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

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About: Automated confocal microscopy: The way of achieving both quality and quantity in 3D image cytometry Goto Sponge NotDistinct Permalink

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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. 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. (en)
Title	Automated confocal microscopy: The way of achieving both quality and quantity in 3D image cytometry Automated confocal microscopy: The way of achieving both quality and quantity in 3D image cytometry (en)
skos:prefLabel	Automated confocal microscopy: The way of achieving both quality and quantity in 3D image cytometry Automated confocal microscopy: The way of achieving both quality and quantity in 3D image cytometry (en)
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http://linked.open...vai/riv/dodaniDat	2011
http://linked.open...aciTvurceVysledku	Kozubek, Michal Matula, Pavel Matula, Petr
http://linked.open.../riv/druhVysledku	D - Článek ve sborníku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Masarykova univerzita / Fakulta informatiky
http://linked.open...dnocenehoVysledku	555646
http://linked.open...ai/riv/idVysledku	RIV/00216224:14330/04:00009713
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	image cytometry; confocal microscopy (en)
http://linked.open.../riv/klicoveSlovo	confocal microscopy image cytometry
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http://linked.open...v/mistoKonaniAkce	Arlington, USA
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http://linked.open...i/riv/nazevZdroje	International Symposium on Biomedical Imaging
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http://linked.open...vavai/riv/projekt	Human genome structure Development of new diagnostic techniques for oncology
http://linked.open...UplatneniVysledku	2004
http://linked.open...iv/tvurceVysledku	Matula, Pavel Kozubek, Michal Matula, Petr
http://linked.open...vavai/riv/typAkce	WRD - Světová
http://linked.open.../riv/zahajeniAkce	2004-04-15 (xsd:date)
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number of pages	4 (xsd:int)
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