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Tytuł pozycji:

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

Tytuł:
MegaR: an interactive R package for rapid sample classification and phenotype prediction using metagenome profiles and machine learning.
Autorzy:
Dhungel E; Program in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Mreyoud Y; Program in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Gwak HJ; Department of Computer Science and Engineering, Hanyang University, Seoul, Korea.
Rajeh A; Program in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Rho M; Department of Computer Science and Engineering, Hanyang University, Seoul, Korea.
Ahn TH; Program in Bioinformatics and Computational Biology, Saint Louis University, Saint Louis, MO, USA. .; Department of Computer Science, Saint Louis University, Saint Louis, MO, USA. .
Źródło:
BMC bioinformatics [BMC Bioinformatics] 2021 Jan 18; Vol. 22 (1), pp. 25. Date of Electronic Publication: 2021 Jan 18.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: [London] : BioMed Central, 2000-
MeSH Terms:
Machine Learning*
Metagenome*
Metagenomics*
Humans ; Phenotype ; RNA, Ribosomal, 16S/genetics
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Grant Information:
1564894 National Science Foundation
Contributed Indexing:
Keywords: Machine learning; Metagenomics; Phenotype prediction; R-package; Sample classification
Substance Nomenclature:
0 (RNA, Ribosomal, 16S)
Entry Date(s):
Date Created: 20210119 Date Completed: 20210204 Latest Revision: 20230919
Update Code:
20240105
PubMed Central ID:
PMC7814621
DOI:
10.1186/s12859-020-03933-4
PMID:
33461494
Czasopismo naukowe
Background: Diverse 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.
Results: We 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.
Conclusions: Metagenomic 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.
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