Dataset Information

SDED: a novel filter method for cancer-related gene selection.

ABSTRACT: Gene selection is to detect the most significantly expressed genes under different conditions expression data. The current challenge in gene selection is the comparison of a large number of genes with limited patient samples. Thus it is trivial task in simple statistical analysis. Various statistical measurements are adopted by filter methods applied in gene selection studies. Their ability to discriminate phenotypes is crucial in classification and selection. Here we describe the standard deviation error distribution (SDED) method for gene selection. It utilizes variations within-class and among-class in gene expression data. We tested the method using 4 leukemia datasets available in the public domain. The method was compared with the GS2 and CHO methods. The Prediction accuracies by SDED are better than both GS2 and CHO for different datasets. These are 0.8-4.2% and 1.6-8.4% more that in GS2 and CHO. The related OMIM annotations and KEGG pathways analyses verified that SDED can pick out more 4.0% and 6.1% genes with biological significance than GS2 and CHO, respectively.

SUBMITTER: Xu W

PROVIDER: S-EPMC2374374 | biostudies-literature | 2008 Apr

REPOSITORIES: biostudies-literature

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SDED: a novel filter method for cancer-related gene selection.

Xu Wenlong W Wang Minghui M Zhang Xianghua X Wang Lirong L Feng Huanqing H

Bioinformation 20080411 7

Gene selection is to detect the most significantly expressed genes under different conditions expression data. The current challenge in gene selection is the comparison of a large number of genes with limited patient samples. Thus it is trivial task in simple statistical analysis. Various statistical measurements are adopted by filter methods applied in gene selection studies. Their ability to discriminate phenotypes is crucial in classification and selection. Here we describe the standard devia ...[more]

PMID: 18478083

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Project description:BackgroundAmong the primary goals of microarray analysis is the identification of genes that could distinguish between different phenotypes (feature selection). Previous studies indicate that incorporating prior information of the genes' function could help identify physiologically relevant features. However, current methods that incorporate prior functional information do not provide a relative estimate of the effect of different genes on the biological processes of interest.ResultsHere, we present a method that integrates gene ontology (GO) information and expression data using Bayesian regression mixture models to perform unsupervised clustering of the samples and identify physiologically relevant discriminating features. As a model application, the method was applied to identify the genes that play a role in the cytotoxic responses of human hepatoblastoma cell line (HepG2) to saturated fatty acid (SFA) and tumor necrosis factor (TNF)-alpha, as compared to the non-toxic response to the unsaturated FFAs (UFA) and TNF-alpha. Incorporation of prior knowledge led to a better discrimination of the toxic phenotypes from the others. The model identified roles of lysosomal ATPases and adenylate cyclase (AC9) in the toxicity of palmitate. To validate the role of AC in palmitate-treated cells, we measured the intracellular levels of cyclic AMP (cAMP). The cAMP levels were found to be significantly reduced by palmitate treatment and not by the other FFAs, in accordance with the model selection of AC9.ConclusionsA framework is presented that incorporates prior ontology information, which helped to (a) perform unsupervised clustering of the phenotypes, and (b) identify the genes relevant to each cluster of phenotypes. We demonstrate the proposed framework by applying it to identify physiologically-relevant feature genes that conferred differential toxicity to saturated vs. unsaturated FFAs. The framework can be applied to other problems to efficiently integrate ontology information and expression data in order to identify feature genes.

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Dataset Information

SDED: a novel filter method for cancer-related gene selection.

Publications

SDED: a novel filter method for cancer-related gene selection.

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