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Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes
BACKGROUND: The vast majority of microbiome research so far has focused on the structure of the microbiome at a single time-point. There have been several studies that measure the microbiome from a particular environment over time. A few models have been developed by extending time series models to...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549249/ https://www.ncbi.nlm.nih.gov/pubmed/33045987 http://dx.doi.org/10.1186/s12859-020-03747-4 |
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author | Kenney, Toby Gao, Junqiu Gu, Hong |
author_facet | Kenney, Toby Gao, Junqiu Gu, Hong |
author_sort | Kenney, Toby |
collection | PubMed |
description | BACKGROUND: The vast majority of microbiome research so far has focused on the structure of the microbiome at a single time-point. There have been several studies that measure the microbiome from a particular environment over time. A few models have been developed by extending time series models to accomodate specific features in microbiome data to address questions of stability and interactions of the microbime time series. Most research has observed the stability and mean reversion for some microbiomes. However, little has been done to study the mean reversion rates of these stable microbes and how sampling frequencies are related to such conclusions. In this paper, we begin to rectify this situation. We analyse two widely studied microbial time series data sets on four healthy individuals. We choose to study healthy individuals because we are interested in the baseline temporal dynamics of the microbiome. RESULTS: For this analysis, we focus on the temporal dynamics of individual genera, absorbing all interactions in a stochastic term. We use a simple stochastic differential equation model to assess the following three questions. (1) Does the microbiome exhibit temporal continuity? (2) Does the microbiome have a stable state? (3) To better understand the temporal dynamics, how frequently should data be sampled in future studies? We find that a simple Ornstein–Uhlenbeck model which incorporates both temporal continuity and reversion to a stable state fits the data for almost every genus better than a Brownian motion model that contains only temporal continuity. The Ornstein–Uhlenbeck model also fits the data better than modelling separate time points as independent. Under the Ornstein–Uhlenbeck model, we calculate the variance of the estimated mean reversion rate (the speed with which each genus returns to its stable state). Based on this calculation, we are able to determine the optimal sample schemes for studying temporal dynamics. CONCLUSIONS: There is evidence of temporal continuity for most genera; there is clear evidence of a stable state; and the optimal sampling frequency for studying temporal dynamics is in the range of one sample every 0.8–3.2 days. |
format | Online Article Text |
id | pubmed-7549249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75492492020-10-13 Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes Kenney, Toby Gao, Junqiu Gu, Hong BMC Bioinformatics Research Article BACKGROUND: The vast majority of microbiome research so far has focused on the structure of the microbiome at a single time-point. There have been several studies that measure the microbiome from a particular environment over time. A few models have been developed by extending time series models to accomodate specific features in microbiome data to address questions of stability and interactions of the microbime time series. Most research has observed the stability and mean reversion for some microbiomes. However, little has been done to study the mean reversion rates of these stable microbes and how sampling frequencies are related to such conclusions. In this paper, we begin to rectify this situation. We analyse two widely studied microbial time series data sets on four healthy individuals. We choose to study healthy individuals because we are interested in the baseline temporal dynamics of the microbiome. RESULTS: For this analysis, we focus on the temporal dynamics of individual genera, absorbing all interactions in a stochastic term. We use a simple stochastic differential equation model to assess the following three questions. (1) Does the microbiome exhibit temporal continuity? (2) Does the microbiome have a stable state? (3) To better understand the temporal dynamics, how frequently should data be sampled in future studies? We find that a simple Ornstein–Uhlenbeck model which incorporates both temporal continuity and reversion to a stable state fits the data for almost every genus better than a Brownian motion model that contains only temporal continuity. The Ornstein–Uhlenbeck model also fits the data better than modelling separate time points as independent. Under the Ornstein–Uhlenbeck model, we calculate the variance of the estimated mean reversion rate (the speed with which each genus returns to its stable state). Based on this calculation, we are able to determine the optimal sample schemes for studying temporal dynamics. CONCLUSIONS: There is evidence of temporal continuity for most genera; there is clear evidence of a stable state; and the optimal sampling frequency for studying temporal dynamics is in the range of one sample every 0.8–3.2 days. BioMed Central 2020-10-12 /pmc/articles/PMC7549249/ /pubmed/33045987 http://dx.doi.org/10.1186/s12859-020-03747-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Kenney, Toby Gao, Junqiu Gu, Hong Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
title | Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
title_full | Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
title_fullStr | Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
title_full_unstemmed | Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
title_short | Application of OU processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
title_sort | application of ou processes to modelling temporal dynamics of the human microbiome, and calculating optimal sampling schemes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549249/ https://www.ncbi.nlm.nih.gov/pubmed/33045987 http://dx.doi.org/10.1186/s12859-020-03747-4 |
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