Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
Structured illumination microscopy (SIM) with axially optical sectioning capability has found widespread applications in three-dimensional live cell imaging in recent years, since it combines high sensitivity, short image acquisition time, and high spatial resolution. To obtain one sectioned slice,...
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doaj-9901ab8f8d4545a9a395e2dc569a199b2020-11-25T02:45:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012089210.1371/journal.pone.0120892Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.Xing ZhouMing LeiDan DanBaoli YaoJia QianShaohui YanYanlong YangJunwei MinTong PengTong YeGuangde ChenStructured illumination microscopy (SIM) with axially optical sectioning capability has found widespread applications in three-dimensional live cell imaging in recent years, since it combines high sensitivity, short image acquisition time, and high spatial resolution. To obtain one sectioned slice, three raw images with a fixed phase-shift, normally 2π/3, are generally required. In this paper, we report a data processing algorithm based on the one-dimensional Hilbert transform, which needs only two raw images with arbitrary phase-shift for each single slice. The proposed algorithm is different from the previous two-dimensional Hilbert spiral transform algorithm in theory. The presented algorithm has the advantages of simpler data processing procedure, faster computation speed and better reconstructed image quality. The validity of the scheme is verified by imaging biological samples in our developed DMD-based LED-illumination SIM system.http://europepmc.org/articles/PMC4370656?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xing Zhou Ming Lei Dan Dan Baoli Yao Jia Qian Shaohui Yan Yanlong Yang Junwei Min Tong Peng Tong Ye Guangde Chen |
spellingShingle |
Xing Zhou Ming Lei Dan Dan Baoli Yao Jia Qian Shaohui Yan Yanlong Yang Junwei Min Tong Peng Tong Ye Guangde Chen Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction. PLoS ONE |
author_facet |
Xing Zhou Ming Lei Dan Dan Baoli Yao Jia Qian Shaohui Yan Yanlong Yang Junwei Min Tong Peng Tong Ye Guangde Chen |
author_sort |
Xing Zhou |
title |
Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction. |
title_short |
Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction. |
title_full |
Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction. |
title_fullStr |
Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction. |
title_full_unstemmed |
Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction. |
title_sort |
double-exposure optical sectioning structured illumination microscopy based on hilbert transform reconstruction. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2015-01-01 |
description |
Structured illumination microscopy (SIM) with axially optical sectioning capability has found widespread applications in three-dimensional live cell imaging in recent years, since it combines high sensitivity, short image acquisition time, and high spatial resolution. To obtain one sectioned slice, three raw images with a fixed phase-shift, normally 2π/3, are generally required. In this paper, we report a data processing algorithm based on the one-dimensional Hilbert transform, which needs only two raw images with arbitrary phase-shift for each single slice. The proposed algorithm is different from the previous two-dimensional Hilbert spiral transform algorithm in theory. The presented algorithm has the advantages of simpler data processing procedure, faster computation speed and better reconstructed image quality. The validity of the scheme is verified by imaging biological samples in our developed DMD-based LED-illumination SIM system. |
url |
http://europepmc.org/articles/PMC4370656?pdf=render |
work_keys_str_mv |
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