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Missing Value Imputation Framework for Microarray Significant Gene Selection and Class Prediction

机译:用于微阵列显着基因选择和课程预测的缺失价值估算框架

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Microarray data is used in a large number of applications ranging from diagnosis through to drug discovery. Such data however, often contains multiple missing genetic expressions which are generally ignored thus degrading the reliability of inferred results. This paper presents an innovative and robust imputation framework that more accurately estimates missing values leading subsequently to better gene selection and class prediction. To prove this premise, several missing value techniques including the Collateral Missing Values Estimation (CMVE), Bayesian Principal Component Analysis (BPCA), Least Square Impute (LSImpute), k-Nearest Neighbour (KNN) and ZeroImpute are analysed. A combination of univariate and multiple gene selection methods, namely, Between Group to within Group Sum of Squares and Weighted Partial Least Squares is then performed before applying class prediction using the Ridge Partial Least Square method. Overall, CMVE imputation consistently provided superior missing values estimation accuracy compared with the other algorithms examined, by virtue of exploiting local and global as well as positive and negative correlations between genes, with all empirical results being corroborated by the two-sided Wilcoxon Rank sum statistical significance test.
机译:微阵列数据用于大量应用范围,从诊断到药物发现。然而,这种数据通常包含多个缺失的遗传表达,这通常被忽略,从而降低推断结果的可靠性。本文介绍了一种创新和强大的借调框架,更准确地估计缺失值,随后以更好的基因选择和课堂预测。为了证明这一点的前提下,几个缺失值技术,包括担保品的缺失值估计(CMVE),贝叶斯主成分分析(BPCA),最小二乘推诿(LSImpute),k近邻(KNN)和ZeroImpute进行了分析。然后在使用脊部分最小二乘法的应用程序预测之前进行单变量和多种基因选择方法的组合,即组到组的正方形和加权部分最小二乘之间。总体而言,与在基因之间的局部和全球范围内的其他算法相比,CMVE载升始终提供优异的缺失值估计准确度,并通过基因之间的阳性和阳性和负相关性,所有经验结果被双面Wilcoxon等级总和统计所证实意义测试。

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