Evidence map›Paper›PMID 39853798›Full record

ArticleStatistics in medicine2025

A Generalized Bayesian Stochastic Block Model for Microbiome Community Detection.

Kevin C Lutz, Michael L Neugent, Tejasv Bedi, Nicole J De Nisco, Qiwei Li

Abstract read
In one paragraph

Article in Statistics in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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. Article
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.

Kevin C LutzPeter O'Donnell Jr. School of Public Health, The University of Texas Southwestern Medical Center, Dallas, Texas.ORCID 0000-0002-6687-0637
Michael L NeugentDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, Texas.ORCID 0000-0002-9863-9595
Tejasv BediDepartment of Mathematical Sciences, The University of Texas at Dallas, Richardson, Texas.ORCID 0000-0001-7532-4075
Nicole J De NiscoDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, Texas.ORCID 0000-0002-7670-5301
Qiwei LiDepartment of Mathematical Sciences, The University of Texas at Dallas, Richardson, Texas.ORCID 0000-0002-1020-3050

Funding

Defining the dynamics of urobiome structure and function in postmenopausal women and its role in recurrent UTI susceptibilityR01DK131267 · NIDDK · UNIVERSITY OF TEXAS DALLAS · PI DE NISCO, NICOLE JANELL · 2021 to 2025
$1.5M
Developing novel algorithms for spatial molecular profiling technologiesR01GM141519 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI XIAO, GUANGHUA · 2021 to 2024
$1.4M
Mechanistic basis of urinary Lactobacillus enrichment by estrogen hormone therapyF32DK128975 · NIDDK · UNIVERSITY OF TEXAS DALLAS · PI NEUGENT, MICHAEL LEE · 2022 to 2024
$218k
National Science Foundation 2113674National Science Foundation 2210912NIDDK NIH HHS F32 DK128975NIDDK NIH HHS R01 DK131267NIGMS NIH HHS R01 GM141519NIH HHS 1F32DK128975-01A1NIH HHS 1R01DK131267-01NIH HHS 1R01GM141519Welch Foundation AT-2030-20200401
6 · The paper itself

Abstract

Advances in next-generation sequencing technology have enabled the high-throughput profiling of metagenomes and accelerated microbiome studies. Recently, there has been a rise in quantitative studies that aim to decipher the microbiome co-occurrence network and its underlying community structure based on metagenomic sequence data. Uncovering the complex microbiome community structure is essential to understanding the role of the microbiome in disease progression and susceptibility. Taxonomic abundance data generated from metagenomic sequencing technologies are high-dimensional and compositional, suffering from uneven sampling depth, over-dispersion, and zero-inflation. These characteristics often challenge the reliability of the current methods for microbiome community detection. To study the microbiome co-occurrence network and perform community detection, we propose a generalized Bayesian stochastic block model that is tailored for microbiome data analysis where the data are transformed using the recently developed modified centered-log ratio transformation. Our model also allows us to leverage taxonomic tree information using a Markov random field prior. The model parameters are jointly inferred by using Markov chain Monte Carlo sampling techniques. Our simulation study showed that the proposed approach performs better than competing methods even when taxonomic tree information is non-informative. We applied our approach to a real urinary microbiome dataset from postmenopausal women. To the best of our knowledge, this is the first time the urinary microbiome co-occurrence network structure in postmenopausal women has been studied. In summary, this statistical methodology provides a new tool for facilitating advanced microbiome studies.

Indexed as

MicrobiotaModels, StatisticalBayes TheoremComputer SimulationFemaleHigh-Throughput Nucleotide SequencingHumansMarkov ChainsMetagenomicsMonte Carlo MethodPostmenopauseStochastic ProcessesBayesian stochastic block modelcommunity detectionMarkov random fieldmicrobiome co‐occurrence networktaxonomic tree

Identifiers

PMID39853798
PMCPMC11760646

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.