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An Incremental Linear Programming Based Tool for Analyzing Gene Expression Data

机译:基于基于基于基于基于基于基于基于基因表达数据的基于程序的工具

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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已经为基于基因表达分析的各种疾病的诊断和治疗开辟了新的门。在本文中,我们讨论了基于线性编程的新型分析工具。给定来自同一疾病的两个亚类(例如白血病)的基因表达数据,如果样品相对于基因三胞胎线性可分离,我们能够有效地确定。在早期的研究中,这被留下了一个公开问题,认为仅被视为线性分离器的一对基因。我们的工具有两个版本 - 离线和增量。测试表明增量版本明显比离线更有效。本文还介绍了一种基因选择策略,通过对和三胞胎通过可分离试验利用基因的类别分化性能。我们将基因选择策略应用于4个公开的基因表达数据集。我们的实验表明,我们的方法产生的基因空间比T值,FCS(FISHERION评分)和SAM(微射线意义分析)实现了比基因空间相似或更好的分类精度。

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