Summary of ssbd-repos-000244

SSBD:database
URL

Name
ssbd-repos-000244 (244-Tokuoka-Embryogenesis)
URL
DOI
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Title
Time-series 3D images and BDML file for quantiative information about early mouse embryos with labeled nuclei.
Description
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Submited Date
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Release Date
2023-02-02
Updated Date
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License
Funding information
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File formats
Data size
250.8 MB

Organism
Mus musculus
Strain
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Cell Line
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Genes
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Proteins
H2B

GO Molecular Function (MF)
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GO Biological Process (BP)
embryo development
GO Cellular Component (CC)
nucleus
Study Type
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Imaging Methods
fluorescence microscopy, CV1000 microscope equipped with a 20x oil lens, IX71 microscope equipped with a 20x oil lens

Method Summary
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Related paper(s)

Yuta Tokuoka, Takahiro G Yamada, Daisuke Mashiko, Zenki Ikeda, Noriko F Hiroi, Tetsuya J Kobayashi, Kazuo Yamagata, Akira Funahashi (2020) 3D convolutional neural networks-based segmentation to acquire quantitative criteria of the nucleus during mouse embryogenesis., NPJ systems biology and applications, Volume 6, Number 1, pp. 32

Published in 2020 Oct 20 (Electronic publication in Oct. 20, 2020, midnight )

(Abstract) During embryogenesis, cells repeatedly divide and dynamically change their positions in three-dimensional (3D) space. A robust and accurate algorithm to acquire the 3D positions of the cells would help to reveal the mechanisms of embryogenesis. To acquire quantitative criteria of embryogenesis from time-series 3D microscopic images, image processing algorithms such as segmentation have been applied. Because the cells in embryos are considerably crowded, an algorithm to segment individual cells in detail and accurately is needed. To quantify the nuclear region of every cell from a time-series 3D fluorescence microscopic image of living cells, we developed QCANet, a convolutional neural network-based segmentation algorithm for 3D fluorescence bioimages. We demonstrated that QCANet outperformed 3D Mask R-CNN, which is currently considered as the best algorithm of instance segmentation. We showed that QCANet can be applied not only to developing mouse embryos but also to developing embryos of two other model species. Using QCANet, we were able to extract several quantitative criteria of embryogenesis from 11 early mouse embryos. We showed that the extracted criteria could be used to evaluate the differences between individual embryos. This study contributes to the development of fundamental approaches for assessing embryogenesis on the basis of extracted quantitative criteria.
(MeSH Terms)

Contact(s)
Akira Funahashi
Organization(s)
Keio University , Department of Biosciencesand Informatics
Image Data Contributors
Quantitative Data Contributors

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