Piecewise multivariate modelling of sequential metabolic profiling data

<p>Abstract</p> <p>Background</p> <p>Modelling the time-related behaviour of biological systems is essential for understanding their dynamic responses to perturbations. In metabolic profiling studies, the sampling rate and number of sampling points are often restricted...

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Main Authors: Nicholson Jeremy K, Lundstedt Torbjörn, Ebbels Timothy MD, Cloarec Olivier, Rantalainen Mattias, Holmes Elaine, Trygg Johan
Format: Article
Language:English
Published: BMC 2008-02-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/9/105
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spelling doaj-953c288bc1a64112bf83e8dddceaa5e82020-11-25T01:41:37ZengBMCBMC Bioinformatics1471-21052008-02-019110510.1186/1471-2105-9-105Piecewise multivariate modelling of sequential metabolic profiling dataNicholson Jeremy KLundstedt TorbjörnEbbels Timothy MDCloarec OlivierRantalainen MattiasHolmes ElaineTrygg Johan<p>Abstract</p> <p>Background</p> <p>Modelling the time-related behaviour of biological systems is essential for understanding their dynamic responses to perturbations. In metabolic profiling studies, the sampling rate and number of sampling points are often restricted due to experimental and biological constraints.</p> <p>Results</p> <p>A supervised multivariate modelling approach with the objective to model the time-related variation in the data for short and sparsely sampled time-series is described. A set of piecewise Orthogonal Projections to Latent Structures (OPLS) models are estimated, describing changes between successive time points. The individual OPLS models are linear, but the piecewise combination of several models accommodates modelling and prediction of changes which are non-linear with respect to the time course. We demonstrate the method on both simulated and metabolic profiling data, illustrating how time related changes are successfully modelled and predicted.</p> <p>Conclusion</p> <p>The proposed method is effective for modelling and prediction of short and multivariate time series data. A key advantage of the method is model transparency, allowing easy interpretation of time-related variation in the data. The method provides a competitive complement to commonly applied multivariate methods such as OPLS and Principal Component Analysis (PCA) for modelling and analysis of short time-series data.</p> http://www.biomedcentral.com/1471-2105/9/105
collection DOAJ
language English
format Article
sources DOAJ
author Nicholson Jeremy K
Lundstedt Torbjörn
Ebbels Timothy MD
Cloarec Olivier
Rantalainen Mattias
Holmes Elaine
Trygg Johan
spellingShingle Nicholson Jeremy K
Lundstedt Torbjörn
Ebbels Timothy MD
Cloarec Olivier
Rantalainen Mattias
Holmes Elaine
Trygg Johan
Piecewise multivariate modelling of sequential metabolic profiling data
BMC Bioinformatics
author_facet Nicholson Jeremy K
Lundstedt Torbjörn
Ebbels Timothy MD
Cloarec Olivier
Rantalainen Mattias
Holmes Elaine
Trygg Johan
author_sort Nicholson Jeremy K
title Piecewise multivariate modelling of sequential metabolic profiling data
title_short Piecewise multivariate modelling of sequential metabolic profiling data
title_full Piecewise multivariate modelling of sequential metabolic profiling data
title_fullStr Piecewise multivariate modelling of sequential metabolic profiling data
title_full_unstemmed Piecewise multivariate modelling of sequential metabolic profiling data
title_sort piecewise multivariate modelling of sequential metabolic profiling data
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2008-02-01
description <p>Abstract</p> <p>Background</p> <p>Modelling the time-related behaviour of biological systems is essential for understanding their dynamic responses to perturbations. In metabolic profiling studies, the sampling rate and number of sampling points are often restricted due to experimental and biological constraints.</p> <p>Results</p> <p>A supervised multivariate modelling approach with the objective to model the time-related variation in the data for short and sparsely sampled time-series is described. A set of piecewise Orthogonal Projections to Latent Structures (OPLS) models are estimated, describing changes between successive time points. The individual OPLS models are linear, but the piecewise combination of several models accommodates modelling and prediction of changes which are non-linear with respect to the time course. We demonstrate the method on both simulated and metabolic profiling data, illustrating how time related changes are successfully modelled and predicted.</p> <p>Conclusion</p> <p>The proposed method is effective for modelling and prediction of short and multivariate time series data. A key advantage of the method is model transparency, allowing easy interpretation of time-related variation in the data. The method provides a competitive complement to commonly applied multivariate methods such as OPLS and Principal Component Analysis (PCA) for modelling and analysis of short time-series data.</p>
url http://www.biomedcentral.com/1471-2105/9/105
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