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Choosing negative examples for the prediction of protein-protein interactions

The protein-protein interaction networks of even well-studied model organisms are sketchy at best, highlighting the continued need for computational methods to help direct experimentalists in the search for novel interactions. This need has prompted the development of a number of methods for predict...

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Detalles Bibliográficos
Autores principales: Ben-Hur, Asa, Noble, William Stafford
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810313/
https://www.ncbi.nlm.nih.gov/pubmed/16723005
http://dx.doi.org/10.1186/1471-2105-7-S1-S2
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author Ben-Hur, Asa
Noble, William Stafford
author_facet Ben-Hur, Asa
Noble, William Stafford
author_sort Ben-Hur, Asa
collection PubMed
description The protein-protein interaction networks of even well-studied model organisms are sketchy at best, highlighting the continued need for computational methods to help direct experimentalists in the search for novel interactions. This need has prompted the development of a number of methods for predicting protein-protein interactions based on various sources of data and methodologies. The common method for choosing negative examples for training a predictor of protein-protein interactions is based on annotations of cellular localization, and the observation that pairs of proteins that have different localization patterns are unlikely to interact. While this method leads to high quality sets of non-interacting proteins, we find that this choice can lead to biased estimates of prediction accuracy, because the constraints placed on the distribution of the negative examples makes the task easier. The effects of this bias are demonstrated in the context of both sequence-based and non-sequence based features used for predicting protein-protein interactions.
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spelling pubmed-18103132007-03-14 Choosing negative examples for the prediction of protein-protein interactions Ben-Hur, Asa Noble, William Stafford BMC Bioinformatics Proceedings The protein-protein interaction networks of even well-studied model organisms are sketchy at best, highlighting the continued need for computational methods to help direct experimentalists in the search for novel interactions. This need has prompted the development of a number of methods for predicting protein-protein interactions based on various sources of data and methodologies. The common method for choosing negative examples for training a predictor of protein-protein interactions is based on annotations of cellular localization, and the observation that pairs of proteins that have different localization patterns are unlikely to interact. While this method leads to high quality sets of non-interacting proteins, we find that this choice can lead to biased estimates of prediction accuracy, because the constraints placed on the distribution of the negative examples makes the task easier. The effects of this bias are demonstrated in the context of both sequence-based and non-sequence based features used for predicting protein-protein interactions. BioMed Central 2006-03-20 /pmc/articles/PMC1810313/ /pubmed/16723005 http://dx.doi.org/10.1186/1471-2105-7-S1-S2 Text en
spellingShingle Proceedings
Ben-Hur, Asa
Noble, William Stafford
Choosing negative examples for the prediction of protein-protein interactions
title Choosing negative examples for the prediction of protein-protein interactions
title_full Choosing negative examples for the prediction of protein-protein interactions
title_fullStr Choosing negative examples for the prediction of protein-protein interactions
title_full_unstemmed Choosing negative examples for the prediction of protein-protein interactions
title_short Choosing negative examples for the prediction of protein-protein interactions
title_sort choosing negative examples for the prediction of protein-protein interactions
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810313/
https://www.ncbi.nlm.nih.gov/pubmed/16723005
http://dx.doi.org/10.1186/1471-2105-7-S1-S2
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