A machine learning approach for single cell interphase cell cycle staging

Abstract The cell nucleus is a tightly regulated organelle and its architectural structure is dynamically orchestrated to maintain normal cell function. Indeed, fluctuations in nuclear size and shape are known to occur during the cell cycle and alterations in nuclear morphology are also hallmarks of...

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Autores principales: Hemaxi Narotamo, Maria Sofia Fernandes, Ana Margarida Moreira, Soraia Melo, Raquel Seruca, Margarida Silveira, João Miguel Sanches
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/ad30e0a2942d469a9a290f003248ca72
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spelling oai:doaj.org-article:ad30e0a2942d469a9a290f003248ca722021-12-02T17:37:12ZA machine learning approach for single cell interphase cell cycle staging10.1038/s41598-021-98489-52045-2322https://doaj.org/article/ad30e0a2942d469a9a290f003248ca722021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-98489-5https://doaj.org/toc/2045-2322Abstract The cell nucleus is a tightly regulated organelle and its architectural structure is dynamically orchestrated to maintain normal cell function. Indeed, fluctuations in nuclear size and shape are known to occur during the cell cycle and alterations in nuclear morphology are also hallmarks of many diseases including cancer. Regrettably, automated reliable tools for cell cycle staging at single cell level using in situ images are still limited. It is therefore urgent to establish accurate strategies combining bioimaging with high-content image analysis for a bona fide classification. In this study we developed a supervised machine learning method for interphase cell cycle staging of individual adherent cells using in situ fluorescence images of nuclei stained with DAPI. A Support Vector Machine (SVM) classifier operated over normalized nuclear features using more than 3500 DAPI stained nuclei. Molecular ground truth labels were obtained by automatic image processing using fluorescent ubiquitination-based cell cycle indicator (Fucci) technology. An average F1-Score of 87.7% was achieved with this framework. Furthermore, the method was validated on distinct cell types reaching recall values higher than 89%. Our method is a robust approach to identify cells in G1 or S/G2 at the individual level, with implications in research and clinical applications.Hemaxi NarotamoMaria Sofia FernandesAna Margarida MoreiraSoraia MeloRaquel SerucaMargarida SilveiraJoão Miguel SanchesNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hemaxi Narotamo
Maria Sofia Fernandes
Ana Margarida Moreira
Soraia Melo
Raquel Seruca
Margarida Silveira
João Miguel Sanches
A machine learning approach for single cell interphase cell cycle staging
description Abstract The cell nucleus is a tightly regulated organelle and its architectural structure is dynamically orchestrated to maintain normal cell function. Indeed, fluctuations in nuclear size and shape are known to occur during the cell cycle and alterations in nuclear morphology are also hallmarks of many diseases including cancer. Regrettably, automated reliable tools for cell cycle staging at single cell level using in situ images are still limited. It is therefore urgent to establish accurate strategies combining bioimaging with high-content image analysis for a bona fide classification. In this study we developed a supervised machine learning method for interphase cell cycle staging of individual adherent cells using in situ fluorescence images of nuclei stained with DAPI. A Support Vector Machine (SVM) classifier operated over normalized nuclear features using more than 3500 DAPI stained nuclei. Molecular ground truth labels were obtained by automatic image processing using fluorescent ubiquitination-based cell cycle indicator (Fucci) technology. An average F1-Score of 87.7% was achieved with this framework. Furthermore, the method was validated on distinct cell types reaching recall values higher than 89%. Our method is a robust approach to identify cells in G1 or S/G2 at the individual level, with implications in research and clinical applications.
format article
author Hemaxi Narotamo
Maria Sofia Fernandes
Ana Margarida Moreira
Soraia Melo
Raquel Seruca
Margarida Silveira
João Miguel Sanches
author_facet Hemaxi Narotamo
Maria Sofia Fernandes
Ana Margarida Moreira
Soraia Melo
Raquel Seruca
Margarida Silveira
João Miguel Sanches
author_sort Hemaxi Narotamo
title A machine learning approach for single cell interphase cell cycle staging
title_short A machine learning approach for single cell interphase cell cycle staging
title_full A machine learning approach for single cell interphase cell cycle staging
title_fullStr A machine learning approach for single cell interphase cell cycle staging
title_full_unstemmed A machine learning approach for single cell interphase cell cycle staging
title_sort machine learning approach for single cell interphase cell cycle staging
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/ad30e0a2942d469a9a290f003248ca72
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