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Evaluating eukaryotic secreted protein prediction

BACKGROUND: Improvements in protein sequence annotation and an increase in the number of annotated protein databases has fueled development of an increasing number of software tools to predict secreted proteins. Six software programs capable of high throughput and employing a wide range of predictio...

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Detalles Bibliográficos
Autores principales: Klee, Eric W, Ellis, Lynda BM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1276785/
https://www.ncbi.nlm.nih.gov/pubmed/16225690
http://dx.doi.org/10.1186/1471-2105-6-256
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author Klee, Eric W
Ellis, Lynda BM
author_facet Klee, Eric W
Ellis, Lynda BM
author_sort Klee, Eric W
collection PubMed
description BACKGROUND: Improvements in protein sequence annotation and an increase in the number of annotated protein databases has fueled development of an increasing number of software tools to predict secreted proteins. Six software programs capable of high throughput and employing a wide range of prediction methods, SignalP 3.0, SignalP 2.0, TargetP 1.01, PrediSi, Phobius, and ProtComp 6.0, are evaluated. RESULTS: Prediction accuracies were evaluated using 372 unbiased, eukaryotic, SwissProt protein sequences. TargetP, SignalP 3.0 maximum S-score and SignalP 3.0 D-score were the most accurate single scores (90–91% accurate). The combination of a positive TargetP prediction, SignalP 2.0 maximum Y-score, and SignalP 3.0 maximum S-score increased accuracy by six percent. CONCLUSION: Single predictive scores could be highly accurate, but almost all accuracies were slightly less than those reported by program authors. Predictive accuracy could be substantially improved by combining scores from multiple methods into a single composite prediction.
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spelling pubmed-12767852005-11-03 Evaluating eukaryotic secreted protein prediction Klee, Eric W Ellis, Lynda BM BMC Bioinformatics Research Article BACKGROUND: Improvements in protein sequence annotation and an increase in the number of annotated protein databases has fueled development of an increasing number of software tools to predict secreted proteins. Six software programs capable of high throughput and employing a wide range of prediction methods, SignalP 3.0, SignalP 2.0, TargetP 1.01, PrediSi, Phobius, and ProtComp 6.0, are evaluated. RESULTS: Prediction accuracies were evaluated using 372 unbiased, eukaryotic, SwissProt protein sequences. TargetP, SignalP 3.0 maximum S-score and SignalP 3.0 D-score were the most accurate single scores (90–91% accurate). The combination of a positive TargetP prediction, SignalP 2.0 maximum Y-score, and SignalP 3.0 maximum S-score increased accuracy by six percent. CONCLUSION: Single predictive scores could be highly accurate, but almost all accuracies were slightly less than those reported by program authors. Predictive accuracy could be substantially improved by combining scores from multiple methods into a single composite prediction. BioMed Central 2005-10-14 /pmc/articles/PMC1276785/ /pubmed/16225690 http://dx.doi.org/10.1186/1471-2105-6-256 Text en Copyright © 2005 Klee and Ellis; 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 Article
Klee, Eric W
Ellis, Lynda BM
Evaluating eukaryotic secreted protein prediction
title Evaluating eukaryotic secreted protein prediction
title_full Evaluating eukaryotic secreted protein prediction
title_fullStr Evaluating eukaryotic secreted protein prediction
title_full_unstemmed Evaluating eukaryotic secreted protein prediction
title_short Evaluating eukaryotic secreted protein prediction
title_sort evaluating eukaryotic secreted protein prediction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1276785/
https://www.ncbi.nlm.nih.gov/pubmed/16225690
http://dx.doi.org/10.1186/1471-2105-6-256
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