FluoRender: An Application of 2D Image Space Methods for 3D and 4D Confocal Microscopy Data Visualization in Neurobiology Research.

Yong Wan, Hideo Otsuna, Chi-Bin Chien, Charles Hansen
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Abstract

2D image space methods are processing methods applied after the volumetric data are projected and rendered into the 2D image space, such as 2D filtering, tone mapping and compositing. In the application domain of volume visualization, most 2D image space methods can be carried out more efficiently than their 3D counterparts. Most importantly, 2D image space methods can be used to enhance volume visualization quality when applied together with volume rendering methods. In this paper, we present and discuss the applications of a series of 2D image space methods as enhancements to confocal microscopy visualizations, including 2D tone mapping, 2D compositing, and 2D color mapping. These methods are easily integrated with our existing confocal visualization tool, FluoRender, and the outcome is a full-featured visualization system that meets neurobiologists' demands for qualitative analysis of confocal microscopy data.

FluoRender:神经生物学研究中三维和四维共聚焦显微镜数据可视化的二维图像空间方法应用。
二维图像空间方法是在将体积数据投影和渲染到二维图像空间后应用的处理方法,如二维滤波、色调映射和合成。在体积可视化应用领域,大多数二维图像空间方法都能比其三维对应方法更有效地执行。最重要的是,当二维图像空间方法与体积渲染方法一起应用时,可用于提高体积可视化质量。在本文中,我们介绍并讨论了一系列二维图像空间方法在共聚焦显微可视化中的应用,包括二维色调映射、二维合成和二维色彩映射。这些方法很容易与我们现有的共聚焦可视化工具 FluoRender 相集成,从而形成一个功能齐全的可视化系统,满足神经生物学家对共聚焦显微镜数据进行定性分析的需求。
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