Is it better to combine predictions?

Published

Journal Article

We have compared the accuracy of the individual protein secondary structure prediction methods: PHD, DSC, NNSSP and Predator against the accuracy obtained by combing the predictions of the methods. A range of ways of combing predictions were tested: voting, biased voting, linear discrimination, neural networks and decision trees. The combined methods that involve 'learning' (the non-voting methods) were trained using a set of 496 non-homologous domains; this dataset was biased as some of the secondary structure prediction methods had used them for training. We used two independent test sets to compare predictions: the first consisted of 17 non-homologous domains from CASP3 (Third Community Wide Experiment on the Critical Assessment of Techniques for Protein Structure Prediction); the second set consisted of 405 domains that were selected in the same way as the training set, and were non-homologous to each other and the training set. On both test datasets the most accurate individual method was NNSSP, then PHD, DSC and the least accurate was Predator; however, it was not possible to conclusively show a significant difference between the individual methods. Comparing the accuracy of the single methods with that obtained by combing predictions it was found that it was better to use a combination of predictions. On both test datasets it was possible to obtain a approximately 3% improvement in accuracy by combing predictions. In most cases the combined methods were statistically significantly better (at P = 0.05 on the CASP3 test set, and P = 0.01 on the EBI test set). On the CASP3 test dataset there was no significant difference in accuracy between any of the combined method of prediction: on the EBI test dataset, linear discrimination and neural networks significantly outperformed voting techniques. We conclude that it is better to combine predictions.

Full Text

Duke Authors

Cited Authors

  • King, RD; Ouali, M; Strong, AT; Aly, A; Elmaghraby, A; Kantardzic, M; Page, D

Published Date

  • January 2000

Published In

Volume / Issue

  • 13 / 1

Start / End Page

  • 15 - 19

PubMed ID

  • 10679525

Pubmed Central ID

  • 10679525

International Standard Serial Number (ISSN)

  • 0269-2139

Digital Object Identifier (DOI)

  • 10.1093/protein/13.1.15

Language

  • eng

Conference Location

  • England