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

机译:利用墙壁大小的高分辨率显示拷贝数变异的比较基因组学分析

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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 10x 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经常在传统(桌面)显示上的当前数据可视化方法。本文介绍了两种类型的解决方案,利用墙壁大小的高分辨率显示器(师范定值),其具有比桌面显示器更高的显示房地产(即像素)的数量级。首先允许用户查看现有软件输出的副本数变型(CNV)的详细图形。令人逆境的分辨率允许用户在视觉上分析的生物信息学输出的粒度增加10倍,这揭示了先前已从底层数据中平滑的模式。第二个涉及的交互式可视化软件是创新的,因为它使用音乐分数隐喻来铺设CNV数据,克服了由放大/删除阈值引起的感知失真,使用过滤以减少图形数据过载,并且是第一个比较基因组学可视化软件旨在利用令人尴尬的房地产。在场地评估中,临床用户在处理其数据的处理方式中发现了基本误差,并通过使用它在丙型肝炎肝细胞癌中的已知遗传模式“找到”已知的遗传模式来确定对软件的信心。

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