Evidence map›Paper›PMID 42837381›Full record

ArticlePloS one2026

Modeling spatially dependent count time series data using COM-poisson INGARCH Models.

Stephanie Colwell, Prabhakar Chalise, Byron Gajewski, Isuru Panduka Ratnayake, Dinesh Pal Mudaranthakam

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Stephanie ColwellDepartment of Biostatistics & Data Science, University of Kansas Medical Center, Kansas City, Kansas, United States of America.ORCID https://orcid.org/0009-0006-6389-7283
Prabhakar ChaliseDepartment of Biostatistics & Data Science, University of Kansas Medical Center, Kansas City, Kansas, United States of America.
Byron GajewskiDepartment of Biostatistics & Data Science, University of Kansas Medical Center, Kansas City, Kansas, United States of America.
Isuru Panduka RatnayakeDepartment of Biostatistics & Data Science, University of Kansas Medical Center, Kansas City, Kansas, United States of America.ORCID https://orcid.org/0000-0001-9596-781X
Dinesh Pal MudaranthakamDepartment of Biostatistics & Data Science, University of Kansas Medical Center, Kansas City, Kansas, United States of America.

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
NCI NIH HHS P30 CA168524NIGMS NIH HHS P20 GM103418
6 · The paper itself

Abstract

Count time series frequently exhibit serial dependence and either overdispersion or underdispersion relative to the Poisson equidispersion assumption. When such counts are observed across multiple locations, spatial dependence often arises, resulting in complex spatio-temporal dependency structures that are not adequately accommodated by standard integer-valued generalized autoregressive conditional heteroskedasticity (INGARCH) models. To address these challenges, this study proposes a spatial Conway-Maxwell-Poisson INGARCH (SP-COM-INGARCH) framework that jointly models temporal dependence, spatial interaction, and varying dispersion. The proposed framework incorporates the Conway-Maxwell-Poisson (COM-Poisson) distribution, which accommodates both overdispersion and underdispersion through an additional dispersion parameter, while a spatially weighted lag structure captures dependence across neighboring locations. We further introduce covariate-adjusted identity-link and softplus-link extensions. In particular, the softplus formulation allows covariates to have negative effects while ensuring positivity of the conditional COM-Poisson centering parameter. For the SP-COM-INGARCH (1,1) process sufficient conditions for stationarity and ergodicity are established, and expressions for the conditional first- and second-order moments are derived. The finite-sample performance of conditional maximum likelihood estimation is evaluated through simulations under several overdispersion and underdispersion scenarios. Parameter recovery is generally satisfactory, with accuracy tending to improve as the length of the time-series increases. We illustrate the framework using weekly influenza-like illness counts from Arkansas, Kansas, Missouri, and Oklahoma with absolute humidity as a time-varying covariate. Across six competing COM-Poisson and generalized Poisson models, the softplus SP-COM-INGARCHX model achieved the lowest joint out-of-sample RMSE, while the baseline SP-COM-INGARCH model achieved the lowest joint out-of-sample MAE, although the differences among several models were small. Overall, the proposed SP-COM-INGARCH framework offers a flexible extension for modeling spatiotemporal count data with covariate effects and flexible dispersion while providing competitive out-of-sample forecasting performance.

Indexed as

Models, StatisticalAlgorithmsComputer SimulationPoisson Distribution

Identifiers

PMID42837381
PMCPMC13641397

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.