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High-throughput, image-based screening of pooled genetic variant libraries
Image-based, high-throughput screening of genetic perturbations will advance both biology and biotechnology. We report a high-throughput screening method that allows diverse genotypes and corresponding phenotypes to be imaged in numerous individual cells. We achieve genotyping by introducing barcode...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958624/ https://www.ncbi.nlm.nih.gov/pubmed/29083401 http://dx.doi.org/10.1038/nmeth.4495 |
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author | Emanuel, George Moffitt, Jeffrey R. Zhuang, Xiaowei |
author_facet | Emanuel, George Moffitt, Jeffrey R. Zhuang, Xiaowei |
author_sort | Emanuel, George |
collection | PubMed |
description | Image-based, high-throughput screening of genetic perturbations will advance both biology and biotechnology. We report a high-throughput screening method that allows diverse genotypes and corresponding phenotypes to be imaged in numerous individual cells. We achieve genotyping by introducing barcoded genetic variants into cells and using massively multiplexed FISH to measure the barcodes. We demonstrated this method by screening mutants of the fluorescent protein YFAST, yielding brighter and more photostable YFAST variants. |
format | Online Article Text |
id | pubmed-5958624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59586242018-05-18 High-throughput, image-based screening of pooled genetic variant libraries Emanuel, George Moffitt, Jeffrey R. Zhuang, Xiaowei Nat Methods Article Image-based, high-throughput screening of genetic perturbations will advance both biology and biotechnology. We report a high-throughput screening method that allows diverse genotypes and corresponding phenotypes to be imaged in numerous individual cells. We achieve genotyping by introducing barcoded genetic variants into cells and using massively multiplexed FISH to measure the barcodes. We demonstrated this method by screening mutants of the fluorescent protein YFAST, yielding brighter and more photostable YFAST variants. 2017-10-30 2017-12 /pmc/articles/PMC5958624/ /pubmed/29083401 http://dx.doi.org/10.1038/nmeth.4495 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Emanuel, George Moffitt, Jeffrey R. Zhuang, Xiaowei High-throughput, image-based screening of pooled genetic variant libraries |
title | High-throughput, image-based screening of pooled genetic variant libraries |
title_full | High-throughput, image-based screening of pooled genetic variant libraries |
title_fullStr | High-throughput, image-based screening of pooled genetic variant libraries |
title_full_unstemmed | High-throughput, image-based screening of pooled genetic variant libraries |
title_short | High-throughput, image-based screening of pooled genetic variant libraries |
title_sort | high-throughput, image-based screening of pooled genetic variant libraries |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958624/ https://www.ncbi.nlm.nih.gov/pubmed/29083401 http://dx.doi.org/10.1038/nmeth.4495 |
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