Discriminative topological features reveal biological network mechanisms

<p>Abstract</p> <p>Background</p> <p>Recent genomic and bioinformatic advances have motivated the development of numerous network models intending to describe graphs of biological, technological, and sociological origin. In most cases the success of a model has been eva...

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Main Authors: Levovitz Chaya, Koytcheff Robin, Hom Jen, Adams Carter, Ziv Etay, Middendorf Manuel, Woods Gregory, Chen Linda, Wiggins Chris
Format: Article
Language:English
Published: BMC 2004-11-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/5/181
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spelling doaj-1adbb850412d4820b318a472a81e09712020-11-24T21:04:37ZengBMCBMC Bioinformatics1471-21052004-11-015118110.1186/1471-2105-5-181Discriminative topological features reveal biological network mechanismsLevovitz ChayaKoytcheff RobinHom JenAdams CarterZiv EtayMiddendorf ManuelWoods GregoryChen LindaWiggins Chris<p>Abstract</p> <p>Background</p> <p>Recent genomic and bioinformatic advances have motivated the development of numerous network models intending to describe graphs of biological, technological, and sociological origin. In most cases the success of a model has been evaluated by how well it reproduces a few key features of the real-world data, such as degree distributions, mean geodesic lengths, and clustering coefficients. Often pairs of models can reproduce these features with indistinguishable fidelity despite being generated by vastly different mechanisms. In such cases, these few target features are insufficient to distinguish which of the different models best describes real world networks of interest; moreover, it is not clear a priori that <it>any </it>of the presently-existing algorithms for network generation offers a predictive description of the networks inspiring them.</p> <p>Results</p> <p>We present a method to assess systematically which of a set of proposed network generation algorithms gives the most accurate description of a given biological network. To derive discriminative classifiers, we construct a mapping from the set of all graphs to a high-dimensional (in principle infinite-dimensional) "word space". This map defines an input space for classification schemes which allow us to state unambiguously which models are most descriptive of a given network of interest. Our training sets include networks generated from 17 models either drawn from the literature or introduced in this work. We show that different duplication-mutation schemes best describe the <it>E. coli </it>genetic network, the <it>S. cerevisiae </it>protein interaction network, and the <it>C. elegans </it>neuronal network, out of a set of network models including a linear preferential attachment model and a small-world model.</p> <p>Conclusions</p> <p>Our method is a first step towards systematizing network models and assessing their predictability, and we anticipate its usefulness for a number of communities.</p> http://www.biomedcentral.com/1471-2105/5/181
collection DOAJ
language English
format Article
sources DOAJ
author Levovitz Chaya
Koytcheff Robin
Hom Jen
Adams Carter
Ziv Etay
Middendorf Manuel
Woods Gregory
Chen Linda
Wiggins Chris
spellingShingle Levovitz Chaya
Koytcheff Robin
Hom Jen
Adams Carter
Ziv Etay
Middendorf Manuel
Woods Gregory
Chen Linda
Wiggins Chris
Discriminative topological features reveal biological network mechanisms
BMC Bioinformatics
author_facet Levovitz Chaya
Koytcheff Robin
Hom Jen
Adams Carter
Ziv Etay
Middendorf Manuel
Woods Gregory
Chen Linda
Wiggins Chris
author_sort Levovitz Chaya
title Discriminative topological features reveal biological network mechanisms
title_short Discriminative topological features reveal biological network mechanisms
title_full Discriminative topological features reveal biological network mechanisms
title_fullStr Discriminative topological features reveal biological network mechanisms
title_full_unstemmed Discriminative topological features reveal biological network mechanisms
title_sort discriminative topological features reveal biological network mechanisms
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2004-11-01
description <p>Abstract</p> <p>Background</p> <p>Recent genomic and bioinformatic advances have motivated the development of numerous network models intending to describe graphs of biological, technological, and sociological origin. In most cases the success of a model has been evaluated by how well it reproduces a few key features of the real-world data, such as degree distributions, mean geodesic lengths, and clustering coefficients. Often pairs of models can reproduce these features with indistinguishable fidelity despite being generated by vastly different mechanisms. In such cases, these few target features are insufficient to distinguish which of the different models best describes real world networks of interest; moreover, it is not clear a priori that <it>any </it>of the presently-existing algorithms for network generation offers a predictive description of the networks inspiring them.</p> <p>Results</p> <p>We present a method to assess systematically which of a set of proposed network generation algorithms gives the most accurate description of a given biological network. To derive discriminative classifiers, we construct a mapping from the set of all graphs to a high-dimensional (in principle infinite-dimensional) "word space". This map defines an input space for classification schemes which allow us to state unambiguously which models are most descriptive of a given network of interest. Our training sets include networks generated from 17 models either drawn from the literature or introduced in this work. We show that different duplication-mutation schemes best describe the <it>E. coli </it>genetic network, the <it>S. cerevisiae </it>protein interaction network, and the <it>C. elegans </it>neuronal network, out of a set of network models including a linear preferential attachment model and a small-world model.</p> <p>Conclusions</p> <p>Our method is a first step towards systematizing network models and assessing their predictability, and we anticipate its usefulness for a number of communities.</p>
url http://www.biomedcentral.com/1471-2105/5/181
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