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High-dimensional linear state space models for dynamic microbial interaction networks
Medical researchers are increasingly interested in knowing how the complex community of micro-organisms living on human body impacts human health. Key to this is to understand how the microbes interact with each other. Time-course studies on human microbiome indicate that the composition of microbio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687744/ https://www.ncbi.nlm.nih.gov/pubmed/29141044 http://dx.doi.org/10.1371/journal.pone.0187822 |
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author | Chen, Iris Kelkar, Yogeshwar D. Gu, Yu Zhou, Jie Qiu, Xing Wu, Hulin |
author_facet | Chen, Iris Kelkar, Yogeshwar D. Gu, Yu Zhou, Jie Qiu, Xing Wu, Hulin |
author_sort | Chen, Iris |
collection | PubMed |
description | Medical researchers are increasingly interested in knowing how the complex community of micro-organisms living on human body impacts human health. Key to this is to understand how the microbes interact with each other. Time-course studies on human microbiome indicate that the composition of microbiome changes over short time periods, primarily as a consequence of synergistic and antagonistic interactions of the members of the microbiome with each other and with the environment. Knowledge of the abundance of bacteria—which are the predominant members of the human microbiome—in such time-course studies along with appropriate mathematical models will allow us to identify key dynamic interaction networks within the microbiome. However, the high-dimensional nature of these data poses significant challenges to the development of such mathematical models. We propose a high-dimensional linear State Space Model (SSM) with a new Expectation-Regularization-Maximization (ERM) algorithm to construct a dynamic Microbial Interaction Network (MIN). System noise and measurement noise can be separately specified through SSMs. In order to deal with the problem of high-dimensional parameter space in the SSMs, the proposed new ERM algorithm employs the idea of the adaptive LASSO-based variable selection method so that the sparsity property of MINs can be preserved. We performed simulation studies to evaluate the proposed ERM algorithm for variable selection. The proposed method is applied to identify the dynamic MIN from a time-course vaginal microbiome study of women. This method is amenable to future developments, which may include interactions between microbes and the environment. |
format | Online Article Text |
id | pubmed-5687744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56877442017-11-30 High-dimensional linear state space models for dynamic microbial interaction networks Chen, Iris Kelkar, Yogeshwar D. Gu, Yu Zhou, Jie Qiu, Xing Wu, Hulin PLoS One Research Article Medical researchers are increasingly interested in knowing how the complex community of micro-organisms living on human body impacts human health. Key to this is to understand how the microbes interact with each other. Time-course studies on human microbiome indicate that the composition of microbiome changes over short time periods, primarily as a consequence of synergistic and antagonistic interactions of the members of the microbiome with each other and with the environment. Knowledge of the abundance of bacteria—which are the predominant members of the human microbiome—in such time-course studies along with appropriate mathematical models will allow us to identify key dynamic interaction networks within the microbiome. However, the high-dimensional nature of these data poses significant challenges to the development of such mathematical models. We propose a high-dimensional linear State Space Model (SSM) with a new Expectation-Regularization-Maximization (ERM) algorithm to construct a dynamic Microbial Interaction Network (MIN). System noise and measurement noise can be separately specified through SSMs. In order to deal with the problem of high-dimensional parameter space in the SSMs, the proposed new ERM algorithm employs the idea of the adaptive LASSO-based variable selection method so that the sparsity property of MINs can be preserved. We performed simulation studies to evaluate the proposed ERM algorithm for variable selection. The proposed method is applied to identify the dynamic MIN from a time-course vaginal microbiome study of women. This method is amenable to future developments, which may include interactions between microbes and the environment. Public Library of Science 2017-11-15 /pmc/articles/PMC5687744/ /pubmed/29141044 http://dx.doi.org/10.1371/journal.pone.0187822 Text en © 2017 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chen, Iris Kelkar, Yogeshwar D. Gu, Yu Zhou, Jie Qiu, Xing Wu, Hulin High-dimensional linear state space models for dynamic microbial interaction networks |
title | High-dimensional linear state space models for dynamic microbial interaction networks |
title_full | High-dimensional linear state space models for dynamic microbial interaction networks |
title_fullStr | High-dimensional linear state space models for dynamic microbial interaction networks |
title_full_unstemmed | High-dimensional linear state space models for dynamic microbial interaction networks |
title_short | High-dimensional linear state space models for dynamic microbial interaction networks |
title_sort | high-dimensional linear state space models for dynamic microbial interaction networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687744/ https://www.ncbi.nlm.nih.gov/pubmed/29141044 http://dx.doi.org/10.1371/journal.pone.0187822 |
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