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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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). |
format | Online Article Text |
id | pubmed-8377592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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