
1.SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St Andrews, Fife KY16 9SS, UK
2.Robinson Research Institute, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia
3.Australian Research Council Centre of Excellence for Nanoscale BioPhotonics, The University of Adelaide, Adelaide, SA, Australia
4.Institute for Photonics and Advanced Sensing, The University of Adelaide, Adelaide, SA, Australia
5.Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0RE, UK
6.School of Biological Sciences, The University of Adelaide, Adelaide, SA, Australia
7.Department of Physics, College of Science, Yonsei University, Seoul 03722, South Korea
Philip Wijesinghe (pw64@st-andrews.ac.uk)
Kishan Dholakia (kd1@st-andrews.ac.uk)
Published:30 November 2022,
Published Online:02 November 2022,
Received:09 August 2021,
Revised:26 August 2022,
Accepted:31 August 2022
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Wijesinghe, P. et al. Experimentally unsupervised deconvolution for light-sheet microscopy with propagation-invariant beams. Light: Science & Applications, 11, 2790-2804 (2022).
Wijesinghe, P. et al. Experimentally unsupervised deconvolution for light-sheet microscopy with propagation-invariant beams. Light: Science & Applications, 11, 2790-2804 (2022). DOI: 10.1038/s41377-022-00975-6.
Deconvolution is a challenging inverse problem
particularly in techniques that employ complex engineered point-spread functions
such as microscopy with propagation-invariant beams. Here
we present a deep-learning method for deconvolution that
in lieu of end-to-end training with ground truths
is trained using known physics of the imaging system. Specifically
we train a generative adversarial network with images generated with the known point-spread function of the system
and combine this with unpaired experimental data that preserve perceptual content. Our method rapidly and robustly deconvolves and super-resolves microscopy images
demonstrating a two-fold improvement in image contrast to conventional deconvolution methods. In contrast to common end-to-end networks that often require 1000–10
000s paired images
our method is experimentally unsupervised and can be trained solely on a few hundred regions of interest. We demonstrate its performance on light-sheet microscopy with propagation-invariant Airy beams in oocytes
preimplantation embryos and excised brain tissue
as well as illustrate its utility for Bessel-beam LSM. This method aims to democratise learned methods for deconvolution
as it does not require data acquisition outwith the conventional imaging protocol.
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