Evidence map›Paper›PMID 34525957›Full record

ArticleBMC genomics2021

Microbial trend analysis for common dynamic trend, group comparison, and classification in longitudinal microbiome study.

Chan Wang, Jiyuan Hu, Martin J Blaser, Huilin Li

Abstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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  3. Review
  4. 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

4 authors.

Chan WangDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, 10016, NY, USA.
Jiyuan HuDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, 10016, NY, USA.
Martin J BlaserCenter for Advanced Biotechnology and Medicine, Rutgers University, Piscataway, 08854-8021, NJ, USA.
Huilin LiDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, 10016, NY, USA. Huilin.Li@nyulangone.org.ORCID http://orcid.org/0000-0002-8288-7068

Funding

Project 2P20CA252728 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG · 2020 to 2022
$3.4M
Novel Statistical Methods in Analyzing Microbiome Data for Longitudinal StudyR01DK110014 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LI, HUILIN · 2016 to 2019
$1.5M
foundation for the national institutes of health 1P20CA252728foundation for the national institutes of health R01DK110014foundation for the national institutes of health U01AI22285NCI NIH HHS P20 CA252728NIDDK NIH HHS R01 DK110014
6 · The paper itself

Abstract

backgroundThe human microbiome is inherently dynamic and its dynamic nature plays a critical role in maintaining health and driving disease. With an increasing number of longitudinal microbiome studies, scientists are eager to learn the comprehensive characterization of microbial dynamics and their implications to the health and disease-related phenotypes. However, due to the challenging structure of longitudinal microbiome data, few analytic methods are available to characterize the microbial dynamics over time.

resultsWe propose a microbial trend analysis (MTA) framework for the high-dimensional and phylogenetically-based longitudinal microbiome data. In particular, MTA can perform three tasks: 1) capture the common microbial dynamic trends for a group of subjects at the community level and identify the dominant taxa; 2) examine whether or not the microbial overall dynamic trends are significantly different between groups; 3) classify an individual subject based on its longitudinal microbial profiling. Our extensive simulations demonstrate that the proposed MTA framework is robust and powerful in hypothesis testing, taxon identification, and subject classification. Our real data analyses further illustrate the utility of MTA through a longitudinal study in mice.

conclusionsThe proposed MTA framework is an attractive and effective tool in investigating dynamic microbial pattern from longitudinal microbiome studies.

Indexed as

Computational BiologyMicrobiotaAnimalsLongitudinal StudiesMiceClassificationCompositionDynamicHigh dimensionalityHypothesis testingLongitudinal microbiomePhylogenetic treeVariable selection

Identifiers

PMID34525957
PMCPMC8442444

What OpenQuestion holds

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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.