Evidence map›Paper›PMID 28178947›Full record

ArticleBMC bioinformatics2017

An integrative Bayesian Dirichlet-multinomial regression model for the analysis of taxonomic abundances in microbiome data.

W Duncan Wadsworth, Raffaele Argiento, Michele Guindani, Jessica Galloway-Pena, Samuel A Shelburne, Marina Vannucci

Erratum issuedAbstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

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  5. Review
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  12. Analysis of Microbiome Data.Annual review of statistics and its application · 2024
    Article
  13. Article
  14. Cultural transmission of move choice in chess.Proceedings. Biological sciences · 2023
    Article
  15. Article
  16. sccomp: Robust differential composition and variability analysis for single-cell data.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Sparse tree-based clustering of microbiome data to characterize microbiome heterogeneity in pancreatic cancer.Journal of the Royal Statistical Society. Series C, Applied statistics · 2023
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

W Duncan WadsworthDepartment of Statistics, Rice University, Houston, TX, USA.
Raffaele ArgientoESOMAS Department, University of Torino and Collegio Carlo Alberto, Torino, Italy.
Michele GuindaniDepartment of Statistics, University of California, Irvine, CA, USA.
Jessica Galloway-PenaDepartment of Infectious Disease, Infection Control, and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA.
Samuel A ShelburneDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA.
Marina VannucciDepartment of Statistics, Rice University, Houston, TX, USA. marina@rice.edu.ORCID 0000-0002-7360-5321

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Training Program in Biostatistics for Cancer ResearchT32CA096520 · NCI · RICE UNIVERSITY · PI KIMMEL, MAREK, YUAN, YING · 2003 to 2023
$4.5M
NCI NIH HHS L30 CA209245NCI NIH HHS P30 CA016672NCI NIH HHS T32 CA096520
6 · The paper itself

Abstract

backgroundThe Human Microbiome has been variously associated with the immune-regulatory mechanisms involved in the prevention or development of many non-infectious human diseases such as autoimmunity, allergy and cancer. Integrative approaches which aim at associating the composition of the human microbiome with other available information, such as clinical covariates and environmental predictors, are paramount to develop a more complete understanding of the role of microbiome in disease development.

resultsIn this manuscript, we propose a Bayesian Dirichlet-Multinomial regression model which uses spike-and-slab priors for the selection of significant associations between a set of available covariates and taxa from a microbiome abundance table. The approach allows straightforward incorporation of the covariates through a log-linear regression parametrization of the parameters of the Dirichlet-Multinomial likelihood. Inference is conducted through a Markov Chain Monte Carlo algorithm, and selection of the significant covariates is based upon the assessment of posterior probabilities of inclusions and the thresholding of the Bayesian false discovery rate. We design a simulation study to evaluate the performance of the proposed method, and then apply our model on a publicly available dataset obtained from the Human Microbiome Project which associates taxa abundances with KEGG orthology pathways. The method is implemented in specifically developed R code, which has been made publicly available.

conclusionsOur method compares favorably in simulations to several recently proposed approaches for similarly structured data, in terms of increased accuracy and reduced false positive as well as false negative rates. In the application to the data from the Human Microbiome Project, a close evaluation of the biological significance of our findings confirms existing associations in the literature.

Indexed as

Linear ModelsMicrobiotaAlgorithmsBacteriaBayes TheoremComputer SimulationHumansMarkov ChainsMonte Carlo MethodBayesian hierarchical modelData integrationDirichlet-multinomialMicrobiome dataVariable selection

Identifiers

PMID28178947
PMCPMC5299727

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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.