Real-time True-color Volume Visualization of Multi-channel 3D CLSM Images Based on CUDA

被引:0
作者
Dai, Yakang [1 ]
Zhang, Yunhai [1 ]
Zhou, Zhiyong [1 ]
Yang, Haomin [1 ]
Xue, Xiaojun [1 ]
机构
[1] Chinese Acad Sci, Suzhou Inst Biomed Engn & Technol, Suzhou 215163, Peoples R China
来源
PROCEEDINGS IWBBIO 2014: INTERNATIONAL WORK-CONFERENCE ON BIOINFORMATICS AND BIOMEDICAL ENGINEERING, VOLS 1 AND 2 | 2014年
关键词
CLSM; multi-channel 3D images; visualization; volume rendering; CUDA; CONFOCAL MICROSCOPY; FLUORESCENCE;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Confocal laser scanning microscope (CLSM) can obtain multi-channel 3D images from biological tissues for analysis of tissue structures, where each channel results from a particular fluorescent label. The visualization of the multi-channel 3D confocal microscope images is required for qualitative, interactive, and even quantitative analysis of the structures of the studied tissues. Despite the available volume rendering algorithms for visualization of single-channel 3D images, the algorithms and toolkits specially used for true-color volume visualization of multi-channel 3D confocal microscope images were seldom reported. We have developed a new true-color volume rendering tool for real-time volume visualization of the multi-channel 3D confocal microscope images based on compute unified device architecture (CUDA). Manipulations including rotation, translation, and zooming are integrated with the volume rendering for interactive analysis of the multi-channel 3D images. In this paper, the methodologies of the tool are described and experimental results are illustrated. The tool is free of charge for research purpose.
引用
收藏
页码:1686 / 1693
页数:8
相关论文
共 17 条
  • [1] Stimulated emission depletion microscopy with a supercontinuum source and fluorescence lifetime imaging
    Auksorius, Egidijus
    Boruah, Bosanta R.
    Dunsby, Christopher
    Lanigan, Peter M. P.
    Kennedy, Gordon
    Neil, Mark A. A.
    French, Paul M. W.
    [J]. OPTICS LETTERS, 2008, 33 (02) : 113 - 115
  • [2] Lateral resolution enhancement in confocal microscopy by vectorial aperture engineering
    Boruah, B. R.
    [J]. APPLIED OPTICS, 2010, 49 (04) : 701 - 707
  • [3] Simultaneous multi-lifetime multi-color STED imaging for colocalization analyses
    Bueckers, Johanna
    Wildanger, Dominik
    Vicidomini, Giuseppe
    Kastrup, Lars
    Hell, Stefan W.
    [J]. OPTICS EXPRESS, 2011, 19 (04): : 3130 - 3143
  • [4] Voxx: a PC-based, near real-time volume rendering system for biological microscopy
    Clendenon, JL
    Phillips, CL
    Sandoval, RM
    Fang, SF
    Dunn, KW
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 282 (01): : C213 - C218
  • [5] Dobbs J.L., 2012, BIOM OPT OSA OPT SOC
  • [6] Hibbs A.R., 2004, CONFOCAL MICROSCOPY
  • [7] Characterizing image quality in a scanning laser ophthalmoscope with differing pinholes and induced scattered light
    Hunter, Jennifer J.
    Cookson, Christopher J.
    Kisilak, Marsha L.
    Bueno, Juan M.
    Campbell, Melanie C. W.
    [J]. JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 2007, 24 (05) : 1284 - 1295
  • [8] Single-molecule detection of fluorescence resonance energy transfer using confocal microscopy
    Kim, Sung Hyun
    Choi, Don Seong
    Kim, Doseok
    [J]. JOURNAL OF THE OPTICAL SOCIETY OF KOREA, 2008, 12 (02) : 107 - 111
  • [9] Matsumoto B., 2002, METHODS CELL BIOL, V70
  • [10] Role of three-dimensional bleach distribution in confocal and two-photon fluorescence recovery after photobleaching experiments
    Mazza, Davide
    Cella, Francesca
    Vicidomini, Giuseppe
    Krol, Silke
    Diaspro, Alberto
    [J]. APPLIED OPTICS, 2007, 46 (30) : 7401 - 7411