DEVELOPMENT OF A SEMI-AUTOMATIC ALGORITHM FOR DECONVOLUTION AND QUANTIFICATION OF THREE-DIMENSIONAL MICROSCOPY IMAGES

被引:0
|
作者
Vicente, N. B. [1 ]
Diaz-Zamboni, J. E. [1 ]
Adur, J. F. [1 ]
Izaguirre, M. F. [1 ]
Galetto, C. D. [1 ]
Casco, V. H. [1 ]
机构
[1] UNER, Fac Ingn, Lab Microscopia Aplicada Estudios Mol & Celulares, RA-3101 Oro Verde, Entre Rios, Argentina
来源
ACTA MICROSCOPICA | 2010年 / 19卷 / 03期
关键词
Automatic algorithm; deconvolution; quantification; microscopy; multidimensional images; FLUORESCENCE MICROSCOPY; CELL-ADHESION; E-CADHERIN;
D O I
暂无
中图分类号
TH742 [显微镜];
学科分类号
摘要
Modern microscopy enables the acquisition of massive volumes of information. Processing and evaluating large multidimensional images is time-consuming, especially when working with various stacks. In the present work we have developed a software tool for the optimization of image processing, which consists of an automatic deconvolution and quantification algorithm that eliminates non-systematic errors and significantly decreases processing time. This tool included a restoration deconvolution method (positive constrained algorithm) and five image-restoration parameters (Contrast-to-Noise Ratio, Signal-to-Noise Ratio, Full-Width at Half-Maximum and two three-dimensional Tenengrad-based indicators) used to assess quantitatively the quality of restoration. This algorithm was used to process raw three-dimensional images using several experimental Point Spread Functions; raw images were obtained by fluorescence wide-field microscopy of epidermal E-cadherin expression in Rhinella (= Bufo) arenarum embryos and fluorescent microspheres. The image-restoration indicators and the performance of the algorithm were evaluated. Results show that all indicators concur and do not increase processing time significantly, constituting a valuable tool for 3D microscopy analysis.
引用
收藏
页码:328 / 336
页数:9
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