Evidence map›Paper›PMID 33461494›Full record

ArticleBMC bioinformatics2021

MegaR: an interactive R package for rapid sample classification and phenotype prediction using metagenome profiles and machine learning.

Eliza Dhungel, Yassin Mreyoud, Ho-Jin Gwak, Ahmad Rajeh, Mina Rho, Tae-Hyuk Ahn

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 37% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Frontiers in bioinformatics · 2026
    Article
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  4. Review
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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

6 authors at 3 institutions in 3 countries.

Eliza Dhungel *Program in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Yassin Mreyoud *Program in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Ho-Jin GwakDepartment of Computer Science and Engineering, Hanyang University, Seoul, Korea.
Ahmad RajehProgram in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Mina RhoDepartment of Computer Science and Engineering, Hanyang University, Seoul, Korea.
Tae-Hyuk AhnProgram in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA. taehyuk.ahn@slu.edu.ORCID http://orcid.org/0000-0002-7281-9459
Saint Louis University · USHanyang University · KRSaint Louis University · ES

Funding

National Science Foundation 1564894
6 · The paper itself

Abstract

backgroundDiverse microbiome communities drive biogeochemical processes and evolution of animals in their ecosystems. Many microbiome projects have demonstrated the power of using metagenomics to understand the structures and factors influencing the function of the microbiomes in their environments. In order to characterize the effects from microbiome composition for human health, diseases, and even ecosystems, one must first understand the relationship of microbes and their environment in different samples. Running machine learning model with metagenomic sequencing data is encouraged for this purpose, but it is not an easy task to make an appropriate machine learning model for all diverse metagenomic datasets.

resultsWe introduce MegaR, an R Shiny package and web application, to build an unbiased machine learning model effortlessly with interactive visual analysis. The MegaR employs taxonomic profiles from either whole metagenome sequencing or 16S rRNA sequencing data to develop machine learning models and classify the samples into two or more categories. It provides various options for model fine tuning throughout the analysis pipeline such as data processing, multiple machine learning techniques, model validation, and unknown sample prediction that can be used to achieve the highest prediction accuracy possible for any given dataset while still maintaining a user-friendly experience.

conclusionsMetagenomic sample classification and phenotype prediction is important particularly when it applies to a diagnostic method for identifying and predicting microbe-related human diseases. MegaR provides various interactive visualizations for user to build an accurate machine-learning model without difficulty. Unknown sample prediction with a properly trained model using MegaR will enhance researchers to identify the sample property in a fast turnaround time.

Indexed as

Machine LearningMetagenomeMetagenomicsHumansPhenotypeRNA, Ribosomal, 16SRNA, Ribosomal, 16SMachine learningMetagenomicsPhenotype predictionR-packageSample classification

Identifiers

PMID33461494
PMCPMC7814621
OpenAlexW3123225556

What OpenQuestion 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 OpenQuestion graph.