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Structured polychotomous machine diagnosis of multiple cancer types using gene expression

机译:利用基因表达对多种类型的癌症进行结构化多发机器诊断

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Motivation: The problem of class prediction has received a tremendous amount of attention in the literature recently. In the context of DNA microarrays, where the task is to classify and predict the diagnostic category of a sample on the basis of its gene expression profile, a problem of particular importance is the diagnosis of cancer type based on microarray data. One method of classification which has been very successful in cancer diagnosis is the support vector machine (SVM). The latter has been shown (through simulations) to be superior in comparison with other methods, such as classical discriminant analysis, however, SVM suffers from the drawback that the solution is implicit and therefore is difficult to interpret. In order to remedy this difficulty, an analysis of variance decomposition using structured kernels is proposed and is referred to as the structured polychotomous machine. This technique utilizes Newton-Raphson to find estimates of coefficients followed by the Rao and Wald tests, respectively, for addition and deletion of import vectors.
机译:动机:班级预测问题最近在文献中引起了广泛关注。在DNA微阵列的背景下,任务是根据其基因表达谱对样品的诊断类别进行分类和预测,特别重要的问题是基于微阵列数据的癌症类型诊断。在癌症诊断中非常成功的一种分类方法是支持向量机(SVM)。与其他方法(例如经典判别分析)相比,后者(通过仿真)已显示出优越的性能,但是SVM的缺点是解决方案是隐式的,因此难以解释。为了解决该困难,提出了使用结构化内核的方差分解分析,并将其称为结构化多切分机。该技术利用牛顿-拉夫森(Newton-Raphson)查找系数的估计值,然后分别进行Rao和Wald检验,以增加和删除输入向量。

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