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Is bagging effective in the classification of small-sample genomic and proteomic data?
1Department of Electrical and Computer Engineering, Texas A&M University, College Station, TX 77843-3128, USA.
EURASIP Journal on Bioinformatics & Systems Biology
|April 25, 2009
Summary
Bagging improves unstable classifiers for gene and protein data but does not outperform stable classifiers. This ensemble method shows limited practical benefit for small-sample genomic and proteomic datasets.
Area of Science:
- Bioinformatics
- Computational Biology
- Machine Learning in Genomics
Background:
- Bagging is frequently applied to gene-expression and protein-abundance mass spectrometry data classification.
- The justification is often improved performance of unstable, overfitting classifiers in small-sample scenarios.
Purpose of the Study:
- To determine if bagging sufficiently improves classifier performance to surpass stable, nonoverfitting classifiers for small-sample genomic and proteomic data.
- To evaluate the practical utility of ensemble methods in this context.
Main Methods:
- Empirical study using publicly available genomic and proteomic datasets.
- Feature selection using t-test and RELIEF.
- Comparison of bagging with stable classifiers like linear discriminant analysis and 3-nearest neighbors.
Main Results:
- Bagging improved unstable classifiers (CART, neural networks) but not enough to outperform stable classifiers (linear discriminant analysis, 3-nearest neighbors).
- Ensemble methods did not significantly enhance the performance of already stable classifiers.
Conclusions:
- While bagging enhances unstable classifiers, it does not provide a practical advantage over stable classifiers for small-sample genomic and proteomic data analysis.
- The study questions the widespread applicability of bagging for these specific data types and sample sizes.

