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A Review of Pathway-Based Analysis Tools That Visualize Genetic Variants

机译:可视化遗传变异的基于途径的分析工具综述

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摘要

Pathway analysis is a powerful method for data analysis in genomics, most often applied to gene expression analysis. It is also promising for single-nucleotide polymorphism (SNP) data analysis, such as genome-wide association study data, because it allows the interpretation of variants with respect to the biological processes in which the affected genes and proteins are involved. Such analyses support an interactive evaluation of the possible effects of variations on function, regulation or interaction of gene products. Current pathway analysis software often does not support data visualization of variants in pathways as an alternate method to interpret genetic association results, and specific statistical methods for pathway analysis of SNP data are not combined with these visualization features. In this review, we first describe the visualization options of the tools that were identified by a literature review, in order to provide insight for improvements in this developing field. Tool evaluation was performed using a computational epistatic dataset of gene–gene interactions for obesity risk. Next, we report the necessity to include in these tools statistical methods designed for the pathway-based analysis with SNP data, expressly aiming to define features for more comprehensive pathway-based analysis tools. We conclude by recognizing that pathway analysis of genetic variations data requires a sophisticated combination of the most useful and informative visual aspects of the various tools evaluated.
机译:途径分析是基因组数据分析的强大方法,通常用于基因表达分析。它也有望用于单核苷酸多态性(SNP)数据分析,例如全基因组关联研究数据,因为它可以解释涉及受影响的基因和蛋白质的生物学过程的变体。此类分析支持对变异对基因产物的功能,调控或相互作用的可能影响进行交互式评估。当前的途径分析软件通常不支持途径变异的数据可视化,作为解释遗传关联结果的替代方法,并且用于SNP数据途径分析的特定统计方法未与这些可视化功能结合在一起。在这篇综述中,我们首先描述通过文献综述确定的工具的可视化选项,以便为该发展中的领域提供改进的见识。评估工具使用的是肥胖风险的基因-基因相互作用的计算上位数据集。接下来,我们报告有必要在这些工具中包括为使用SNP数据进行基于路径的分析而设计的统计方法,明确旨在为更全面的基于路径的分析工具定义功能。我们的结论是,认识到遗传变异数据的路径分析需要对各种评估工具的最有用和最有用的视觉方面进行复杂的组合。

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