
1.Department of Automation, Tsinghua University, Beijing, 100084, China
2.Institute for Brain and Cognitive Sciences, Tsinghua University, Beijing, 100084, China
3.Beijing National Research Center for Information Science and Technology, Tsinghua University, Beijing, 100084, China
Jiamin Wu (wujiamin@tsinghua.edu.cn)
Qionghai Dai (qhdai@mail.tsinghua.edu.cn)
Published:31 August 2021,
Published Online:27 July 2021,
Received:05 December 2020,
Revised:04 June 2021,
Accepted:02 July 2021
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Zhang, Y. L. et al. DiLFM: an artifact-suppressed and noise-robust light-field microscopy through dictionary learning. Light: Science & Applications, 10, 1546-1557 (2021).
Zhang, Y. L. et al. DiLFM: an artifact-suppressed and noise-robust light-field microscopy through dictionary learning. Light: Science & Applications, 10, 1546-1557 (2021). DOI: 10.1038/s41377-021-00587-6.
Light field microscopy (LFM) has been widely used for recording 3D biological dynamics at camera frame rate. However
LFM suffers from artifact contaminations due to t
he illness of the reconstruction problem via naïve Richardson–Lucy (RL) deconvolution. Moreover
the performance of LFM significantly dropped in low-light conditions due to the absence of sample priors. In this paper
we thoroughly analyze different kinds of artifacts and present a new LFM technique termed dictionary LFM (DiLFM) that substantially suppresses various kinds of reconstruction artifacts and improves the noise robustness with an over-complete dictionary. We demonstrate artifact-suppressed reconstructions in scattering samples such as
Drosophila
embryos and brains. Furthermore
we show our DiLFM can achieve robust blood cell counting in noisy conditions by imaging blood cell dynamic at 100 Hz and unveil more neurons in whole-brain calcium recording of zebrafish with low illumination power in vivo.
Villette, V. et al. Ultrafast two-photon imaging of a high-gain voltage indicator in awake behaving mice.Cell179, 1590–1608 (2019). e23..
Dana, H. et al. High-performance calcium sensors for imaging activity in neuronal populations and microcompartments.Nat. Methods16, 649–657 (2019)..
Voleti, V. et al. Real-time volumetric microscopy of in vivo dynamics and large-scale samples with SCAPE 2.0.Nat. Methods16, 1054–1062 (2019)..
McDole, K. et al.In totoimaging and reconstruction of post-implantation mouse development at the single-cell level.Cell175, 859–876 (2018). e33..
Dey, N. et al. Richardson-Lucy algorithm with total variation regularization for 3D confocal microscope deconvolution.Microsc. Res. Tech.69, 260–266 (2006)..
McNally, J. G. et al. Three-dimensional imaging by deconvolution microscopy.Methods19, 373–385 (1999)..
Xu, C. et al. Multiphoton fluorescence excitation: new spectral windows for biological nonlinear microscopy.Proc. Natl Acad. Sci. USA93, 10763–10768 (1996)..
Keller, P. J. et al. Fast, high-contrast imaging of animal development with scanned light sheet-based structured-illumination microscopy.Nat. Methods7, 637–642 (2010)..
Gustafsson, M. G. L. Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution.Proc. Natl Acad. Sci. USA102, 13081–13086 (2005)..
Bewersdorf, J., Pick, R.&Hell, S. W. Multifocal multiphoton microscopy.Opt. Lett.23, 655–657 (1998)..
Prevedel, R. et al. Fast volumetric calcium imaging across multiple cortical layers using sculpted light.Nat. Methods13, 1021–1028 (2016)..
Salomé, R. et al. Ultrafast random-access scanning in two-photon microscopy using acousto-optic deflectors.J. Neurosci. Methods154, 161–174 (2006)..
Broxton, M. et al. Wave optics theory and 3-D deconvolution for the light field microscope.Opt. Express21, 25418–25439 (2013)..
Prevedel, R. et al. Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy.Nat. Methods11, 727–730 (2014)..
Levoy, M. et al. Light field microscopy.ACM Trans. Graph.25, 924–934 (2006)..
Lin, X. et al. Camera array based light field microscopy.Biomed. Opt. Express6, 3179–3189 (2015)..
Cong, L. et al. Rapid whole brain imaging of neural activity in freely behaving larval zebrafish (Danio rerio).eLife6, e28158 (2017)..
Li, H. Y. et al. Fast, volumetric live-cell imaging using high-resolution light-field microscopy.Biomed. Opt. Express10, 29–49 (2019)..
Guo, C. L. et al. Fourier light-field microscopy.Opt. Express27, 25573–25594 (2019)..
Richardson, W. H. Bayesian-based iterative method of image restoration.J. Opt. Soc. Am.62, 55–59 (1972)..
Lucy, L. B. An iterative technique for the rectification of observed distributions.Astron. J.79, 745 (1974)..
Wagner, N. et al. Instantaneous isotropic volumetric imaging of fast biological processes.Nat. Methods16, 497–500 (2019)..
Nöbauer, T. et al. Video rate volumetric Ca2+imaging across cortex using seeded iterative demixing (SID) microscopy.Nat. Methods14, 811–818 (2017)..
Pégard, N. C. et al. Compressive light-field microscopy for 3D neural activity recording.Optica3, 517–524 (2016)..
Cohen, N. et al. Enhancing the performance of the light field microscope using wavefront coding.Opt. Express22, 24817–24839 (2014)..
Wu, J. M. et al. Iterative tomography with digital adaptive optics permits hour-long intravital observation of 3D subcellular dynamics at millisecond scale.Cell(2021).
Skocek, O. et al. High-speed volumetric imaging of neuronal activity in freely moving rodents.Nat. Methods15, 429–432 (2018)..
Stefanoiu, A. et al. Artifact-free deconvolution in light field microscopy.Opt. Express27, 31644–31666 (2019)..
Lu, Z. et al. Phase-space deconvolution for light field microscopy.Opt. Express27, 18131–18145 (2019)..
Zeyde, R., Elad, M.&Protter, M. On single image scale-up using sparse-representations. inProc. 7th International Conference on Curves and Surfaces. (Springer, Avignon, 2012).
Wang, Z. et al. Image quality assessment: from error visibility to structural similarity.IEEE Trans. Image Process.13, 600–612 (2004)..
Zhou, P. C. et al. Efficient and accurate extraction of in vivo calcium signals from microendoscopic video data.eLife7, e28728 (2018)..
Zhang, Z. K. et al. Imaging volumetric dynamics at high speed in mouse and zebrafish brain with confocal light field microscopy.Nat. Biotechnol.39, 74–83 (2021)..
Liu, H. Y. et al. 3D imaging in volumetric scattering media using phase-space measurements.Opt. Express23, 14461–14471 (2015)..
Guo, C. L., Liu, W. H.&Jia, S. Fourier-domain light-field microscopy.Biophotonics Congress: Optics in the Life Sciences Congress2019. (OSA, Tucson, 2019)..
Gu, M.Advanced Optical Imaging Theory. (Springer, Berlin, 2000).
Zheng, W. et al. Adaptive optics improves multiphoton super-resolution imaging.Nat. Methods14, 869–872 (2017)..
Yang, J. C. et al. Image super-resolution via sparse representation.IEEE Trans. Image Process.19, 2861–2873 (2010)..
Aharon, M., Elad, M.&Bruckstein, A. K-SVD: an algorithm for designing overcomplete dictionaries for sparse representation.IEEE Trans. Signal Process.54, 4311–4322 (2006)..
Ljosa, V., Sokolnicki, K. L.&Carpenter, A. E. Annotated high-throughput microscopy image sets for validation.Nat. Methods9, 637 (2012)..
Kalinin, A. A. et al. 3D cell nuclear morphology: microscopy imaging dataset and voxel-based morphometry classification results. inProc. 2018 IEEE/CVF Conference on Computer Vision and Pattern Recognition Workshops. (IEEE, Salt Lake City, 2018).
Pati, Y. C., Rezaiifar, R.&Krishnaprasad, P. S. Orthogonal matching pursuit: recursive function approximation with applications to wavelet decomposition. inProc. 27th Asilomar Conference on Signals, Systems and Computers. (IEEE, Pacific Grove, 1993).
Rasal, T. et al. Mixed poisson gaussian noise reduction in fluorescence microscopy images using modified structure of wavelet transform.IET Image Process.15, 1383–1398 (2021)..
Pnevmatikakis, E. A. et al. Simultaneous denoising, deconvolution, and demixing of calcium imaging data.Neuron89, 285–299 (2016)..
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