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多通道体数据的三维可视化:amSFP算法

Three-dimensional visualization of multi-channel volume data: the amSFP algorithm.

作者信息

Messerli J M, van der Voort H T, Rungger-Brändle E, Perriard J C

机构信息

Institute for Cell Biology, Swiss Federal Institute of Technology, Zurich.

出版信息

Cytometry. 1993 Oct;14(7):725-35. doi: 10.1002/cyto.990140705.

Abstract

In this paper we present a three-dimensional visualization technique for multi-channel volume data. The technique simulates the physical process of fluorescence, hence its name: achromatic multi-channel simulated fluorescent process (amSFP). The data set is simulated as 3D distribution of different fluorescent dyes, where each channel is represented by a particular type of dye. Apart from the spatial density map, no additional characteristics about the data set have to be defined; no image segmentation is needed prior to visualization. The degree of interaction among the channels in the fluorescence process can be adapted to optimally render specific structures in the image. 3D multi-channel data can be obtained by a three-dimensional imaging device that is able to measure a number of physical quantities at a given location within a specimen. The fluorescence principle, the algorithm, and its implementation are presented. We have used the technique to investigate the relative spatial arrangement of blood vessels and astrocytes in the cat retina. The two components have been stained with different fluorescence dyes and recorded in a confocal light microscope to form a two-channel 3D data set.

摘要

在本文中,我们提出了一种用于多通道体数据的三维可视化技术。该技术模拟了荧光的物理过程,因此其名称为:消色差多通道模拟荧光过程(amSFP)。数据集被模拟为不同荧光染料的三维分布,其中每个通道由特定类型的染料表示。除了空间密度图外,无需定义关于数据集的其他特征;在可视化之前不需要图像分割。荧光过程中通道之间的相互作用程度可以进行调整,以最佳地呈现图像中的特定结构。三维多通道数据可以通过三维成像设备获得,该设备能够在标本内的给定位置测量多个物理量。本文介绍了荧光原理、算法及其实现。我们已经使用该技术研究了猫视网膜中血管和星形胶质细胞的相对空间排列。这两个成分用不同的荧光染料进行了染色,并在共聚焦光学显微镜中进行记录,以形成一个双通道三维数据集。

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