Cell sorters see things more clearly now

Abstract Microscopy and fluorescence‐activated cell sorting (FACS) are two of the most important tools for single‐cell phenotyping in basic and biomedical research. Microscopy provides high‐resolution snapshots of cell morphology and the inner workings of cells, while FACS isolates thousands of cell...

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Main Authors: Daniel Schraivogel, Lars M Steinmetz
Format: Article
Language:English
Published: Springer Nature 2023-02-01
Series:Molecular Systems Biology
Online Access:https://doi.org/10.15252/msb.202211254
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author Daniel Schraivogel
Lars M Steinmetz
author_facet Daniel Schraivogel
Lars M Steinmetz
author_sort Daniel Schraivogel
collection DOAJ
description Abstract Microscopy and fluorescence‐activated cell sorting (FACS) are two of the most important tools for single‐cell phenotyping in basic and biomedical research. Microscopy provides high‐resolution snapshots of cell morphology and the inner workings of cells, while FACS isolates thousands of cells per second using simple parameters, such as the intensity of fluorescent protein labels. Recent technologies are now combining both methods to enable the fast isolation of cells with microscopic phenotypes of interest, thereby bridging a long‐standing gap in the life sciences. In this Commentary, we discuss the technical advancements made by image‐enabled cell sorting and highlight novel experimental strategies in functional genomics and single‐cell research.
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spelling doaj-art-ffbefa27a0b54fa8abae856bb7f513d32025-08-20T03:46:41ZengSpringer NatureMolecular Systems Biology1744-42922023-02-011931410.15252/msb.202211254Cell sorters see things more clearly nowDaniel Schraivogel0Lars M Steinmetz1Genome Biology Unit, European Molecular Biology Laboratory (EMBL)Genome Biology Unit, European Molecular Biology Laboratory (EMBL)Abstract Microscopy and fluorescence‐activated cell sorting (FACS) are two of the most important tools for single‐cell phenotyping in basic and biomedical research. Microscopy provides high‐resolution snapshots of cell morphology and the inner workings of cells, while FACS isolates thousands of cells per second using simple parameters, such as the intensity of fluorescent protein labels. Recent technologies are now combining both methods to enable the fast isolation of cells with microscopic phenotypes of interest, thereby bridging a long‐standing gap in the life sciences. In this Commentary, we discuss the technical advancements made by image‐enabled cell sorting and highlight novel experimental strategies in functional genomics and single‐cell research.https://doi.org/10.15252/msb.202211254
spellingShingle Daniel Schraivogel
Lars M Steinmetz
Cell sorters see things more clearly now
Molecular Systems Biology
title Cell sorters see things more clearly now
title_full Cell sorters see things more clearly now
title_fullStr Cell sorters see things more clearly now
title_full_unstemmed Cell sorters see things more clearly now
title_short Cell sorters see things more clearly now
title_sort cell sorters see things more clearly now
url https://doi.org/10.15252/msb.202211254
work_keys_str_mv AT danielschraivogel cellsortersseethingsmoreclearlynow
AT larsmsteinmetz cellsortersseethingsmoreclearlynow