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Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network
BACKGROUND: Despite large amounts of available genomic and proteomic data, predicting the structure and response of signaling networks is still a significant challenge. While statistical method such as Bayesian network has been explored to meet this challenge, employing existing biological knowledge...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524013/ https://www.ncbi.nlm.nih.gov/pubmed/23282239 http://dx.doi.org/10.1186/1752-0509-6-S3-S3 |
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author | Qin, Tingting Tsoi, Lam C Sims, Kellie J Lu, Xinghua Zheng, W Jim |
author_facet | Qin, Tingting Tsoi, Lam C Sims, Kellie J Lu, Xinghua Zheng, W Jim |
author_sort | Qin, Tingting |
collection | PubMed |
description | BACKGROUND: Despite large amounts of available genomic and proteomic data, predicting the structure and response of signaling networks is still a significant challenge. While statistical method such as Bayesian network has been explored to meet this challenge, employing existing biological knowledge for network prediction is difficult. The objective of this study is to develop a novel approach that integrates prior biological knowledge in the form of the Ontology Fingerprint to infer cell-type-specific signaling networks via data-driven Bayesian network learning; and to further use the trained model to predict cellular responses. RESULTS: We applied our novel approach to address the Predictive Signaling Network Modeling challenge of the fourth (2009) Dialog for Reverse Engineering Assessment's and Methods (DREAM4) competition. The challenge results showed that our method accurately captured signal transduction of a network of protein kinases and phosphoproteins in that the predicted protein phosphorylation levels under all experimental conditions were highly correlated (R(2 )= 0.93) with the observed results. Based on the evaluation of the DREAM4 organizer, our team was ranked as one of the top five best performers in predicting network structure and protein phosphorylation activity under test conditions. CONCLUSIONS: Bayesian network can be used to simulate the propagation of signals in cellular systems. Incorporating the Ontology Fingerprint as prior biological knowledge allows us to efficiently infer concise signaling network structure and to accurately predict cellular responses. |
format | Online Article Text |
id | pubmed-3524013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35240132012-12-21 Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network Qin, Tingting Tsoi, Lam C Sims, Kellie J Lu, Xinghua Zheng, W Jim BMC Syst Biol Research BACKGROUND: Despite large amounts of available genomic and proteomic data, predicting the structure and response of signaling networks is still a significant challenge. While statistical method such as Bayesian network has been explored to meet this challenge, employing existing biological knowledge for network prediction is difficult. The objective of this study is to develop a novel approach that integrates prior biological knowledge in the form of the Ontology Fingerprint to infer cell-type-specific signaling networks via data-driven Bayesian network learning; and to further use the trained model to predict cellular responses. RESULTS: We applied our novel approach to address the Predictive Signaling Network Modeling challenge of the fourth (2009) Dialog for Reverse Engineering Assessment's and Methods (DREAM4) competition. The challenge results showed that our method accurately captured signal transduction of a network of protein kinases and phosphoproteins in that the predicted protein phosphorylation levels under all experimental conditions were highly correlated (R(2 )= 0.93) with the observed results. Based on the evaluation of the DREAM4 organizer, our team was ranked as one of the top five best performers in predicting network structure and protein phosphorylation activity under test conditions. CONCLUSIONS: Bayesian network can be used to simulate the propagation of signals in cellular systems. Incorporating the Ontology Fingerprint as prior biological knowledge allows us to efficiently infer concise signaling network structure and to accurately predict cellular responses. BioMed Central 2012-12-17 /pmc/articles/PMC3524013/ /pubmed/23282239 http://dx.doi.org/10.1186/1752-0509-6-S3-S3 Text en Copyright ©2012 Qin 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 | Research Qin, Tingting Tsoi, Lam C Sims, Kellie J Lu, Xinghua Zheng, W Jim Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network |
title | Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network |
title_full | Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network |
title_fullStr | Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network |
title_full_unstemmed | Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network |
title_short | Signaling network prediction by the Ontology Fingerprint enhanced Bayesian network |
title_sort | signaling network prediction by the ontology fingerprint enhanced bayesian network |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524013/ https://www.ncbi.nlm.nih.gov/pubmed/23282239 http://dx.doi.org/10.1186/1752-0509-6-S3-S3 |
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