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Methodological study of affine transformations of gene expression data with proposed robust non-parametric multi-dimensional normalization method

机译:拟议的鲁棒非参数多维归一化方法对基因表达数据进行仿射变换的方法学研究

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Background Low-level processing and normalization of microarray data are most important steps in microarray analysis, which have profound impact on downstream analysis. Multiple methods have been suggested to date, but it is not clear which is the best. It is therefore important to further study the different normalization methods in detail and the nature of microarray data in general. Results A methodological study of affine models for gene expression data is carried out. Focus is on two-channel comparative studies, but the findings generalize also to single- and multi-channel data. The discussion applies to spotted as well as in-situ synthesized microarray data. Existing normalization methods such as curve-fit ("lowess") normalization, parallel and perpendicular translation normalization, and quantile normalization, but also dye-swap normalization are revisited in the light of the affine model and their strengths and weaknesses are investigated in this context. As a direct result from this study, we propose a robust non-parametric multi-dimensional affine normalization method, which can be applied to any number of microarrays with any number of channels either individually or all at once. A high-quality cDNA microarray data set with spike-in controls is used to demonstrate the power of the affine model and the proposed normalization method. Conclusion We find that an affine model can explain non-linear intensity-dependent systematic effects in observed log-ratios. Affine normalization removes such artifacts for non-differentially expressed genes and assures that symmetry between negative and positive log-ratios is obtained, which is fundamental when identifying differentially expressed genes. In addition, affine normalization makes the empirical distributions in different channels more equal, which is the purpose of quantile normalization, and may also explain why dye-swap normalization works or fails. All methods are made available in the aroma package, which is a platform-independent package for R.
机译:背景技术微阵列数据的低级处理和规范化是微阵列分析中最重要的步骤,对下游分析产生深远影响。迄今为止,已经提出了多种方法,但是尚不清楚哪种方法最好。因此,重要的是进一步详细研究不同的归一化方法以及总体上微阵列数据的性质。结果进行了仿射模型基因表达数据的方法学研究。重点是两通道比较研究,但研究结果也推广到单通道和多通道数据。该讨论适用于斑点以及原位合成的微阵列数据。根据仿射模型重新研究了现有的归一化方法,例如曲线拟合(“ lowess”)归一化,平行和垂直平移归一化以及分位数归一化,以及染料交换归一化,并在此背景下研究了它们的优缺点。 。作为这项研究的直接结果,我们提出了一种鲁棒的非参数多维仿射归一化方法,该方法可以应用于具有任意数量通道的任意数量的微阵列,无论是单个通道还是全部通道。具有尖峰插入控件的高质量cDNA微阵列数据集用于证明仿射模型和拟议的归一化方法的功能。结论我们发现仿射模型可以解释观测到的对数比中非线性强度依赖的系统效应。仿射归一化消除了非差异表达基因的这种伪像,并确保获得了负对数正比对数的对称性,这在鉴定差异表达基因时至关重要。此外,仿射归一化使不同通道中的经验分布更加均等,这是分位数归一化的目的,并且还可以解释为什么染料交换归一化有效或失败。所有方法都在aroma软件包中提供,该软件包是R的与平台无关的软件包。

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