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Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q)
BACKGROUND: Gene clustering of periodic transcriptional profiles provides an opportunity to shed light on a variety of biological processes, but this technique relies critically upon the robust modeling of longitudinal covariance structure over time. METHODOLOGY: We propose a statistical method for...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855703/ https://www.ncbi.nlm.nih.gov/pubmed/20419127 http://dx.doi.org/10.1371/journal.pone.0009894 |
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author | Li, Ning McMurry, Timothy Berg, Arthur Wang, Zhong Berceli, Scott A. Wu, Rongling |
author_facet | Li, Ning McMurry, Timothy Berg, Arthur Wang, Zhong Berceli, Scott A. Wu, Rongling |
author_sort | Li, Ning |
collection | PubMed |
description | BACKGROUND: Gene clustering of periodic transcriptional profiles provides an opportunity to shed light on a variety of biological processes, but this technique relies critically upon the robust modeling of longitudinal covariance structure over time. METHODOLOGY: We propose a statistical method for functional clustering of periodic gene expression by modeling the covariance matrix of serial measurements through a general autoregressive moving-average process of order ([Image: see text],[Image: see text]), the so-called ARMA([Image: see text],[Image: see text]). We derive a sophisticated EM algorithm to estimate the proportions of each gene cluster, the Fourier series parameters that define gene-specific differences in periodic expression trajectories, and the ARMA parameters that model the covariance structure within a mixture model framework. The orders [Image: see text] and [Image: see text] of the ARMA process that provide the best fit are identified by model selection criteria. CONCLUSIONS: Through simulated data we show that whenever it is necessary, employment of sophisticated covariance structures such as ARMA is crucial in order to obtain unbiased estimates of the mean structure parameters and increased precision of estimation. The methods were implemented on recently published time-course gene expression data in yeast and the procedure was shown to effectively identify interesting periodic clusters in the dataset. The new approach will provide a powerful tool for understanding biological functions on a genomic scale. |
format | Text |
id | pubmed-2855703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28557032010-04-23 Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) Li, Ning McMurry, Timothy Berg, Arthur Wang, Zhong Berceli, Scott A. Wu, Rongling PLoS One Research Article BACKGROUND: Gene clustering of periodic transcriptional profiles provides an opportunity to shed light on a variety of biological processes, but this technique relies critically upon the robust modeling of longitudinal covariance structure over time. METHODOLOGY: We propose a statistical method for functional clustering of periodic gene expression by modeling the covariance matrix of serial measurements through a general autoregressive moving-average process of order ([Image: see text],[Image: see text]), the so-called ARMA([Image: see text],[Image: see text]). We derive a sophisticated EM algorithm to estimate the proportions of each gene cluster, the Fourier series parameters that define gene-specific differences in periodic expression trajectories, and the ARMA parameters that model the covariance structure within a mixture model framework. The orders [Image: see text] and [Image: see text] of the ARMA process that provide the best fit are identified by model selection criteria. CONCLUSIONS: Through simulated data we show that whenever it is necessary, employment of sophisticated covariance structures such as ARMA is crucial in order to obtain unbiased estimates of the mean structure parameters and increased precision of estimation. The methods were implemented on recently published time-course gene expression data in yeast and the procedure was shown to effectively identify interesting periodic clusters in the dataset. The new approach will provide a powerful tool for understanding biological functions on a genomic scale. Public Library of Science 2010-04-16 /pmc/articles/PMC2855703/ /pubmed/20419127 http://dx.doi.org/10.1371/journal.pone.0009894 Text en Li 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Li, Ning McMurry, Timothy Berg, Arthur Wang, Zhong Berceli, Scott A. Wu, Rongling Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) |
title | Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) |
title_full | Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) |
title_fullStr | Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) |
title_full_unstemmed | Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) |
title_short | Functional Clustering of Periodic Transcriptional Profiles through ARMA(p,q) |
title_sort | functional clustering of periodic transcriptional profiles through arma(p,q) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855703/ https://www.ncbi.nlm.nih.gov/pubmed/20419127 http://dx.doi.org/10.1371/journal.pone.0009894 |
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