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Automated microscopy for high-content RNAi screening

Fluorescence microscopy is one of the most powerful tools to investigate complex cellular processes such as cell division, cell motility, or intracellular trafficking. The availability of RNA interference (RNAi) technology and automated microscopy has opened the possibility to perform cellular imagi...

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Detalles Bibliográficos
Autores principales: Conrad, Christian, Gerlich, Daniel W.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828931/
https://www.ncbi.nlm.nih.gov/pubmed/20176920
http://dx.doi.org/10.1083/jcb.200910105
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author Conrad, Christian
Gerlich, Daniel W.
author_facet Conrad, Christian
Gerlich, Daniel W.
author_sort Conrad, Christian
collection PubMed
description Fluorescence microscopy is one of the most powerful tools to investigate complex cellular processes such as cell division, cell motility, or intracellular trafficking. The availability of RNA interference (RNAi) technology and automated microscopy has opened the possibility to perform cellular imaging in functional genomics and other large-scale applications. Although imaging often dramatically increases the content of a screening assay, it poses new challenges to achieve accurate quantitative annotation and therefore needs to be carefully adjusted to the specific needs of individual screening applications. In this review, we discuss principles of assay design, large-scale RNAi, microscope automation, and computational data analysis. We highlight strategies for imaging-based RNAi screening adapted to different library and assay designs.
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spelling pubmed-28289312010-08-22 Automated microscopy for high-content RNAi screening Conrad, Christian Gerlich, Daniel W. J Cell Biol Reviews Fluorescence microscopy is one of the most powerful tools to investigate complex cellular processes such as cell division, cell motility, or intracellular trafficking. The availability of RNA interference (RNAi) technology and automated microscopy has opened the possibility to perform cellular imaging in functional genomics and other large-scale applications. Although imaging often dramatically increases the content of a screening assay, it poses new challenges to achieve accurate quantitative annotation and therefore needs to be carefully adjusted to the specific needs of individual screening applications. In this review, we discuss principles of assay design, large-scale RNAi, microscope automation, and computational data analysis. We highlight strategies for imaging-based RNAi screening adapted to different library and assay designs. The Rockefeller University Press 2010-02-22 /pmc/articles/PMC2828931/ /pubmed/20176920 http://dx.doi.org/10.1083/jcb.200910105 Text en © 2010 Conrad and Gerlich This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Reviews
Conrad, Christian
Gerlich, Daniel W.
Automated microscopy for high-content RNAi screening
title Automated microscopy for high-content RNAi screening
title_full Automated microscopy for high-content RNAi screening
title_fullStr Automated microscopy for high-content RNAi screening
title_full_unstemmed Automated microscopy for high-content RNAi screening
title_short Automated microscopy for high-content RNAi screening
title_sort automated microscopy for high-content rnai screening
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828931/
https://www.ncbi.nlm.nih.gov/pubmed/20176920
http://dx.doi.org/10.1083/jcb.200910105
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