Evidence map›Paper›PMID 34714989›Full record

ArticleStatistical applications in genetics and molecular biology2021

A hierarchical Bayesian approach for detecting global microbiome associations.

Farhad Hatami, Emma Beamish, Albert Davies, Rachael Rigby, Frank Dondelinger

Abstract read
In one paragraph

Article in Statistical applications in genetics and molecular biology, 2021. 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
0cells of the map it votes in
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.

Farhad HatamiCentre for Health Informatics Computation and Statistics, Lancaster University, Lancaster, UK.
Emma BeamishDepartment of Musculoskeletal Biology, University of Liverpool, Liverpool, UK.
Albert DaviesFurness General Hospital, Barrow-In-Furness, UK.
Rachael RigbyDepartment of Biomedicine and Life Sciences, Lancaster University, Lancaster, UK.
Frank DondelingerCentre for Health Informatics Computation and Statistics, Lancaster University, Lancaster, UK.ORCID 0000-0003-1816-6300

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human gut microbiome has been shown to be associated with a variety of human diseases, including cancer, metabolic conditions and inflammatory bowel disease. Current approaches for detecting microbiome associations are limited by relying on specific measures of ecological distance, or only allowing for the detection of associations with individual bacterial species, rather than the whole microbiome. In this work, we develop a novel hierarchical Bayesian model for detecting global microbiome associations. Our method is not dependent on a choice of distance measure, and is able to incorporate phylogenetic information about microbial species. We perform extensive simulation studies and show that our method allows for consistent estimation of global microbiome effects. Additionally, we investigate the performance of the model on two real-world microbiome studies: a study of microbiome-metabolome associations in inflammatory bowel disease, and a study of associations between diet and the gut microbiome in mice. We show that we can use the method to reliably detect associations in real-world datasets with varying numbers of samples and covariates.

Indexed as

Gastrointestinal MicrobiomeInflammatory Bowel DiseasesMicrobiotaAnimalsBayes TheoremMicePhylogenyBayesian modelingglobal effectsmicrobiome

Identifiers

PMID34714989
PMCPMC9125803

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.