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Gene Selection for Diagnosis of Cancer in Microarray Data Using Memetic Algorithm

机译:麦克雷算法诊断微阵列数据癌症的基因选择

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Selecting a small subset of genes that helps to build a good classification model for prediction of disease on the microarray data is a very demanding optimization problem. Genetic algorithm (GA) is a population-based optimization algorithm, which has a lot of applications in the field of molecular biology. But the premature convergence is one of the limitations of GA. Memetic algorithm (MA), an extension of GA, diminishes the possibility of such premature convergence. Microarray technology enables to measure the expression level of thousands of genes to recognize the changes in expression level among different biological states. In this paper, superiority of MA is established over GA, simulated annealing (SA), and tabu search (TS), while selecting the genes in microarray data. Experiments on three well-known data sets, namely DLBCL, leukemia, and prostate cancer, exhibit that MA yields more promising results than classical GA, SA, and TS.
机译:选择一个小基因子集,有助于构建良好的分类模型,以便在微阵列数据上预测疾病是一个非常苛刻的优化问题。 遗传算法(GA)是一种基于人群的优化算法,其在分子生物学领域具有大量应用。 但过早融合是GA的局限之一。 Memetic算法(MA),GA的延伸,减少了这种过早收敛的可能性。 微阵列技术使能测量数千个基因的表达水平,以识别不同生物态之间表达水平的变化。 在本文中,在GA,模拟退火(SA)和禁忌搜索(TS)上建立了MA的优越性,同时在微阵列数据中选择基因。 在三种众所周知的数据集,即DLBCL,白血病和前列腺癌中的实验,展示MA比经典GA,SA和TS更有前景结果。

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