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Enhanced cell segmentation with limited annotated data using generative adversarial networks
The application of deep learning is rapidly transforming the field of bioimage analysis. While deep learning has shown great promise in complex microscopy tasks such as single-cell segmentation, the development of generalizable foundation deep learning segmentation models is hampered by the scarcity...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402092/ https://www.ncbi.nlm.nih.gov/pubmed/37546774 http://dx.doi.org/10.1101/2023.07.26.550715 |
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author | Zargari, Abolfazl Mashhadi, Najmeh Shariati, S. Ali |
author_facet | Zargari, Abolfazl Mashhadi, Najmeh Shariati, S. Ali |
author_sort | Zargari, Abolfazl |
collection | PubMed |
description | The application of deep learning is rapidly transforming the field of bioimage analysis. While deep learning has shown great promise in complex microscopy tasks such as single-cell segmentation, the development of generalizable foundation deep learning segmentation models is hampered by the scarcity of large and diverse annotated datasets of cell images for training purposes. Generative Adversarial Networks (GANs) can generate realistic images that can potentially be easily used to train deep learning models without the generation of large manually annotated microscopy images. Here, we propose a customized CycleGAN architecture to train an enhanced cell segmentation model with limited annotated cell images, effectively addressing the challenge of paucity of annotated data in microscopy imaging. Our customized CycleGAN model can generate realistic synthetic images of cells with morphological details and nuances very similar to that of real images. This method not only increases the variability seen during training but also enhances the authenticity of synthetic samples, thereby enhancing the overall predictive accuracy and robustness of the cell segmentation model. Our experimental results show that our CycleGAN-based method significantly improves the performance of the segmentation model compared to conventional training techniques. Interestingly, we demonstrate that our model can extrapolate its knowledge by synthesizing imaging scenarios that were not seen during the training process. Our proposed customized CycleGAN method will accelerate the development of foundation models for cell segmentation in microscopy images. |
format | Online Article Text |
id | pubmed-10402092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104020922023-08-05 Enhanced cell segmentation with limited annotated data using generative adversarial networks Zargari, Abolfazl Mashhadi, Najmeh Shariati, S. Ali bioRxiv Article The application of deep learning is rapidly transforming the field of bioimage analysis. While deep learning has shown great promise in complex microscopy tasks such as single-cell segmentation, the development of generalizable foundation deep learning segmentation models is hampered by the scarcity of large and diverse annotated datasets of cell images for training purposes. Generative Adversarial Networks (GANs) can generate realistic images that can potentially be easily used to train deep learning models without the generation of large manually annotated microscopy images. Here, we propose a customized CycleGAN architecture to train an enhanced cell segmentation model with limited annotated cell images, effectively addressing the challenge of paucity of annotated data in microscopy imaging. Our customized CycleGAN model can generate realistic synthetic images of cells with morphological details and nuances very similar to that of real images. This method not only increases the variability seen during training but also enhances the authenticity of synthetic samples, thereby enhancing the overall predictive accuracy and robustness of the cell segmentation model. Our experimental results show that our CycleGAN-based method significantly improves the performance of the segmentation model compared to conventional training techniques. Interestingly, we demonstrate that our model can extrapolate its knowledge by synthesizing imaging scenarios that were not seen during the training process. Our proposed customized CycleGAN method will accelerate the development of foundation models for cell segmentation in microscopy images. Cold Spring Harbor Laboratory 2023-07-28 /pmc/articles/PMC10402092/ /pubmed/37546774 http://dx.doi.org/10.1101/2023.07.26.550715 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Zargari, Abolfazl Mashhadi, Najmeh Shariati, S. Ali Enhanced cell segmentation with limited annotated data using generative adversarial networks |
title | Enhanced cell segmentation with limited annotated data using generative adversarial networks |
title_full | Enhanced cell segmentation with limited annotated data using generative adversarial networks |
title_fullStr | Enhanced cell segmentation with limited annotated data using generative adversarial networks |
title_full_unstemmed | Enhanced cell segmentation with limited annotated data using generative adversarial networks |
title_short | Enhanced cell segmentation with limited annotated data using generative adversarial networks |
title_sort | enhanced cell segmentation with limited annotated data using generative adversarial networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402092/ https://www.ncbi.nlm.nih.gov/pubmed/37546774 http://dx.doi.org/10.1101/2023.07.26.550715 |
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