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A deep learning-based algorithm for 2-D cell segmentation in microscopy images

BACKGROUND: Automatic and reliable characterization of cells in cell cultures is key to several applications such as cancer research and drug discovery. Given the recent advances in light microscopy and the need for accurate and high-throughput analysis of cells, automated algorithms have been devel...

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Autores principales: Al-Kofahi, Yousef, Zaltsman, Alla, Graves, Robert, Marshall, Will, Rusu, Mirabela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171227/
https://www.ncbi.nlm.nih.gov/pubmed/30285608
http://dx.doi.org/10.1186/s12859-018-2375-z
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author Al-Kofahi, Yousef
Zaltsman, Alla
Graves, Robert
Marshall, Will
Rusu, Mirabela
author_facet Al-Kofahi, Yousef
Zaltsman, Alla
Graves, Robert
Marshall, Will
Rusu, Mirabela
author_sort Al-Kofahi, Yousef
collection PubMed
description BACKGROUND: Automatic and reliable characterization of cells in cell cultures is key to several applications such as cancer research and drug discovery. Given the recent advances in light microscopy and the need for accurate and high-throughput analysis of cells, automated algorithms have been developed for segmenting and analyzing the cells in microscopy images. Nevertheless, accurate, generic and robust whole-cell segmentation is still a persisting need to precisely quantify its morphological properties, phenotypes and sub-cellular dynamics. RESULTS: We present a single-channel whole cell segmentation algorithm. We use markers that stain the whole cell, but with less staining in the nucleus, and without using a separate nuclear stain. We show the utility of our approach in microscopy images of cell cultures in a wide variety of conditions. Our algorithm uses a deep learning approach to learn and predict locations of the cells and their nuclei, and combines that with thresholding and watershed-based segmentation. We trained and validated our approach using different sets of images, containing cells stained with various markers and imaged at different magnifications. Our approach achieved a 86% similarity to ground truth segmentation when identifying and separating cells. CONCLUSIONS: The proposed algorithm is able to automatically segment cells from single channel images using a variety of markers and magnifications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2375-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-61712272018-10-10 A deep learning-based algorithm for 2-D cell segmentation in microscopy images Al-Kofahi, Yousef Zaltsman, Alla Graves, Robert Marshall, Will Rusu, Mirabela BMC Bioinformatics Methodology Article BACKGROUND: Automatic and reliable characterization of cells in cell cultures is key to several applications such as cancer research and drug discovery. Given the recent advances in light microscopy and the need for accurate and high-throughput analysis of cells, automated algorithms have been developed for segmenting and analyzing the cells in microscopy images. Nevertheless, accurate, generic and robust whole-cell segmentation is still a persisting need to precisely quantify its morphological properties, phenotypes and sub-cellular dynamics. RESULTS: We present a single-channel whole cell segmentation algorithm. We use markers that stain the whole cell, but with less staining in the nucleus, and without using a separate nuclear stain. We show the utility of our approach in microscopy images of cell cultures in a wide variety of conditions. Our algorithm uses a deep learning approach to learn and predict locations of the cells and their nuclei, and combines that with thresholding and watershed-based segmentation. We trained and validated our approach using different sets of images, containing cells stained with various markers and imaged at different magnifications. Our approach achieved a 86% similarity to ground truth segmentation when identifying and separating cells. CONCLUSIONS: The proposed algorithm is able to automatically segment cells from single channel images using a variety of markers and magnifications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2375-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-03 /pmc/articles/PMC6171227/ /pubmed/30285608 http://dx.doi.org/10.1186/s12859-018-2375-z Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Al-Kofahi, Yousef
Zaltsman, Alla
Graves, Robert
Marshall, Will
Rusu, Mirabela
A deep learning-based algorithm for 2-D cell segmentation in microscopy images
title A deep learning-based algorithm for 2-D cell segmentation in microscopy images
title_full A deep learning-based algorithm for 2-D cell segmentation in microscopy images
title_fullStr A deep learning-based algorithm for 2-D cell segmentation in microscopy images
title_full_unstemmed A deep learning-based algorithm for 2-D cell segmentation in microscopy images
title_short A deep learning-based algorithm for 2-D cell segmentation in microscopy images
title_sort deep learning-based algorithm for 2-d cell segmentation in microscopy images
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171227/
https://www.ncbi.nlm.nih.gov/pubmed/30285608
http://dx.doi.org/10.1186/s12859-018-2375-z
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