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Main Authors: Wang, Mengrui, Shu, Manming, Yan, Jiajing, Liu, Chang, Fu, Xiangda, Zhang, Jingxiang, Lin, Yuchen, Zhao, Hu, Huang, Yuwei, Ma, Dingbang, Ge, Yifan, Hao, Huiwen, Zhao, Tianyu, Liang, Yansheng, Wang, Shaowei, Lei, Ming
Format: Preprint
Published: 2024
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Online Access:https://arxiv.org/abs/2412.05677
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author Wang, Mengrui
Shu, Manming
Yan, Jiajing
Liu, Chang
Fu, Xiangda
Zhang, Jingxiang
Lin, Yuchen
Zhao, Hu
Huang, Yuwei
Ma, Dingbang
Ge, Yifan
Hao, Huiwen
Zhao, Tianyu
Liang, Yansheng
Wang, Shaowei
Lei, Ming
author_facet Wang, Mengrui
Shu, Manming
Yan, Jiajing
Liu, Chang
Fu, Xiangda
Zhang, Jingxiang
Lin, Yuchen
Zhao, Hu
Huang, Yuwei
Ma, Dingbang
Ge, Yifan
Hao, Huiwen
Zhao, Tianyu
Liang, Yansheng
Wang, Shaowei
Lei, Ming
contents Three-dimensional (3D) fluorescence imaging provides a vital approach for study of biological tissues with intricate structures, and optical sectioning structured illumination microscopy (OS-SIM) stands out for its high imaging speed, low phototoxicity and high spatial resolution. However, OS-SIM faces the problem of low signal-to-noise ratio (SNR) when using traditional decoding algorithms, especially in thick tissues. Here we propose a Hilbert-transform decoding and space domain based high-low (HT-SHiLo) algorithm for noise suppression in OS-SIM. We demonstrate HT-SHiLo algorithm can significantly improve the SNR of optical sectioning images at rapid processing speed, and double the imaging depth in thick tissues. With our OS-SIM system, we achieve high quality 3D images of various biological samples including mouse brains, Drosophila clock neurons, organoids, and live cells. We anticipate that this approach will render OS-SIM a powerful technique for research of cellular organelles or thick tissues in 3D morphology.
format Preprint
id arxiv_https___arxiv_org_abs_2412_05677
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle High SNR 3D Imaging from Millimeter-scale Thick Tissues to Cellular Dynamics via Structured Illumination Microscopy
Wang, Mengrui
Shu, Manming
Yan, Jiajing
Liu, Chang
Fu, Xiangda
Zhang, Jingxiang
Lin, Yuchen
Zhao, Hu
Huang, Yuwei
Ma, Dingbang
Ge, Yifan
Hao, Huiwen
Zhao, Tianyu
Liang, Yansheng
Wang, Shaowei
Lei, Ming
Optics
Three-dimensional (3D) fluorescence imaging provides a vital approach for study of biological tissues with intricate structures, and optical sectioning structured illumination microscopy (OS-SIM) stands out for its high imaging speed, low phototoxicity and high spatial resolution. However, OS-SIM faces the problem of low signal-to-noise ratio (SNR) when using traditional decoding algorithms, especially in thick tissues. Here we propose a Hilbert-transform decoding and space domain based high-low (HT-SHiLo) algorithm for noise suppression in OS-SIM. We demonstrate HT-SHiLo algorithm can significantly improve the SNR of optical sectioning images at rapid processing speed, and double the imaging depth in thick tissues. With our OS-SIM system, we achieve high quality 3D images of various biological samples including mouse brains, Drosophila clock neurons, organoids, and live cells. We anticipate that this approach will render OS-SIM a powerful technique for research of cellular organelles or thick tissues in 3D morphology.
title High SNR 3D Imaging from Millimeter-scale Thick Tissues to Cellular Dynamics via Structured Illumination Microscopy
topic Optics
url https://arxiv.org/abs/2412.05677