Scalable Calibration of Individual-Based Epidemic Models through Categorical Approximations
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Traditional compartmental models capture population-level dynamics but fail to characterize individual-level risk. The computational cost of exact likelihood evaluation for partially observed individual-based models, however, grows exponentially with the population size, necessitating approximate inference. Existing sampling-based methods usually require multiple simulations of the individuals in the population and rely on bespoke proposal distributions or summary statistics. We propose a deterministic approach to approximating the likelihood using categorical distributions. The approximate likelihood is amenable to automatic differentiation so that parameters can be estimated by maximization or posterior sampling using standard software libraries such as TensorFlow with little user effort. We prove the consistency of the maximum approximate likelihood estimator. We empirically test our approach on several classes of individual-based models for epidemiology: different sets of disease states, individual-specific transition rates, spatial interactions, under-reporting and misreporting. We demonstrate ground truth recovery and comparable log-likelihood values at substantially reduced cost compared to competitor methods. Finally, we show the scalability and effectiveness of our approach with a real-world application on the 2001 UK Foot-and-Mouth outbreak, where the simplicity of the CAL allows us to include 162775 farms.
RBF 核高斯过程最大似然估计的精确渐近理论
Gaussian processes (GPs) are widely used across machine learning, spatial statistics, time-series analysis, optimization, Bayesian statistics, and scientific applications. A central component of a GP model is its kernel, which is typically specified through a parametric family. Among the most widely used choices is the radial basis function (RBF), also known as the squared exponential or Gaussian kernel, owing to its simple form, smoothness, and flexibility. In practice, the…
面向高维数据的残差树高斯过程建模框架
With the advance of measurement technologies and increasing computing power, large spatial data with heterogeneous structures are often collected over high-dimensional domains. Existing Gaussian process (GP) models and computational strategies are often inadequate for analyzing such datasets in multi-dimensional domains. To address these challenges, we develop a Bayesian residual tree GP methodology called ResTGP for large spatial data with potentially heterogeneous…
基于预测生成树方法的贝叶斯空间区域划分一致估计
Bayesian model-based spatial clustering methods are widely used for their flexibility in estimating latent clusters with an unknown number of clusters while accounting for spatial proximity. Many existing methods are designed for clustering finite spatial units, limiting their ability to make predictions or may impose restrictive geometric constraints on the shapes of subregions. Furthermore, the posterior clustering consistency theory of spatial clustering models remains…
贝叶斯神经网络辅助多处理混合治愈生存模型:儿科肿瘤应用
Estimating covariate-conditional treatment effects in multi-arm oncology studies is complicated when treatment arms have common distributional features and a non-negligible fraction of patients achieve long-term remission. We propose a joint mixture cure model with covariate-dependent mixtures of log-normal kernels with treatment-specific inclusions. Both linear and neural-network-assisted non-linear covariate links are proposed. Specifically, the susceptible survival…
图分割贝叶斯因果森林:空间异质性处理效应估计
In spatial observational studies, treatment assignment and outcomes often exhibit spatial dependence patterns, and treatment effects may vary across space and subpopulations due to both measured and unmeasured spatially structured confounders. Accounting for spatial dependence while estimating heterogeneous treatment effects (HTEs) is a central task in spatial causal inference. Causal Bayesian additive regression tree methods are popular nonparametric methods for modeling…
检测异质组织跨样本空间表达变异的灵活贝叶斯框架
Spatial transcriptomics measures gene expression alongside the spatial coordinates of each capture spot or cell across tissue samples. The detection of spatially variable (SV) genes, whose expression exhibits systematic spatial variation, enables the delineation of functional tissue domains and the identification of region-specific transcriptional changes that underlie disease heterogeneity. However, empirical evidence from spatial transcriptomics data indicates that…