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t-Test at the Probe Level: An Alternative Method to Identify Statistically Significant Genes for Microarray Data

机译:探针水平的t检验:识别微阵列数据统计上重要的基因的另一种方法

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摘要

Microarray data analysis typically consists in identifying a list of differentially expressed genes (DEG), i.e., the genes that are differentially expressed between two experimental conditions. Variance shrinkage methods have been considered a better choice than the standard t-test for selecting the DEG because they correct the dependence of the error with the expression level. This dependence is mainly caused by errors in background correction, which more severely affects genes with low expression values. Here, we propose a new method for identifying the DEG that overcomes this issue and does not require background correction or variance shrinkage. Unlike current methods, our methodology is easy to understand and implement. It consists of applying the standard t-test directly on the normalized intensity data, which is possible because the probe intensity is proportional to the gene expression level and because the t-test is scale- and location-invariant. This methodology considerably improves the sensitivity and robustness of the list of DEG when compared with the t-test applied to preprocessed data and to the most widely used shrinkage methods, Significance Analysis of Microarrays (SAM) and Linear Models for Microarray Data (LIMMA). Our approach is useful especially when the genes of interest have small differences in expression and therefore get ignored by standard variance shrinkage methods.
机译:微阵列数据分析通常在于鉴定差异表达基因(DEG)的列表,即两个实验条件之间差异表达的基因。与选择teg的标准t检验相比,方差收缩法被认为是更好的选择,因为它们可以校正误差与表达水平的相关性。这种依赖性主要是由背景校正中的错误引起的,该错误会更严重地影响具有低表达值的基因。在这里,我们提出了一种新的识别DEG的方法,该方法可以克服此问题,并且不需要背景校正或方差收缩。与当前的方法不同,我们的方法易于理解和实施。它包括直接在标准化强度数据上应用标准t检验,这是可能的,因为探针强度与基因表达水平成正比,并且因为t检验是尺度和位置不变的。与应用于预处理数据和最广泛使用的收缩方法,微阵列的重要性分析(SAM)和微阵列数据的线性模型(LIMMA)的t检验相比,此方法大大提高了DEG列表的敏感性和鲁棒性。我们的方法特别有用,特别是当目标基因的表达差异很小,因此被标准方差收缩方法所忽略时。

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