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Predicting receptor-ligand pairs through kernel learning
BACKGROUND: Regulation of cellular events is, often, initiated via extracellular signaling. Extracellular signaling occurs when a circulating ligand interacts with one or more membrane-bound receptors. Identification of receptor-ligand pairs is thus an important and specific form of PPI prediction....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199765/ https://www.ncbi.nlm.nih.gov/pubmed/21834994 http://dx.doi.org/10.1186/1471-2105-12-336 |
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author | Iacucci, Ernesto Ojeda, Fabian De Moor, Bart Moreau, Yves |
author_facet | Iacucci, Ernesto Ojeda, Fabian De Moor, Bart Moreau, Yves |
author_sort | Iacucci, Ernesto |
collection | PubMed |
description | BACKGROUND: Regulation of cellular events is, often, initiated via extracellular signaling. Extracellular signaling occurs when a circulating ligand interacts with one or more membrane-bound receptors. Identification of receptor-ligand pairs is thus an important and specific form of PPI prediction. RESULTS: Given a set of disparate data sources (expression data, domain content, and phylogenetic profile) we seek to predict new receptor-ligand pairs. We create a combined kernel classifier and assess its performance with respect to the Database of Ligand-Receptor Partners (DLRP) 'golden standard' as well as the method proposed by Gertz et al. Among our findings, we discover that our predictions for the tgfβ family accurately reconstruct over 76% of the supported edges (0.76 recall and 0.67 precision) of the receptor-ligand bipartite graph defined by the DLRP "golden standard". In addition, for the tgfβ family, the combined kernel classifier is able to relatively improve upon the Gertz et al. work by a factor of approximately 1.5 when considering that our method has an F-measure of 0.71 while that of Gertz et al. has a value of 0.48. CONCLUSIONS: The prediction of receptor-ligand pairings is a difficult and complex task. We have demonstrated that using kernel learning on multiple data sources provides a stronger alternative to the existing method in solving this task. |
format | Online Article Text |
id | pubmed-3199765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31997652011-10-24 Predicting receptor-ligand pairs through kernel learning Iacucci, Ernesto Ojeda, Fabian De Moor, Bart Moreau, Yves BMC Bioinformatics Methodology Article BACKGROUND: Regulation of cellular events is, often, initiated via extracellular signaling. Extracellular signaling occurs when a circulating ligand interacts with one or more membrane-bound receptors. Identification of receptor-ligand pairs is thus an important and specific form of PPI prediction. RESULTS: Given a set of disparate data sources (expression data, domain content, and phylogenetic profile) we seek to predict new receptor-ligand pairs. We create a combined kernel classifier and assess its performance with respect to the Database of Ligand-Receptor Partners (DLRP) 'golden standard' as well as the method proposed by Gertz et al. Among our findings, we discover that our predictions for the tgfβ family accurately reconstruct over 76% of the supported edges (0.76 recall and 0.67 precision) of the receptor-ligand bipartite graph defined by the DLRP "golden standard". In addition, for the tgfβ family, the combined kernel classifier is able to relatively improve upon the Gertz et al. work by a factor of approximately 1.5 when considering that our method has an F-measure of 0.71 while that of Gertz et al. has a value of 0.48. CONCLUSIONS: The prediction of receptor-ligand pairings is a difficult and complex task. We have demonstrated that using kernel learning on multiple data sources provides a stronger alternative to the existing method in solving this task. BioMed Central 2011-08-11 /pmc/articles/PMC3199765/ /pubmed/21834994 http://dx.doi.org/10.1186/1471-2105-12-336 Text en Copyright ©2011 Iacucci 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 | Methodology Article Iacucci, Ernesto Ojeda, Fabian De Moor, Bart Moreau, Yves Predicting receptor-ligand pairs through kernel learning |
title | Predicting receptor-ligand pairs through kernel learning |
title_full | Predicting receptor-ligand pairs through kernel learning |
title_fullStr | Predicting receptor-ligand pairs through kernel learning |
title_full_unstemmed | Predicting receptor-ligand pairs through kernel learning |
title_short | Predicting receptor-ligand pairs through kernel learning |
title_sort | predicting receptor-ligand pairs through kernel learning |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199765/ https://www.ncbi.nlm.nih.gov/pubmed/21834994 http://dx.doi.org/10.1186/1471-2105-12-336 |
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