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Pathway-BasedFeature Selection Algorithm for Cancer Microarray Data

机译:基于路径的癌症微阵列数据特征选择算法

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摘要

Classification of cancers based on gene expressions produces better accuracywhen compared to that of the clinical markers. Feature selection improvesthe accuracy of these classification algorithms by reducing the chanceof overfitting that happens due to large number of features. We develop anew feature selection method called Biological Pathway-based Feature Selection (BPFS) for microarray data. Unlike most of the existing methods,our method integrates signaling and gene regulatory pathways with geneexpression data to minimize the chance of overfitting of the method and toimprove the test accuracy. Thus, BPFS selects a biologically meaningful featureset that is minimally redundant. Our experiments on published breastcancer datasets demonstrate that all of the top 20 genes found by our methodare associated with cancer. Furthermore, the classification accuracy of oursignature is up to 18% better than that of vant Veers 70 gene signature,and it is up to 8% better accuracy than the best published feature selectionmethod, I-RELIEF.
机译:与临床标记相比,基于基因表达的癌症分类产生更高的准确性。特征选择通过减少由于大量特征而发生过度拟合的机会来提高这些分类算法的准确性。我们为微阵列数据开发了一种新的特征选择方法,称为基于生物途径的特征选择(BPFS)。与大多数现有方法不同,我们的方法将信号传导和基因调控途径与基因表达数据集成在一起,以最大程度地降低该方法过拟合的机会并提高测试准确性。因此,BPFS选择具有最小冗余的生物学意义的特征集。我们在已发布的乳腺癌数据集上进行的实验表明,我们的方法发现的所有前20个基因均与癌症有关。此外,我们的签名的分类准确度比vant Veers 70基因签名提高了18%,比最佳发表的特征选择方法I-RELIEF高8%。

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