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An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis
Differential abundance analysis is a crucial task in many microbiome studies, where the central goal is to identify microbiome taxa associated with certain biological or clinical conditions. There are two different modes of microbiome differential abundance analysis: the individual-based univariate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491633/ https://www.ncbi.nlm.nih.gov/pubmed/31068967 http://dx.doi.org/10.3389/fgene.2019.00350 |
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author | Banerjee, Kalins Zhao, Ni Srinivasan, Arun Xue, Lingzhou Hicks, Steven D. Middleton, Frank A. Wu, Rongling Zhan, Xiang |
author_facet | Banerjee, Kalins Zhao, Ni Srinivasan, Arun Xue, Lingzhou Hicks, Steven D. Middleton, Frank A. Wu, Rongling Zhan, Xiang |
author_sort | Banerjee, Kalins |
collection | PubMed |
description | Differential abundance analysis is a crucial task in many microbiome studies, where the central goal is to identify microbiome taxa associated with certain biological or clinical conditions. There are two different modes of microbiome differential abundance analysis: the individual-based univariate differential abundance analysis and the group-based multivariate differential abundance analysis. The univariate analysis identifies differentially abundant microbiome taxa subject to multiple correction under certain statistical error measurements such as false discovery rate, which is typically complicated by the high-dimensionality of taxa and complex correlation structure among taxa. The multivariate analysis evaluates the overall shift in the abundance of microbiome composition between two conditions, which provides useful preliminary differential information for the necessity of follow-up validation studies. In this paper, we present a novel Adaptive multivariate two-sample test for Microbiome Differential Analysis (AMDA) to examine whether the composition of a taxa-set are different between two conditions. Our simulation studies and real data applications demonstrated that the AMDA test was often more powerful than several competing methods while preserving the correct type I error rate. A free implementation of our AMDA method in R software is available at https://github.com/xyz5074/AMDA. |
format | Online Article Text |
id | pubmed-6491633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64916332019-05-08 An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis Banerjee, Kalins Zhao, Ni Srinivasan, Arun Xue, Lingzhou Hicks, Steven D. Middleton, Frank A. Wu, Rongling Zhan, Xiang Front Genet Genetics Differential abundance analysis is a crucial task in many microbiome studies, where the central goal is to identify microbiome taxa associated with certain biological or clinical conditions. There are two different modes of microbiome differential abundance analysis: the individual-based univariate differential abundance analysis and the group-based multivariate differential abundance analysis. The univariate analysis identifies differentially abundant microbiome taxa subject to multiple correction under certain statistical error measurements such as false discovery rate, which is typically complicated by the high-dimensionality of taxa and complex correlation structure among taxa. The multivariate analysis evaluates the overall shift in the abundance of microbiome composition between two conditions, which provides useful preliminary differential information for the necessity of follow-up validation studies. In this paper, we present a novel Adaptive multivariate two-sample test for Microbiome Differential Analysis (AMDA) to examine whether the composition of a taxa-set are different between two conditions. Our simulation studies and real data applications demonstrated that the AMDA test was often more powerful than several competing methods while preserving the correct type I error rate. A free implementation of our AMDA method in R software is available at https://github.com/xyz5074/AMDA. Frontiers Media S.A. 2019-04-24 /pmc/articles/PMC6491633/ /pubmed/31068967 http://dx.doi.org/10.3389/fgene.2019.00350 Text en Copyright © 2019 Banerjee, Zhao, Srinivasan, Xue, Hicks, Middleton, Wu and Zhan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Banerjee, Kalins Zhao, Ni Srinivasan, Arun Xue, Lingzhou Hicks, Steven D. Middleton, Frank A. Wu, Rongling Zhan, Xiang An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis |
title | An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis |
title_full | An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis |
title_fullStr | An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis |
title_full_unstemmed | An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis |
title_short | An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis |
title_sort | adaptive multivariate two-sample test with application to microbiome differential abundance analysis |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491633/ https://www.ncbi.nlm.nih.gov/pubmed/31068967 http://dx.doi.org/10.3389/fgene.2019.00350 |
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