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Cytology Microarrays

The use of high throughput genetic and expression platforms are generating many candidate diagnostic markers and therapeutic targets for a wide variety of clinical conditions. Tissue microarrays can be used for the evaluation of the utility of many of these markers. However, tissue microarrays can s...

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Detalles Bibliográficos
Autores principales: Korbelik, J., Cardeno, M., Matisic, J. P., Carraro, A. C., MacAulay, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618017/
https://www.ncbi.nlm.nih.gov/pubmed/17726265
http://dx.doi.org/10.1155/2007/258297
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author Korbelik, J.
Cardeno, M.
Matisic, J. P.
Carraro, A. C.
MacAulay, C.
author_facet Korbelik, J.
Cardeno, M.
Matisic, J. P.
Carraro, A. C.
MacAulay, C.
author_sort Korbelik, J.
collection PubMed
description The use of high throughput genetic and expression platforms are generating many candidate diagnostic markers and therapeutic targets for a wide variety of clinical conditions. Tissue microarrays can be used for the evaluation of the utility of many of these markers. However, tissue microarrays can suffer from the limitations associated with sampling and sectioning tissues. We introduce a novel microarray technique based on cell suspensions. Multiple slides can be made, all of which are equally representative of the initial sample. A robotic device was designed that can deposit 60 distinct spots of cytological material on a glass slide. Each spot of cells deposited in this manner may correspond to a unique source. Controlling the number of cells per spot, their distribution within the spot and the size of the spot can be achieved by modifying the viscosity of the cell solution or regulating the amount of fluid deposited. A fully automated analysis of quantitatively stained microarray samples has been performed to quantify the number of cells per spot, the size of spots and the DNA amount per cell in each spot. The reproducibility of these parameters was found to be high.
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spelling pubmed-46180172016-01-12 Cytology Microarrays Korbelik, J. Cardeno, M. Matisic, J. P. Carraro, A. C. MacAulay, C. Cell Oncol Other The use of high throughput genetic and expression platforms are generating many candidate diagnostic markers and therapeutic targets for a wide variety of clinical conditions. Tissue microarrays can be used for the evaluation of the utility of many of these markers. However, tissue microarrays can suffer from the limitations associated with sampling and sectioning tissues. We introduce a novel microarray technique based on cell suspensions. Multiple slides can be made, all of which are equally representative of the initial sample. A robotic device was designed that can deposit 60 distinct spots of cytological material on a glass slide. Each spot of cells deposited in this manner may correspond to a unique source. Controlling the number of cells per spot, their distribution within the spot and the size of the spot can be achieved by modifying the viscosity of the cell solution or regulating the amount of fluid deposited. A fully automated analysis of quantitatively stained microarray samples has been performed to quantify the number of cells per spot, the size of spots and the DNA amount per cell in each spot. The reproducibility of these parameters was found to be high. IOS Press 2007 2007-08-13 /pmc/articles/PMC4618017/ /pubmed/17726265 http://dx.doi.org/10.1155/2007/258297 Text en Copyright © 2007 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Korbelik, J.
Cardeno, M.
Matisic, J. P.
Carraro, A. C.
MacAulay, C.
Cytology Microarrays
title Cytology Microarrays
title_full Cytology Microarrays
title_fullStr Cytology Microarrays
title_full_unstemmed Cytology Microarrays
title_short Cytology Microarrays
title_sort cytology microarrays
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618017/
https://www.ncbi.nlm.nih.gov/pubmed/17726265
http://dx.doi.org/10.1155/2007/258297
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