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Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy
Volumetric imaging by fluorescence microscopy is often limited by anisotropic spatial resolution, in which the axial resolution is inferior to the lateral resolution. To address this problem, we present a deep-learning-enabled unsupervised super-resolution technique that enhances anisotropic images...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9178036/ https://www.ncbi.nlm.nih.gov/pubmed/35676288 http://dx.doi.org/10.1038/s41467-022-30949-6 |
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author | Park, Hyoungjun Na, Myeongsu Kim, Bumju Park, Soohyun Kim, Ki Hean Chang, Sunghoe Ye, Jong Chul |
author_facet | Park, Hyoungjun Na, Myeongsu Kim, Bumju Park, Soohyun Kim, Ki Hean Chang, Sunghoe Ye, Jong Chul |
author_sort | Park, Hyoungjun |
collection | PubMed |
description | Volumetric imaging by fluorescence microscopy is often limited by anisotropic spatial resolution, in which the axial resolution is inferior to the lateral resolution. To address this problem, we present a deep-learning-enabled unsupervised super-resolution technique that enhances anisotropic images in volumetric fluorescence microscopy. In contrast to the existing deep learning approaches that require matched high-resolution target images, our method greatly reduces the effort to be put into practice as the training of a network requires only a single 3D image stack, without a priori knowledge of the image formation process, registration of training data, or separate acquisition of target data. This is achieved based on the optimal transport-driven cycle-consistent generative adversarial network that learns from an unpaired matching between high-resolution 2D images in the lateral image plane and low-resolution 2D images in other planes. Using fluorescence confocal microscopy and light-sheet microscopy, we demonstrate that the trained network not only enhances axial resolution but also restores suppressed visual details between the imaging planes and removes imaging artifacts. |
format | Online Article Text |
id | pubmed-9178036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91780362022-06-10 Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy Park, Hyoungjun Na, Myeongsu Kim, Bumju Park, Soohyun Kim, Ki Hean Chang, Sunghoe Ye, Jong Chul Nat Commun Article Volumetric imaging by fluorescence microscopy is often limited by anisotropic spatial resolution, in which the axial resolution is inferior to the lateral resolution. To address this problem, we present a deep-learning-enabled unsupervised super-resolution technique that enhances anisotropic images in volumetric fluorescence microscopy. In contrast to the existing deep learning approaches that require matched high-resolution target images, our method greatly reduces the effort to be put into practice as the training of a network requires only a single 3D image stack, without a priori knowledge of the image formation process, registration of training data, or separate acquisition of target data. This is achieved based on the optimal transport-driven cycle-consistent generative adversarial network that learns from an unpaired matching between high-resolution 2D images in the lateral image plane and low-resolution 2D images in other planes. Using fluorescence confocal microscopy and light-sheet microscopy, we demonstrate that the trained network not only enhances axial resolution but also restores suppressed visual details between the imaging planes and removes imaging artifacts. Nature Publishing Group UK 2022-06-08 /pmc/articles/PMC9178036/ /pubmed/35676288 http://dx.doi.org/10.1038/s41467-022-30949-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Park, Hyoungjun Na, Myeongsu Kim, Bumju Park, Soohyun Kim, Ki Hean Chang, Sunghoe Ye, Jong Chul Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
title | Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
title_full | Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
title_fullStr | Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
title_full_unstemmed | Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
title_short | Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
title_sort | deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9178036/ https://www.ncbi.nlm.nih.gov/pubmed/35676288 http://dx.doi.org/10.1038/s41467-022-30949-6 |
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