Evidence map›Paper›PMID 42613133›Full record

ArticleBiostatistics (Oxford, England)2026

A Bayesian multivariate spatial point pattern model: application to oral microbiome FISH image data.

Kyu Ha Lee, Brent A Coull, Suman Majumder, Patrick J La Riviere, Jessica L Mark Welch, Jacqueline R Starr

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Kyu Ha LeeDepartment of Nutrition, Harvard T.H. Chan School of Public Health, 677 Huntington Avenue, Boston, MA 02115, United States.ORCID 0000-0002-5313-8375
Brent A CoullDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, 677 Huntington Avenue, Boston, MA 02115, United States.ORCID 0000-0002-1808-4156
Suman MajumderInterdisciplinary Statistical Research Unit, Indian Statistical Institute, 203 Barrackpore Trunk Road, Kolkata-700108, India.ORCID 0000-0002-3678-5642
Patrick J La RiviereDepartment of Radiology, University of Chicago, 5841 South Maryland Avenue, MC2026, Chicago, IL 60637, United States.
Jessica L Mark WelchDepartment of Microbiology, American Dental Association Forsyth Institute, 100 Chestnut Street, Somerville, MA 02143, United States.
Jacqueline R StarrChanning Division of Network Medicine, Brigham and Women's Hospital, 399 Revolution Drive, Somerville, MA 02145, United States.

Funding

Bayesian multivariate 3D spatial modeling for microbiome image analysisR01GM126257 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, KYU HA, STARR, JACQUELINE R · 2021 to 2024
$2.4M
Bayesian multivariate image analysis for studying oral microbiome biogeographyR21DE026872 · NIDCR · HARVARD SCHOOL OF PUBLIC HEALTH · PI LEE, KYU HA, STARR, JACQUELINE R · 2018 to 2019
$592k
NIDCR NIH HHS R21 DE026872NIDCR NIH HHS R21DE026872NIGMS NIH HHS R01 GM126257NIGMS NIH HHS R01GM126257
6 · The paper itself

Abstract

Advances in cellular imaging technologies, especially those based on fluorescence in situ hybridization (FISH), now allow detailed visualization of the spatial organization of human or bacterial cells. Quantifying this spatial organization is crucial for understanding the function of multicellular tissues or biofilms, with implications for human health and disease. To address the need for better methods to achieve such quantification, we propose a flexible multivariate point process model that characterizes and estimates complex spatial interactions among multiple cell types. The proposed Bayesian framework is appealing due to its unified estimation process and the ability to directly quantify uncertainty in key estimates of interest, such as those of inter-type correlation and the proportion of variance due to inter-type relationships. To ensure stable and interpretable estimation, we consider shrinkage priors for coefficients associated with latent processes that induce dependencies among point patterns. Model selection and comparison are conducted using a deviance information criterion designed for models with latent variables, providing a practical criterion for balancing model fit and complexity. Furthermore, we use a Bayesian hierarchical pooling model to synthesize image-specific posterior summaries, allowing inference at both the global- (across subjects) and subject-specific levels. An R package, mspatPPM, implements an efficient computational scheme based on Hamiltonian Monte Carlo and adaptive Metropolis-Hastings algorithms. Numerical studies evaluate the practical performance of the proposed framework for model selection and for estimating quantities that characterize the multivariate spatial distribution of cell types. We apply the proposed method to microbial biofilm image data from the human tongue dorsum and find that specific taxon pairs, such as Streptococcus mitis-Streptococcus salivarius and S. mitis-Veillonella, exhibit strong positive spatial correlations, while others, such as Actinomyces-Rothia, show slight negative correlations. For most of the taxa, a substantial portion of spatial variance can be attributed to inter-taxon relationships.

Indexed as

Image Processing, Computer-AssistedIn Situ Hybridization, FluorescenceMicrobiotaModels, StatisticalMouthBayes TheoremBiofilmsHumansbiofilmsimage analysislog-Gaussian Cox processMarkov chain Monte Carlospatial point processes

Identifiers

PMID42613133
PMCPMC13485354

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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.