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Analysis of boutique arrays: A universal method for the selection of the optimal data normalization procedure

机译:精品阵列分析:选择最佳数据标准化程序的通用方法

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摘要

DNA microarrays, which are among the most popular genomic tools, are widely applied in biology and medicine. Boutique arrays, which are small, spotted, dedicated microarrays, constitute an inexpensive alternative to whole-genome screening methods. The data extracted from each microarray-based experiment must be transformed and processed prior to further analysis to eliminate any technical bias. The normalization of the data is the most crucial step of microarray data pre-processing and this process must be carefully considered as it has a profound effect on the results of the analysis. Several normalization algorithms have been developed and implemented in data analysis software packages. However, most of these methods were designed for whole-genome analysis. In this study, we tested 13 normalization strategies (ten for double-channel data and three for single-channel data) available on R Bioconductor and compared their effectiveness in the normalization of four boutique array datasets. The results revealed that boutique arrays can be successfully normalized using standard methods, but not every method is suitable for each dataset. We also suggest a universal seven-step workflow that can be applied for the selection of the optimal normalization procedure for any boutique array dataset. The described workflow enables the evaluation of the investigated normalization methods based on the bias and variance values for the control probes, a differential expression analysis and a receiver operating characteristic curve analysis. The analysis of each component results in a separate ranking of the normalization methods. A combination of the ranks obtained from all the normalization procedures facilitates the selection of the most appropriate normalization method for the studied dataset and determines which methods can be used interchangeably.
机译:DNA芯片是最流行的基因组工具之一,已广泛应用于生物学和医学领域。小型,斑点,专用微阵列的精品阵列构成了全基因组筛选方法的廉价替代品。从每个基于微阵列的实验中提取的数据必须先进行转换和处理,然后再进行进一步分析,以消除任何技术偏见。数据的规范化是微阵列数据预处理的最关键步骤,必须仔细考虑此过程,因为它对分析结果有深远影响。在数据分析软件包中已经开发并实现了几种归一化算法。但是,大多数这些方法都是为全基因组分析而设计的。在这项研究中,我们测试了R Bioconductor上可用的13种归一化策略(十个用于双通道数据,三个用于单通道数据),并比较了它们在四个精品阵列数据集归一化中的有效性。结果表明,精品阵列可以使用标准方法成功归一化,但并非每种方法都适用于每个数据集。我们还建议了一个通用的七步工作流,该工作流可用于选择任何精品阵列数据集的最佳归一化过程。所描述的工作流程能够基于对照探针的偏差和方差值,差异表达分析和接收器工作特性曲线分析,对所研究的归一化方法进行评估。对每个组件的分析都会对归一化方法进行单独排名。从所有规范化过程中获得的等级组合有助于为研究的数据集选择最合适的规范化方法,并确定哪些方法可以互换使用。

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