way has been adopted, the model provides a powerful predictive tool endowed with uncertainty quantification. Additionally, a joint variable selection technique has been integrated into the proposed modeling scheme, which aimed to identify possible country-level risk factors for severe disease due to COVID-19.

In recent biomedical scientific problems, it is a fundamental issue to integratively cluster a set of objects from multiple sources of datasets. Such problems are mostly encountered in genomics, where data is collected from various sources, and typically represent distinct yet complementary information. Integrating these data sources for multi-source clustering is challenging due to their complex dependence structure including directional dependency. Particularly in genomics studies, it is known that there is certain directional dependence between DNA expression, DNA methylation, and RNA expression, widely called The Central Dogma. Most of the existing multi-view clustering methods either assume an independent structure or pair-wise (non-directional) dependency, thereby ignoring the directional relationship. Motivated by this, we propose a copula-based multi-view clustering model where a copula enables the model to accommodate the directional dependence existing in the datasets. We conduct a simulation experiment where the simulated datasets exhibiting inherent directional dependence: it turns out that ignoring the directional dependence negatively affects the clustering performance. As a real application, we applied our model to the breast cancer tumor samples collected from The Cancer Genome Altas (TCGA).

Estimating the marginal and joint densities of the long-term average intakes of different dietary components is an important problem in nutritional epidemiology. Since these variables cannot be directly measured, data are usually collected in the form of 24-hour recalls of the intakes, which show marked patterns of conditional heteroscedasticity. Significantly compounding the challenges, the recalls for episodically consumed dietary components also include exact zeros. The problem of estimating the density of the latent long-time intakes from their observed measurement error contaminated proxies is then a problem of deconvolution of densities with zero-inflated data. We propose a Bayesian semiparametric solution to the problem, building on a novel hierarchical latent variable framework that translates the problem to one involving continuous surrogates only. Crucial to accommodating important aspects of the problem, we then design a copula-based approach to model the involved joint distributions, adopting different modeling strategies for the marginals of the different dietary components. We design efficient Markov chain Monte Carlo algorithms for posterior inference and illustrate the efficacy of the proposed method through simulation experiments. Applied to our motivating nutritional epidemiology problems, compared to other approaches, our method provides more realistic estimates of the consumption patterns of episodically consumed dietary components.

Gaussian graphical models are a popular tool to learn the dependence structure in the form of a graph among variables of interest. Bayesian methods have gained in popularity in the last two decades due to their ability to simultaneously learn the covariance and the graph and characterize uncertainty in the selection. For scalability of the Markov chain Monte Carlo algorithms, decomposability is commonly imposed on the graph space. A wide variety of graphical conjugate priors are proposed jointly on the covariance matrix and the graph with improved algorithms to search along the space of decomposable graphs, rendering the methods extremely popular in the context of multivariate dependence modeling. {\it An open problem} in Bayesian decomposable structure learning is whether the posterior distribution is able to select a meaningful decomposable graph that it is ``close'' in an appropriate sense to the true non-decomposable graph, when the dimension of the variables increases with the sample size. In this article, we explore specific conditions on the true precision matrix and the graph which results in an affirmative answer to this question using a commonly used hyper-inverse Wishart prior on the covariance matrix and a suitable complexity prior on the graph space, both in the well-specified and misspecified settings. In absence of structural sparsity assumptions, our strong selection consistency holds in a high dimensional setting where $p = O(n^{\alpha})$ for $\alpha < 1/3$. We show when the true graph is non-decomposable, the posterior distribution on the graph concentrates on a set of graphs that are {\it minimal triangulations} of the true graph., Comment: 43 pages

Conditional density estimation (density regression) estimates the distribution of a response variable y conditional on covariates x. Utilizing a partition model framework, a conditional density estimation method is proposed using logistic Gaussian processes. The partition is created using a Voronoi tessellation and is learned from the data using a reversible jump Markov chain Monte Carlo algorithm. The Markov chain Monte Carlo algorithm is made possible through a Laplace approximation on the latent variables of the logistic Gaussian process model. This approximation marginalizes the parameters in each partition element, allowing an efficient search of the posterior distribution of the tessellation. The method has desirable consistency properties. In simulation and applications, the model successfully estimates the partition structure and conditional distribution of y.

We develop a Bayesian methodology aimed at simultaneously estimating low-rank and row-sparse matrices in a high-dimensional multiple-response linear regression model. We consider a carefully devised shrinkage prior on the matrix of regression coefficients which obviates the need to specify a prior on the rank, and shrinks the regression matrix towards low-rank and row-sparse structures. We provide theoretical support to the proposed methodology by proving minimax optimality of the posterior mean under the prediction risk in ultra-high dimensional settings where the number of predictors can grow sub-exponentially relative to the sample size. A one-step post-processing scheme induced by group lasso penalties on the rows of the estimated coefficient matrix is proposed for variable selection, with default choices of tuning parameters. We additionally provide an estimate of the rank using a novel optimization function achieving dimension reduction in the covariate space. We exhibit the performance of the proposed methodology in an extensive simulation study and a real data example.

Graphical models are ubiquitous tools to describe the interdependence between variables measured simultaneously such as large-scale gene or protein expression data. Gaussian graphical models (GGMs) are well-established tools for probabilistic exploration of dependence structures using precision matrices and they are generated under a multivariate normal joint distribution. However, they suffer from several shortcomings since they are based on Gaussian distribution assumptions. In this article, we propose a Bayesian quantile based approach for sparse estimation of graphs. We demonstrate that the resulting graph estimation is robust to outliers and applicable under general distributional assumptions. Furthermore, we develop efficient variational Bayes approximations to scale the methods for large data sets. Our methods are applied to a novel cancer proteomics data dataset wherein multiple proteomic antibodies are simultaneously assessed on tumor samples using reverse-phase protein arrays (RPPA) technology.

In this paper, we study porous media flows in heterogeneous stochastic media. We propose an efficient forward simulation technique that is tailored for variational Bayesian inversion. As a starting point, the proposed forward simulation technique decomposes the solution into the sum of separable functions (with respect to randomness and the space), where each term is calculated based on a variational approach. This is similar to Proper Generalized Decomposition (PGD). Next, we apply a multiscale technique to solve for each term and, further, decompose the random function into 1D fields. As a result, our proposed method provides an approximation hierarchy for the solution as we increase the number of terms in the expansion and, also, increase the spatial resolution of each term. We use the hierarchical solution distributions in a variational Bayesian approximation to perform uncertainty quantification in the inverse problem. We conduct a detailed numerical study to explore the performance of the proposed uncertainty quantification technique and show the theoretical posterior concentration.

Significant advances in biotechnology have allowed for simultaneous measurement of molecular data points across multiple genomic and transcriptomic levels from a single tumor/cancer sample. This has motivated systematic approaches to integrate multi-dimensional structured datasets since cancer development and progression is driven by numerous co-ordinated molecular alterations and the interactions between them. We propose a novel two-step Bayesian approach that combines a variable selection framework with integrative structure learning between multiple sources of data. The structure learning in the first step is accomplished through novel joint graphical models for heterogeneous (mixed scale) data allowing for flexible incorporation of prior knowledge. This structure learning subsequently informs the variable selection in the second step to identify groups of molecular features within and across platforms associated with outcomes of cancer progression. The variable selection strategy adjusts for collinearity and multiplicity, and also has theoretical justifications. We evaluate our methods through simulations and apply them to a motivating genomic (DNA copy number and methylation) and transcriptomic (mRNA expression) data for assessing important markers associated with Glioblastoma progression.

We propose an efficient way to sample from a class of structured multivariate Gaussian distributions which routinely arise as conditional posteriors of model parameters that are assigned a conditionally Gaussian prior. The proposed algorithm only requires matrix operations in the form of matrix multiplications and linear system solutions. We exhibit that the computational complexity of the proposed algorithm grows linearly with the dimension unlike existing algorithms relying on Cholesky factorizations with cubic orders of complexity. The algorithm should be broadly applicable in settings where Gaussian scale mixture priors are used on high dimensional model parameters. We provide an illustration through posterior sampling in a high dimensional regression setting with a horseshoe prior on the vector of regression coefficients.