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Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes
BACKGROUND: Biological processes typically involve the interactions of a number of elements (genes, cells) acting on each others. Such processes are often modelled as networks whose nodes are the elements in question and edges pairwise relations between them (transcription, inhibition). But more oft...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746320/ https://www.ncbi.nlm.nih.gov/pubmed/19774090 http://dx.doi.org/10.1371/journal.pone.0006899 |
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author | Ladroue, Christophe Guo, Shuixia Kendrick, Keith Feng, Jianfeng |
author_facet | Ladroue, Christophe Guo, Shuixia Kendrick, Keith Feng, Jianfeng |
author_sort | Ladroue, Christophe |
collection | PubMed |
description | BACKGROUND: Biological processes typically involve the interactions of a number of elements (genes, cells) acting on each others. Such processes are often modelled as networks whose nodes are the elements in question and edges pairwise relations between them (transcription, inhibition). But more often than not, elements actually work cooperatively or competitively to achieve a task. Or an element can act on the interaction between two others, as in the case of an enzyme controlling a reaction rate. We call “complex” these types of interaction and propose ways to identify them from time-series observations. METHODOLOGY: We use Granger Causality, a measure of the interaction between two signals, to characterize the influence of an enzyme on a reaction rate. We extend its traditional formulation to the case of multi-dimensional signals in order to capture group interactions, and not only element interactions. Our method is extensively tested on simulated data and applied to three biological datasets: microarray data of the Saccharomyces cerevisiae yeast, local field potential recordings of two brain areas and a metabolic reaction. CONCLUSIONS: Our results demonstrate that complex Granger causality can reveal new types of relation between signals and is particularly suited to biological data. Our approach raises some fundamental issues of the systems biology approach since finding all complex causalities (interactions) is an NP hard problem. |
format | Text |
id | pubmed-2746320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27463202009-09-23 Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes Ladroue, Christophe Guo, Shuixia Kendrick, Keith Feng, Jianfeng PLoS One Research Article BACKGROUND: Biological processes typically involve the interactions of a number of elements (genes, cells) acting on each others. Such processes are often modelled as networks whose nodes are the elements in question and edges pairwise relations between them (transcription, inhibition). But more often than not, elements actually work cooperatively or competitively to achieve a task. Or an element can act on the interaction between two others, as in the case of an enzyme controlling a reaction rate. We call “complex” these types of interaction and propose ways to identify them from time-series observations. METHODOLOGY: We use Granger Causality, a measure of the interaction between two signals, to characterize the influence of an enzyme on a reaction rate. We extend its traditional formulation to the case of multi-dimensional signals in order to capture group interactions, and not only element interactions. Our method is extensively tested on simulated data and applied to three biological datasets: microarray data of the Saccharomyces cerevisiae yeast, local field potential recordings of two brain areas and a metabolic reaction. CONCLUSIONS: Our results demonstrate that complex Granger causality can reveal new types of relation between signals and is particularly suited to biological data. Our approach raises some fundamental issues of the systems biology approach since finding all complex causalities (interactions) is an NP hard problem. Public Library of Science 2009-09-23 /pmc/articles/PMC2746320/ /pubmed/19774090 http://dx.doi.org/10.1371/journal.pone.0006899 Text en Ladroue 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 Ladroue, Christophe Guo, Shuixia Kendrick, Keith Feng, Jianfeng Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes |
title | Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes |
title_full | Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes |
title_fullStr | Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes |
title_full_unstemmed | Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes |
title_short | Beyond Element-Wise Interactions: Identifying Complex Interactions in Biological Processes |
title_sort | beyond element-wise interactions: identifying complex interactions in biological processes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746320/ https://www.ncbi.nlm.nih.gov/pubmed/19774090 http://dx.doi.org/10.1371/journal.pone.0006899 |
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