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A general framework for association analysis of microbial communities on a taxonomic tree
MOTIVATION: Association analysis of microbiome composition with disease-related outcomes provides invaluable knowledge towards understanding the roles of microbes in the underlying disease mechanisms. Proper analysis of sparse compositional microbiome data is challenging. Existing methods rely on st...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408811/ https://www.ncbi.nlm.nih.gov/pubmed/28003264 http://dx.doi.org/10.1093/bioinformatics/btw804 |
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author | Tang, Zheng-Zheng Chen, Guanhua Alekseyenko, Alexander V Li, Hongzhe |
author_facet | Tang, Zheng-Zheng Chen, Guanhua Alekseyenko, Alexander V Li, Hongzhe |
author_sort | Tang, Zheng-Zheng |
collection | PubMed |
description | MOTIVATION: Association analysis of microbiome composition with disease-related outcomes provides invaluable knowledge towards understanding the roles of microbes in the underlying disease mechanisms. Proper analysis of sparse compositional microbiome data is challenging. Existing methods rely on strong assumptions on the data structure and fail to pinpoint the associated microbial communities. RESULTS: We develop a general framework to: (i) perform robust association tests for the microbial community that exhibits arbitrary inter-taxa dependencies; (ii) localize lineages on the taxonomic tree that are associated with covariates (e.g. disease status); and (iii) assess the overall association of the whole microbial community with the covariates. Unlike existing methods for microbiome association analysis, our framework does not make any distributional assumptions on the microbiome data; it allows for the adjustment of confounding variables and accommodates excessive zero observations; and it incorporates taxonomic information. We perform extensive simulation studies under a wide-range of scenarios to evaluate the new methods and demonstrate substantial power gain over existing methods. The advantages of the proposed framework are further demonstrated with real datasets from two microbiome studies. The relevant R package miLineage is publicly available. AVAILABILITY AND IMPLEMENTATION: miLineage package, manual and tutorial are available at https://medschool.vanderbilt.edu/tang-lab/software/miLineage. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-5408811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54088112017-05-03 A general framework for association analysis of microbial communities on a taxonomic tree Tang, Zheng-Zheng Chen, Guanhua Alekseyenko, Alexander V Li, Hongzhe Bioinformatics Original Papers MOTIVATION: Association analysis of microbiome composition with disease-related outcomes provides invaluable knowledge towards understanding the roles of microbes in the underlying disease mechanisms. Proper analysis of sparse compositional microbiome data is challenging. Existing methods rely on strong assumptions on the data structure and fail to pinpoint the associated microbial communities. RESULTS: We develop a general framework to: (i) perform robust association tests for the microbial community that exhibits arbitrary inter-taxa dependencies; (ii) localize lineages on the taxonomic tree that are associated with covariates (e.g. disease status); and (iii) assess the overall association of the whole microbial community with the covariates. Unlike existing methods for microbiome association analysis, our framework does not make any distributional assumptions on the microbiome data; it allows for the adjustment of confounding variables and accommodates excessive zero observations; and it incorporates taxonomic information. We perform extensive simulation studies under a wide-range of scenarios to evaluate the new methods and demonstrate substantial power gain over existing methods. The advantages of the proposed framework are further demonstrated with real datasets from two microbiome studies. The relevant R package miLineage is publicly available. AVAILABILITY AND IMPLEMENTATION: miLineage package, manual and tutorial are available at https://medschool.vanderbilt.edu/tang-lab/software/miLineage. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-05-01 2016-12-21 /pmc/articles/PMC5408811/ /pubmed/28003264 http://dx.doi.org/10.1093/bioinformatics/btw804 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Papers Tang, Zheng-Zheng Chen, Guanhua Alekseyenko, Alexander V Li, Hongzhe A general framework for association analysis of microbial communities on a taxonomic tree |
title | A general framework for association analysis of microbial communities on a taxonomic tree |
title_full | A general framework for association analysis of microbial communities on a taxonomic tree |
title_fullStr | A general framework for association analysis of microbial communities on a taxonomic tree |
title_full_unstemmed | A general framework for association analysis of microbial communities on a taxonomic tree |
title_short | A general framework for association analysis of microbial communities on a taxonomic tree |
title_sort | general framework for association analysis of microbial communities on a taxonomic tree |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408811/ https://www.ncbi.nlm.nih.gov/pubmed/28003264 http://dx.doi.org/10.1093/bioinformatics/btw804 |
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