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Guangquan Li

Publications and source records attributed to Guangquan Li.

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A spatio-temporal block aggregation model for latent log Gaussian outcomes: application on modelling wastewater virus concentration in Wales

Wastewater-based epidemiology has emerged as a valuable tool for monitoring community-level infectious disease dynamics, providing population-wide signals that complement clinical surveillance. However, wastewater measurements are often observed as aggregated values over irregular spatial units. This work develops an approach to link an underlying spatially continuous processes and an aggregated outcome. We propose a spatio-temporal model for latent log-Gaussian outcomes that provides a coherent framework for inference and prediction, allowing the process to be integrated over arbitrary spatial configurations. This framework can also be used for subsequent analyses, such as linking wastewater signal to health outcomes at administrative areas. We use a Bayesian framework for inference via the linearised integrated nested Laplace approximation (INLA) approach. We apply the proposed methodology to model SARS-CoV-2 N1 gene copies in wastewater across 47 catchment areas in Wales from the beginning of August 2022 to the end of July 2023. The results demonstrate that the model captures spatial and temporal patterns and has good predictive performance. Results also show that estimated viral gene copies are strongly linked to positivity rates from COVID-19 PCR tests at the local authority level. Our findings highlight the importance of explicitly modelling block aggregation when analysing wastewater surveillance data. The proposed framework provides a flexible and principled approach for integrating environmental surveillance data into public health monitoring systems.

stat.AP

Spatially continuous modelling of aggregated outcome data

This work develops a block aggregation approach to spatial estimation and prediction when the response is observed at a coarse spatial scale, for example as counts of events in administrative areas, or blocks, while covariates are available at a finer spatial resolution, typically as raster images. Our approach specifies a linear predictor at the finer resolution as a combination of covariate effects and a latent, spatially continuous Gaussian process. This linear predictor then determines the distribution of the response through an inverse link function and spatial integration. We use a simulation study to evaluate the performance of the proposed approach in comparison to two industry standard approaches: a traditional geostatistical model that associates each response with the centroid of its block; and a Markov random field (MRF) approach that aggregates covariate data to block-level. As expected, the differences in performance among the three approaches are small with respect to block-level prediction. The rationale for, and advantage of, the block aggregation approach lies in its delivery of reliable inferences at whatever spatial resolution is required in a particular application. We describe two applications: a linear Gaussian sampling model of wastewater virus concentrations in England, using population density as covariate; and log-linear Poisson model of cardiovascular hospitalisations in England using socio-demographic variables at fine-scale administrative units as covariates.

stat.ME

Parameter identifiability and redundancy: theoretical considerations

In this paper we outline general considerations on parameter identifiability, and introduce the notion of weak local identifiability and gradient weak local identifiability. These are based on local properties of the likelihood, in particular the rank of the Hessian matrix. We relate these to the notions of parameter identifiability and redundancy previously introduced by Rothenberg (Econometrica 39 (1971) 577-591) and Catchpole and Morgan (Biometrika 84 (1997) 187-196). Within the exponential family parameter irredundancy, local identifiability, gradient weak local identifiability and weak local identifiability are shown to be equivalent. We consider applications to a recently developed class of cancer models of Little and Wright (Math Biosciences 183 (2003) 111-134) and Little et al. (J Theoret Biol 254 (2008) 229-238) that generalize a large number of other recently used quasi-biological cancer models, in particular those of Armitage and Doll (Br J Cancer 8 (1954) 1-12) and the two-mutation model (Moolgavkar and Venzon Math Biosciences 47 (1979) 55-77).

math.ST