Dynamic ICAR Spatiotemporal Factor Models

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Hwasoo Shin, Marco A.R. Ferreira
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Abstract

We propose a novel class of dynamic factor models for spatiotemporal areal data. This novel class of models assumes that the spatiotemporal process may be represented by some few latent factors that evolve through time according to dynamic linear models. As the dimension of the vector of latent factors is typically much smaller than the number of subregions, our proposed class of models may achieve substantial dimension reduction. At each time point, the vector of observations is linearly related to the vector of latent factors through a matrix of factor loadings. Each column of this matrix may be seen as a vectorized map of factor loadings relating one latent factor to the vector of observations. Thus, to account for spatial dependence, we assume that each column of the matrix of factor loadings follows an intrinsic conditional autoregressive (ICAR) process. Hence, we call our class of models the Dynamic ICAR Spatiotemporal Factor Models (DIFM). We develop a Gibbs sampler for exploration of the posterior distribution. In addition, we develop model selection through a Laplace-Metropolis estimator of the predictive density. We present two case studies. The first case study, which is for simulated data, demonstrates that our DIFMs are identifiable and that our proposed inferential procedure works well at recovering the underlying data generating process. Finally, the second case study demonstrates the utility and flexibility of our DIFM framework with an application to the drug overdose epidemic in the United States from 2015 to 2021.

动态ICAR时空因子模型
我们提出了一类新的时空面数据动态因子模型。这类新模型假设时空过程可以由一些随时间演变的潜在因素来表示,这些潜在因素是根据动态线性模型来表示的。由于潜在因素向量的维数通常比子区域的数量小得多,因此我们提出的这类模型可以实现大幅度的降维。在每个时间点,观测向量通过因子负荷矩阵与潜在因子向量线性相关。该矩阵的每一列可以看作是一个潜在因素与观测向量相关的因素负荷的矢量化图。因此,为了考虑空间依赖性,我们假设因子负荷矩阵的每一列都遵循一个内在条件自回归(ICAR)过程。因此,我们将这类模型称为动态ICAR时空因子模型(DIFM)。我们开发了吉布斯采样器来探索后验分布。此外,我们通过预测密度的Laplace-Metropolis估计器开发了模型选择。我们提出两个案例研究。第一个案例研究是针对模拟数据的,它证明了我们的difm是可识别的,并且我们提出的推理过程在恢复底层数据生成过程方面工作得很好。最后,第二个案例研究展示了我们的DIFM框架的实用性和灵活性,并将其应用于美国2015年至2021年的药物过量流行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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