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Leveraging wall-sized high-resolution displays for comparative genomics analyses of copy number variation

机译:利用壁式高分辨率显示器进行比较基因组学分析拷贝数变异

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摘要

The scale of comparative genomics data frequently overwhelms current data visualization methods on conventional (desktop) displays. This paper describes two types of solution that take advantage of wall-sized high-resolution displays (WHirDs), which have orders of magnitude more display real estate (i.e., pixels) than desktop displays. The first allows users to view detailed graphics of copy number variation (CNV) that were output by existing software. A WHirD's resolution allowed a 10× increase in the granularity of bioinformatics output that was feasible for users to visually analyze, and this revealed a pattern that had previously been smoothed out from the underlying data. The second involved interactive visualization software that was innovative because it uses a music score metaphor to lay out CNV data, overcomes a perceptual distortion caused by amplification/deletion thresholds, uses filtering to reduce graphical data overload, and is the first comparative genomics visualization software that is designed to leverage a WHirD's real estate. In a field evaluation, a clinical user discovered a fundamental error in the way their data had been processed, and established confidence in the software by using it to 'find' known genetic patterns in hepatitis C-driven hepatocellular cancer.
机译:比较基因组学数据的规模常常使传统(台式)显示器上的当前数据可视化方法不堪重负。本文介绍了两种类型的解决方案,它们利用了墙尺寸的高分辨率显示器(WHirD),它们的显示空间(即像素)比台式机显示器多了几个数量级。第一个允许用户查看现有软件输出的详细副本数变异(CNV)图形。 WHirD的分辨率使生物信息学输出的粒度增加了10倍,这使用户可以直观地进行分析,这揭示了以前已从基础数据中消除的一种模式。第二个涉及交互式可视化软件,该软件具有创新性,因为它使用乐谱隐喻对CNV数据进行布局,克服了由扩增/缺失阈值引起的感知失真,使用过滤来减少图形数据过载,并且是第一个比较基因组学可视化软件,旨在利用WHirD的房地产。在现场评估中,临床用户发现了数据处理方式中的一个基本错误,并通过使用该软件“查找”丙型肝炎驱动的肝细胞癌的已知遗传模式,建立了对该软件的信心。

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