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Network Reconstruction Using Nonparametric Additive ODE Models

Network representations of biological systems are widespread and reconstructing unknown networks from data is a focal problem for computational biologists. For example, the series of biochemical reactions in a metabolic pathway can be represented as a network, with nodes corresponding to metabolites...

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Autores principales: Henderson, James, Michailidis, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986056/
https://www.ncbi.nlm.nih.gov/pubmed/24732037
http://dx.doi.org/10.1371/journal.pone.0094003
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author Henderson, James
Michailidis, George
author_facet Henderson, James
Michailidis, George
author_sort Henderson, James
collection PubMed
description Network representations of biological systems are widespread and reconstructing unknown networks from data is a focal problem for computational biologists. For example, the series of biochemical reactions in a metabolic pathway can be represented as a network, with nodes corresponding to metabolites and edges linking reactants to products. In a different context, regulatory relationships among genes are commonly represented as directed networks with edges pointing from influential genes to their targets. Reconstructing such networks from data is a challenging problem receiving much attention in the literature. There is a particular need for approaches tailored to time-series data and not reliant on direct intervention experiments, as the former are often more readily available. In this paper, we introduce an approach to reconstructing directed networks based on dynamic systems models. Our approach generalizes commonly used ODE models based on linear or nonlinear dynamics by extending the functional class for the functions involved from parametric to nonparametric models. Concomitantly we limit the complexity by imposing an additive structure on the estimated slope functions. Thus the submodel associated with each node is a sum of univariate functions. These univariate component functions form the basis for a novel coupling metric that we define in order to quantify the strength of proposed relationships and hence rank potential edges. We show the utility of the method by reconstructing networks using simulated data from computational models for the glycolytic pathway of Lactocaccus Lactis and a gene network regulating the pluripotency of mouse embryonic stem cells. For purposes of comparison, we also assess reconstruction performance using gene networks from the DREAM challenges. We compare our method to those that similarly rely on dynamic systems models and use the results to attempt to disentangle the distinct roles of linearity, sparsity, and derivative estimation.
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spelling pubmed-39860562014-04-15 Network Reconstruction Using Nonparametric Additive ODE Models Henderson, James Michailidis, George PLoS One Research Article Network representations of biological systems are widespread and reconstructing unknown networks from data is a focal problem for computational biologists. For example, the series of biochemical reactions in a metabolic pathway can be represented as a network, with nodes corresponding to metabolites and edges linking reactants to products. In a different context, regulatory relationships among genes are commonly represented as directed networks with edges pointing from influential genes to their targets. Reconstructing such networks from data is a challenging problem receiving much attention in the literature. There is a particular need for approaches tailored to time-series data and not reliant on direct intervention experiments, as the former are often more readily available. In this paper, we introduce an approach to reconstructing directed networks based on dynamic systems models. Our approach generalizes commonly used ODE models based on linear or nonlinear dynamics by extending the functional class for the functions involved from parametric to nonparametric models. Concomitantly we limit the complexity by imposing an additive structure on the estimated slope functions. Thus the submodel associated with each node is a sum of univariate functions. These univariate component functions form the basis for a novel coupling metric that we define in order to quantify the strength of proposed relationships and hence rank potential edges. We show the utility of the method by reconstructing networks using simulated data from computational models for the glycolytic pathway of Lactocaccus Lactis and a gene network regulating the pluripotency of mouse embryonic stem cells. For purposes of comparison, we also assess reconstruction performance using gene networks from the DREAM challenges. We compare our method to those that similarly rely on dynamic systems models and use the results to attempt to disentangle the distinct roles of linearity, sparsity, and derivative estimation. Public Library of Science 2014-04-14 /pmc/articles/PMC3986056/ /pubmed/24732037 http://dx.doi.org/10.1371/journal.pone.0094003 Text en © 2014 Henderson, Michailidis 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
Henderson, James
Michailidis, George
Network Reconstruction Using Nonparametric Additive ODE Models
title Network Reconstruction Using Nonparametric Additive ODE Models
title_full Network Reconstruction Using Nonparametric Additive ODE Models
title_fullStr Network Reconstruction Using Nonparametric Additive ODE Models
title_full_unstemmed Network Reconstruction Using Nonparametric Additive ODE Models
title_short Network Reconstruction Using Nonparametric Additive ODE Models
title_sort network reconstruction using nonparametric additive ode models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986056/
https://www.ncbi.nlm.nih.gov/pubmed/24732037
http://dx.doi.org/10.1371/journal.pone.0094003
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