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Pathway-based visualization of cross-platform microarray datasets

机译:跨平台微阵列数据集基于路径的可视化

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Motivation: Traditionally, microarrays were almost exclusively used for the genome-wide analysis of differential gene expression. But nowadays, their scope of application has been extended to various genomic features, such as microRNAs (miRNAs), proteins and DNA methylation (DNAm). Most available methods for the visualization of these datasets are focused on individual platforms and are not capable of integratively visualizing multiple microarray datasets from cross-platform studies. Above all, there is a demand for methods that can visualize genomic features that are not directly linked to protein-coding genes, such as regulatory RNAs (e.g. miRNAs) and epigenetic alterations (e.g. DNAm), in a pathway-centred manner. Results: We present a novel pathway-based visualization method that is especially suitable for the visualization of high-throughput datasets from multiple different microarray platforms that were used for the analysis of diverse genomic features in the same set of biological samples. The proposed methodology includes concepts for linking DNAm and miRNA expression datasets to canonical signalling and metabolic pathways. We further point out strategies for displaying data from multiple proteins and protein modifications corresponding to the same gene. Ultimately, we show how data from four distinct platform types (messenger RNA, miRNA, protein and DNAm arrays) can be integratively visualized in the context of canonical pathways.
机译:动机:传统上,微阵列几乎专门用于全基因组差异基因表达的分析。但是如今,它们的应用范围已扩展到各种基因组特征,例如microRNA(miRNA),蛋白质和DNA甲基化(DNAm)。用于可视化这些数据集的大多数可用方法都集中在单个平台上,并且不能从多个跨平台研究中整体可视化多个微阵列数据集。最重要的是,需要一种以途径为中心的方法来可视化与蛋白质编码基因不直接相关的基因组特征,例如调节RNA(例如miRNA)和表观遗传改变(例如DNAm)。结果:我们提出了一种基于途径的新型可视化方法,该方法特别适用于可视化来自多个不同微阵列平台的高通量数据集,这些数据用于分析同一组生物样品中各种基因组特征。拟议的方法包括将DNAm和miRNA表达数据集链接到规范信号和代谢途径的概念。我们进一步指出了显示来自多个蛋白质的数据以及对应于同一基因的蛋白质修饰的策略。最终,我们展示了如何在规范途径的背景下对来自四种不同平台类型(信使RNA,miRNA,蛋白质和DNAm阵列)的数据进行整合可视化。

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