| Literature DB >> 30478326 |
Martin Weigert1,2, Uwe Schmidt3,4, Tobias Boothe3,4, Andreas Müller5,6,7, Alexandr Dibrov3,4, Akanksha Jain4, Benjamin Wilhelm3,8, Deborah Schmidt3, Coleman Broaddus3,4, Siân Culley9,10, Mauricio Rocha-Martins3,4, Fabián Segovia-Miranda4, Caren Norden4, Ricardo Henriques9,10, Marino Zerial4, Michele Solimena4,5,6,7, Jochen Rink4, Pavel Tomancak4, Loic Royer11,12,13, Florian Jug14,15, Eugene W Myers3,4,16.
Abstract
Fluorescence microscopy is a key driver of discoveries in the life sciences, with observable phenomena being limited by the optics of the microscope, the chemistry of the fluorophores, and the maximum photon exposure tolerated by the sample. These limits necessitate trade-offs between imaging speed, spatial resolution, light exposure, and imaging depth. In this work we show how content-aware image restoration based on deep learning extends the range of biological phenomena observable by microscopy. We demonstrate on eight concrete examples how microscopy images can be restored even if 60-fold fewer photons are used during acquisition, how near isotropic resolution can be achieved with up to tenfold under-sampling along the axial direction, and how tubular and granular structures smaller than the diffraction limit can be resolved at 20-times-higher frame rates compared to state-of-the-art methods. All developed image restoration methods are freely available as open source software in Python, FIJI, and KNIME.Mesh:
Substances:
Year: 2018 PMID: 30478326 DOI: 10.1038/s41592-018-0216-7
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547