To 5D and beyond: Quantitative fluorescence microscopy in the postgenomic era

被引:47
作者
Andrews, PD
Harper, IS
Swedlow, JR
机构
[1] Univ Dundee, Div Gene Regulat & Express, Dundee DD1 5EH, Scotland
[2] Monash Univ, Clayton, Vic 3800, Australia
关键词
confocal microscopy; deconvolution; microscopy; restoration; three-dimensional imaging;
D O I
10.1034/j.1600-0854.2002.30105.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Digital fluorescence microscopy is now a standard technology for assaying molecular localisation in cells and tissues. The choice of laser scanning (LSM) and wide-field microscopes (WFM) largely depends on the type of sample, with LSMs performing best on thick samples and WFMs performing best on thin ones. These systems are increasingly used to collect large multidimensional datasets. We propose a unified image structure that considers space, time, and fluorescence wavelength as integral parts of the image. Moreover, the application of fluorescence imaging to large-scale screening means that large datasets are now routinely acquired. We propose that analysis of these data requires querying tools based on relational databases and describe one such system.
引用
收藏
页码:29 / 36
页数:8
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