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Computational discovery of regulatory elements in a continuous expression space

Approaches for regulatory element discovery from gene expression data usually rely on clustering algorithms to partition the data into clusters of co-expressed genes. Gene regulatory sequences are then mined to find overrepresented motifs in each cluster. However, this ad hoc partition rarely fits t...

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Detalles Bibliográficos
Autores principales: Lajoie, Mathieu, Gascuel, Olivier, Lefort, Vincent, Bréhélin, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053739/
https://www.ncbi.nlm.nih.gov/pubmed/23186104
http://dx.doi.org/10.1186/gb-2012-13-11-r109
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author Lajoie, Mathieu
Gascuel, Olivier
Lefort, Vincent
Bréhélin, Laurent
author_facet Lajoie, Mathieu
Gascuel, Olivier
Lefort, Vincent
Bréhélin, Laurent
author_sort Lajoie, Mathieu
collection PubMed
description Approaches for regulatory element discovery from gene expression data usually rely on clustering algorithms to partition the data into clusters of co-expressed genes. Gene regulatory sequences are then mined to find overrepresented motifs in each cluster. However, this ad hoc partition rarely fits the biological reality. We propose a novel method called RED(2 )that avoids data clustering by estimating motif densities locally around each gene. We show that RED(2 )detects numerous motifs not detected by clustering-based approaches, and that most of these correspond to characterized motifs. RED(2 )can be accessed online through a user-friendly interface.
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spelling pubmed-40537392014-06-16 Computational discovery of regulatory elements in a continuous expression space Lajoie, Mathieu Gascuel, Olivier Lefort, Vincent Bréhélin, Laurent Genome Biol Method Approaches for regulatory element discovery from gene expression data usually rely on clustering algorithms to partition the data into clusters of co-expressed genes. Gene regulatory sequences are then mined to find overrepresented motifs in each cluster. However, this ad hoc partition rarely fits the biological reality. We propose a novel method called RED(2 )that avoids data clustering by estimating motif densities locally around each gene. We show that RED(2 )detects numerous motifs not detected by clustering-based approaches, and that most of these correspond to characterized motifs. RED(2 )can be accessed online through a user-friendly interface. BioMed Central 2012 2012-11-27 /pmc/articles/PMC4053739/ /pubmed/23186104 http://dx.doi.org/10.1186/gb-2012-13-11-r109 Text en Copyright © 2012 Lajoie et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Lajoie, Mathieu
Gascuel, Olivier
Lefort, Vincent
Bréhélin, Laurent
Computational discovery of regulatory elements in a continuous expression space
title Computational discovery of regulatory elements in a continuous expression space
title_full Computational discovery of regulatory elements in a continuous expression space
title_fullStr Computational discovery of regulatory elements in a continuous expression space
title_full_unstemmed Computational discovery of regulatory elements in a continuous expression space
title_short Computational discovery of regulatory elements in a continuous expression space
title_sort computational discovery of regulatory elements in a continuous expression space
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053739/
https://www.ncbi.nlm.nih.gov/pubmed/23186104
http://dx.doi.org/10.1186/gb-2012-13-11-r109
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