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Jin Hyung Lee

Publications and source records attributed to Jin Hyung Lee.

3 recordsLinked to original sources

A Scalable Variational Bayes Approach for Fitting Non-Conjugate Spatial Generalized Linear Mixed Models via Basis Expansions

Large spatial datasets with non-Gaussian responses are increasingly common in environmental monitoring, ecology, and remote sensing, yet scalable Bayesian inference for such data remains challenging. Markov chain Monte Carlo methods are often prohibitive for large datasets, and existing variational Bayes methods rely on conjugacy or strong approximations that limit their applicability and can underestimate posterior variances. A scalable variational framework that incorporates semi-implicit variational inference (SIVI) with basis representations of spatial generalized linear mixed models, which may not have conjugacy, is proposed. The proposed framework accommodates gamma, negative binomial, Poisson, Bernoulli, and Gaussian responses on continuous spatial domains. Across 20 simulation scenarios with 50,000 locations, SIVI achieves predictive accuracy and posterior distributions comparable to Metropolis--Hastings and Hamiltonian Monte Carlo while providing notable computational speedups. Applications to remotely-sensed land surface temperature and blue jay abundance further demonstrate the utility of the approach for large non-Gaussian spatial datasets.

stat.ME↗

A Scalable Variational Bayes Approach to Fit High-dimensional Spatial Generalized Linear Mixed Models

Gaussian and discrete non-Gaussian spatial datasets are common across fields like public health, ecology, geosciences, and social sciences. Bayesian spatial generalized linear mixed models (SGLMMs) are a flexible class of models for analyzing such data, but they struggle to scale to large datasets. Many scalable Bayesian methods, built upon basis representations or sparse covariance matrices, still rely on posterior sampling via Markov chain Monte Carlo (MCMC). Variational Bayes (VB) methods have been applied to SGLMMs, but only for small areal datasets. We propose two computationally efficient VB approaches for analyzing moderately sized and massive (millions of locations) Gaussian and discrete non-Gaussian spatial data in the continuous spatial domain. Our methods leverage semi-parametric approximations of latent spatial processes and parallel computing to ensure computational efficiency. The proposed methods deliver inferential and predictive performance comparable to gold-standard MCMC methods while achieving computational speedups of up to 3600 times. In most cases, our VB approaches outperform state-of-the-art alternatives such as INLA and Hamiltonian Monte Carlo. We validate our methods through a comparative numerical study and applications to real-world datasets. These VB approaches can enable practitioners to model millions of discrete non-Gaussian spatial observations on standard laptops, significantly expanding access to advanced spatial modeling tools.

stat.ME↗

Deep Learning Super-Resolution Enables Rapid Simultaneous Morphological and Quantitative Magnetic Resonance Imaging

Obtaining magnetic resonance images (MRI) with high resolution and generating quantitative image-based biomarkers for assessing tissue biochemistry is crucial in clinical and research applications. How- ever, acquiring quantitative biomarkers requires high signal-to-noise ratio (SNR), which is at odds with high-resolution in MRI, especially in a single rapid sequence. In this paper, we demonstrate how super-resolution can be utilized to maintain adequate SNR for accurate quantification of the T2 relaxation time biomarker, while simultaneously generating high- resolution images. We compare the efficacy of resolution enhancement using metrics such as peak SNR and structural similarity. We assess accuracy of cartilage T2 relaxation times by comparing against a standard reference method. Our evaluation suggests that SR can successfully maintain high-resolution and generate accurate biomarkers for accelerating MRI scans and enhancing the value of clinical and research MRI.

cs.CV↗