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首页> 外文期刊>IEEE Transactions on Signal Processing >Identifying Differentially Expressed Genes in Microarray Experiments With Model-Based Variance Estimation
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Identifying Differentially Expressed Genes in Microarray Experiments With Model-Based Variance Estimation

机译:使用基于模型的方差估计识别微阵列实验中的差异表达基因

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摘要

Statistical tests have been employed to identify genes differentially expressed under different conditions using data from microarray experiments. The variance of gene expression levels is often required in various statistical tests; however, due to the small number of replicates, the variance estimated from the sample variance is not accurate, which causes large false positive and negative errors. More accurate and robust variance estimation is thus highly desirable to improve the performance of statistical tests. In this paper, cluster analysis was performed on the microarray data using a model-based clustering method. The variance for each gene was then estimated from cluster variances. Since cluster variances are estimated from multiple genes whose microarray data have similar variance, the proposed estimation method pools the relevant genes together; this effectively increases the number of samples in variance estimation, thereby improving variance estimation. Using simulated data, it is shown that with the novel variance estimation, the performance of the t-test, regularized t-test, and a variant of SAM test, which is called the S-test here, can be improved. Using colon microarray data of Alon et al., it is demonstrated that the proposed method offers better or comparable performance compared with other gene pooling methods. Using the IHF microarray data of Arfin et al., it is shown that the proposed novel variance estimation decreases the significance of those genes having a small fold change but a high significant score assigned by the t-test using the sample variance, which potentially reduces false positive probability.
机译:使用来自微阵列实验的数据,采用统计测试来鉴定在不同条件下差异表达的基因。基因表达水平的差异通常在各种统计测试中都需要;但是,由于重复次数少,从样本方差估计的方差不准确,这会导致较大的假正负误差。因此,非常需要更准确和鲁棒的方差估计来改善统计检验的性能。在本文中,使用基于模型的聚类方法对微阵列数据进行聚类分析。然后根据聚类差异估算每个基因的差异。由于簇变异是从多个基因中估计的,这些基因的微阵列数据具有相似的变异,因此所提出的评估方法将相关基因集中在一起。这有效地增加了方差估计中的样本数量,从而改善了方差估计。使用模拟数据显示,通过新颖的方差估计,可以改善t检验,正则t检验和SAM检验的变体(在此称为S检验)的性能。使用Alon等人的结肠微阵列数据,证明了与其他基因合并方法相比,所提出的方法提供了更好或相当的性能。使用Arfin等人的IHF微阵列数据,表明拟议的新颖方差估计降低了倍数变化小的基因的显着性,而t检验使用样本方差分配的显着性得分较高,这有可能降低误报概率。

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