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Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing

MOTIVATION: The number of microbial and metagenomic studies has increased drastically due to advancements in next-generation sequencing-based measurement techniques. Statistical analysis and the validity of conclusions drawn from (time series) 16S rRNA and other metagenomic sequencing data is hamper...

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Autores principales: Äijö, Tarmo, Müller, Christian L, Bonneau, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860357/
https://www.ncbi.nlm.nih.gov/pubmed/28968799
http://dx.doi.org/10.1093/bioinformatics/btx549
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author Äijö, Tarmo
Müller, Christian L
Bonneau, Richard
author_facet Äijö, Tarmo
Müller, Christian L
Bonneau, Richard
author_sort Äijö, Tarmo
collection PubMed
description MOTIVATION: The number of microbial and metagenomic studies has increased drastically due to advancements in next-generation sequencing-based measurement techniques. Statistical analysis and the validity of conclusions drawn from (time series) 16S rRNA and other metagenomic sequencing data is hampered by the presence of significant amount of noise and missing data (sampling zeros). Accounting uncertainty in microbiome data is often challenging due to the difficulty of obtaining biological replicates. Additionally, the compositional nature of current amplicon and metagenomic data differs from many other biological data types adding another challenge to the data analysis. RESULTS: To address these challenges in human microbiome research, we introduce a novel probabilistic approach to explicitly model overdispersion and sampling zeros by considering the temporal correlation between nearby time points using Gaussian Processes. The proposed Temporal Gaussian Process Model for Compositional Data Analysis (TGP-CODA) shows superior modeling performance compared to commonly used Dirichlet-multinomial, multinomial and non-parametric regression models on real and synthetic data. We demonstrate that the nonreplicative nature of human gut microbiota studies can be partially overcome by our method with proper experimental design of dense temporal sampling. We also show that different modeling approaches have a strong impact on ecological interpretation of the data, such as stationarity, persistence and environmental noise models. AVAILABILITY AND IMPLEMENTATION: A Stan implementation of the proposed method is available under MIT license at https://github.com/tare/GPMicrobiome. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-58603572018-03-21 Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing Äijö, Tarmo Müller, Christian L Bonneau, Richard Bioinformatics Original Papers MOTIVATION: The number of microbial and metagenomic studies has increased drastically due to advancements in next-generation sequencing-based measurement techniques. Statistical analysis and the validity of conclusions drawn from (time series) 16S rRNA and other metagenomic sequencing data is hampered by the presence of significant amount of noise and missing data (sampling zeros). Accounting uncertainty in microbiome data is often challenging due to the difficulty of obtaining biological replicates. Additionally, the compositional nature of current amplicon and metagenomic data differs from many other biological data types adding another challenge to the data analysis. RESULTS: To address these challenges in human microbiome research, we introduce a novel probabilistic approach to explicitly model overdispersion and sampling zeros by considering the temporal correlation between nearby time points using Gaussian Processes. The proposed Temporal Gaussian Process Model for Compositional Data Analysis (TGP-CODA) shows superior modeling performance compared to commonly used Dirichlet-multinomial, multinomial and non-parametric regression models on real and synthetic data. We demonstrate that the nonreplicative nature of human gut microbiota studies can be partially overcome by our method with proper experimental design of dense temporal sampling. We also show that different modeling approaches have a strong impact on ecological interpretation of the data, such as stationarity, persistence and environmental noise models. AVAILABILITY AND IMPLEMENTATION: A Stan implementation of the proposed method is available under MIT license at https://github.com/tare/GPMicrobiome. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-02-01 2017-09-13 /pmc/articles/PMC5860357/ /pubmed/28968799 http://dx.doi.org/10.1093/bioinformatics/btx549 Text en © The Author 2017. 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
Äijö, Tarmo
Müller, Christian L
Bonneau, Richard
Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing
title Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing
title_full Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing
title_fullStr Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing
title_full_unstemmed Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing
title_short Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing
title_sort temporal probabilistic modeling of bacterial compositions derived from 16s rrna sequencing
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860357/
https://www.ncbi.nlm.nih.gov/pubmed/28968799
http://dx.doi.org/10.1093/bioinformatics/btx549
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