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A high-throughput DNA FISH protocol to visualize genome regions in human cells

Here, we describe an end-to-end high-throughput imaging protocol to visualize genomic loci in cells at high throughput using DNA fluorescence in situ hybridization, automated microscopy, and computational analysis. This is particularly useful for quantifying patterns of heterogeneity in relative gen...

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Autores principales: Finn, Elizabeth H., Misteli, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377592/
https://www.ncbi.nlm.nih.gov/pubmed/34458868
http://dx.doi.org/10.1016/j.xpro.2021.100741
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author Finn, Elizabeth H.
Misteli, Tom
author_facet Finn, Elizabeth H.
Misteli, Tom
author_sort Finn, Elizabeth H.
collection PubMed
description Here, we describe an end-to-end high-throughput imaging protocol to visualize genomic loci in cells at high throughput using DNA fluorescence in situ hybridization, automated microscopy, and computational analysis. This is particularly useful for quantifying patterns of heterogeneity in relative gene positioning or differences within subpopulations of cells. We focus on important experimental design and execution steps in this one-week protocol, suggest ways to ensure and verify data quality, and provide practical solutions to common problems. For complete details on the generation and use of this protocol, please refer to Finn et al. (2019).
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spelling pubmed-83775922021-08-26 A high-throughput DNA FISH protocol to visualize genome regions in human cells Finn, Elizabeth H. Misteli, Tom STAR Protoc Protocol Here, we describe an end-to-end high-throughput imaging protocol to visualize genomic loci in cells at high throughput using DNA fluorescence in situ hybridization, automated microscopy, and computational analysis. This is particularly useful for quantifying patterns of heterogeneity in relative gene positioning or differences within subpopulations of cells. We focus on important experimental design and execution steps in this one-week protocol, suggest ways to ensure and verify data quality, and provide practical solutions to common problems. For complete details on the generation and use of this protocol, please refer to Finn et al. (2019). Elsevier 2021-08-16 /pmc/articles/PMC8377592/ /pubmed/34458868 http://dx.doi.org/10.1016/j.xpro.2021.100741 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Finn, Elizabeth H.
Misteli, Tom
A high-throughput DNA FISH protocol to visualize genome regions in human cells
title A high-throughput DNA FISH protocol to visualize genome regions in human cells
title_full A high-throughput DNA FISH protocol to visualize genome regions in human cells
title_fullStr A high-throughput DNA FISH protocol to visualize genome regions in human cells
title_full_unstemmed A high-throughput DNA FISH protocol to visualize genome regions in human cells
title_short A high-throughput DNA FISH protocol to visualize genome regions in human cells
title_sort high-throughput dna fish protocol to visualize genome regions in human cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377592/
https://www.ncbi.nlm.nih.gov/pubmed/34458868
http://dx.doi.org/10.1016/j.xpro.2021.100741
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