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Information assessment on predicting protein-protein interactions
BACKGROUND: Identifying protein-protein interactions is fundamental for understanding the molecular machinery of the cell. Proteome-wide studies of protein-protein interactions are of significant value, but the high-throughput experimental technologies suffer from high rates of both false positive a...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC529436/ https://www.ncbi.nlm.nih.gov/pubmed/15491499 http://dx.doi.org/10.1186/1471-2105-5-154 |
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author | Lin, Nan Wu, Baolin Jansen, Ronald Gerstein, Mark Zhao, Hongyu |
author_facet | Lin, Nan Wu, Baolin Jansen, Ronald Gerstein, Mark Zhao, Hongyu |
author_sort | Lin, Nan |
collection | PubMed |
description | BACKGROUND: Identifying protein-protein interactions is fundamental for understanding the molecular machinery of the cell. Proteome-wide studies of protein-protein interactions are of significant value, but the high-throughput experimental technologies suffer from high rates of both false positive and false negative predictions. In addition to high-throughput experimental data, many diverse types of genomic data can help predict protein-protein interactions, such as mRNA expression, localization, essentiality, and functional annotation. Evaluations of the information contributions from different evidences help to establish more parsimonious models with comparable or better prediction accuracy, and to obtain biological insights of the relationships between protein-protein interactions and other genomic information. RESULTS: Our assessment is based on the genomic features used in a Bayesian network approach to predict protein-protein interactions genome-wide in yeast. In the special case, when one does not have any missing information about any of the features, our analysis shows that there is a larger information contribution from the functional-classification than from expression correlations or essentiality. We also show that in this case alternative models, such as logistic regression and random forest, may be more effective than Bayesian networks for predicting interactions. CONCLUSIONS: In the restricted problem posed by the complete-information subset, we identified that the MIPS and Gene Ontology (GO) functional similarity datasets as the dominating information contributors for predicting the protein-protein interactions under the framework proposed by Jansen et al. Random forests based on the MIPS and GO information alone can give highly accurate classifications. In this particular subset of complete information, adding other genomic data does little for improving predictions. We also found that the data discretizations used in the Bayesian methods decreased classification performance. |
format | Text |
id | pubmed-529436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5294362004-11-21 Information assessment on predicting protein-protein interactions Lin, Nan Wu, Baolin Jansen, Ronald Gerstein, Mark Zhao, Hongyu BMC Bioinformatics Research Article BACKGROUND: Identifying protein-protein interactions is fundamental for understanding the molecular machinery of the cell. Proteome-wide studies of protein-protein interactions are of significant value, but the high-throughput experimental technologies suffer from high rates of both false positive and false negative predictions. In addition to high-throughput experimental data, many diverse types of genomic data can help predict protein-protein interactions, such as mRNA expression, localization, essentiality, and functional annotation. Evaluations of the information contributions from different evidences help to establish more parsimonious models with comparable or better prediction accuracy, and to obtain biological insights of the relationships between protein-protein interactions and other genomic information. RESULTS: Our assessment is based on the genomic features used in a Bayesian network approach to predict protein-protein interactions genome-wide in yeast. In the special case, when one does not have any missing information about any of the features, our analysis shows that there is a larger information contribution from the functional-classification than from expression correlations or essentiality. We also show that in this case alternative models, such as logistic regression and random forest, may be more effective than Bayesian networks for predicting interactions. CONCLUSIONS: In the restricted problem posed by the complete-information subset, we identified that the MIPS and Gene Ontology (GO) functional similarity datasets as the dominating information contributors for predicting the protein-protein interactions under the framework proposed by Jansen et al. Random forests based on the MIPS and GO information alone can give highly accurate classifications. In this particular subset of complete information, adding other genomic data does little for improving predictions. We also found that the data discretizations used in the Bayesian methods decreased classification performance. BioMed Central 2004-10-18 /pmc/articles/PMC529436/ /pubmed/15491499 http://dx.doi.org/10.1186/1471-2105-5-154 Text en Copyright © 2004 Lin et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Lin, Nan Wu, Baolin Jansen, Ronald Gerstein, Mark Zhao, Hongyu Information assessment on predicting protein-protein interactions |
title | Information assessment on predicting protein-protein interactions |
title_full | Information assessment on predicting protein-protein interactions |
title_fullStr | Information assessment on predicting protein-protein interactions |
title_full_unstemmed | Information assessment on predicting protein-protein interactions |
title_short | Information assessment on predicting protein-protein interactions |
title_sort | information assessment on predicting protein-protein interactions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC529436/ https://www.ncbi.nlm.nih.gov/pubmed/15491499 http://dx.doi.org/10.1186/1471-2105-5-154 |
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