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An open access, machine learning pipeline for high-throughput quantification of cell morphology

Cell morphology is influenced by many factors and can be used as a phenotypic marker. Here we describe a machine-learning-based protocol for high-throughput morphological measurement of human fibroblasts using a standard fluorescence microscope and the pre-existing, open access software ilastik for...

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Autores principales: Welter, Emma M., Kosyk, Oksana, Zannas, Anthony S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792532/
https://www.ncbi.nlm.nih.gov/pubmed/36527712
http://dx.doi.org/10.1016/j.xpro.2022.101947
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author Welter, Emma M.
Kosyk, Oksana
Zannas, Anthony S.
author_facet Welter, Emma M.
Kosyk, Oksana
Zannas, Anthony S.
author_sort Welter, Emma M.
collection PubMed
description Cell morphology is influenced by many factors and can be used as a phenotypic marker. Here we describe a machine-learning-based protocol for high-throughput morphological measurement of human fibroblasts using a standard fluorescence microscope and the pre-existing, open access software ilastik for cell body identification, ImageJ/Fiji for image overlay, and CellProfiler for morphological quantification. Because this protocol overlays nuclei with their cell bodies and relies on coloration differences, it can be broadly applied to other cell types beyond fibroblasts. For details on the use and execution of this protocol, please also refer to Leung et al. (2022).(1)
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spelling pubmed-97925322022-12-28 An open access, machine learning pipeline for high-throughput quantification of cell morphology Welter, Emma M. Kosyk, Oksana Zannas, Anthony S. STAR Protoc Protocol Cell morphology is influenced by many factors and can be used as a phenotypic marker. Here we describe a machine-learning-based protocol for high-throughput morphological measurement of human fibroblasts using a standard fluorescence microscope and the pre-existing, open access software ilastik for cell body identification, ImageJ/Fiji for image overlay, and CellProfiler for morphological quantification. Because this protocol overlays nuclei with their cell bodies and relies on coloration differences, it can be broadly applied to other cell types beyond fibroblasts. For details on the use and execution of this protocol, please also refer to Leung et al. (2022).(1) Elsevier 2022-12-15 /pmc/articles/PMC9792532/ /pubmed/36527712 http://dx.doi.org/10.1016/j.xpro.2022.101947 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Welter, Emma M.
Kosyk, Oksana
Zannas, Anthony S.
An open access, machine learning pipeline for high-throughput quantification of cell morphology
title An open access, machine learning pipeline for high-throughput quantification of cell morphology
title_full An open access, machine learning pipeline for high-throughput quantification of cell morphology
title_fullStr An open access, machine learning pipeline for high-throughput quantification of cell morphology
title_full_unstemmed An open access, machine learning pipeline for high-throughput quantification of cell morphology
title_short An open access, machine learning pipeline for high-throughput quantification of cell morphology
title_sort open access, machine learning pipeline for high-throughput quantification of cell morphology
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792532/
https://www.ncbi.nlm.nih.gov/pubmed/36527712
http://dx.doi.org/10.1016/j.xpro.2022.101947
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