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An Incremental Linear Programming Based Tool for Analyzing Gene Expression Data

机译:基于增量线性规划的基因表达数据分析工具

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The availability of large volumes of gene expression data from microarray analysis (cDNA and oligonucleotide) has opened a new door to the diagnoses and treatments of various diseases based on gene expression profiling. In this paper, we discuss a new profiling tool based on linear programming. Given gene expression data from two subclasses of the same disease (e.g. leukemia), we are able to determine efficiently if the samples are linearly separable with respect to triplets of genes. This was left as an open problem in an earlier study that considered only pairs of genes as linear separators. Our tool comes in two versions - offline and incremental. Tests show that the incremental version is markedly more efficient than the offline one. This paper also introduces a gene selection strategy that exploits the class distinction property of a gene by separability test by pairs and triplets. We applied our gene selection strategy to 4 publicly available gene-expression data sets. Our experiments show that gene spaces generated by our method achieves similar or even better classification accuracy than the gene spaces generated by t-values, FCS(Fisher Criterion Score) and SAM(Significance Analysis of Microar-rays).
机译:来自微阵列分析(cDNA和寡核苷酸)的大量基因表达数据的可用性为基于基因表达谱分析的各种疾病的诊断和治疗打开了新的大门。在本文中,我们讨论了一种基于线性编程的新性能分析工具。给定来自同一疾病(例如白血病)的两个亚类的基因表达数据,我们能够有效地确定样本相对于三胞胎基因是否可线性分离。在早期的研究中,仅将成对的基因视为线性分隔符,这是一个悬而未决的问题。我们的工具有两个版本-离线版本和增量版本。测试表明,增量版本明显比脱机版本有效。本文还介绍了一种基因选择策略,该策略通过通过成对和三联体的可分离性测试来利用基因的类别区分特性。我们将我们的基因选择策略应用于4个公开可用的基因表达数据集。我们的实验表明,与t值,FCS(Fisher Criterion Score)和SAM(Microar-rays的显着性分析)所产生的基因空间相比,我们的方法所产生的基因空间具有相似甚至更好的分类精度。

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