Automated confocal microscopy: The way of achieving both quality and quantity in 3D image cytometry

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Authors

KOZUBEK Michal MATULA Petr MATULA Pavel

Year of publication 2004
Type Article in Proceedings
Conference International Symposium on Biomedical Imaging
MU Faculty or unit

Faculty of Informatics

Citation
Field Use of computers, robotics and its application
Keywords image cytometry; confocal microscopy
Description Image cytometry is mostly associated with high quality but low quantity, whereas flow cytometry is associated with high quantity but low quality. Achieving both quality and quantity in cytometry is possible in the case of automated confocal microscopy systems. We have shown that the automation of image acquisition and image processing in confocal microscopy is possible for specific tasks such as 2D and 3D FISH imaging. This paper is focused on practical problems and solutions that we have encountered during our research. We believe that our experience might be helpful to all those who decide to automate their light microscopy systems for cell studies, i.e. for image cytometry purposes.
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