| Literature DB >> 31052759 |
Andres Flores Valle, Johannes D Seelig.
Abstract
Light microscopy on dynamic samples, for example neural activity in the brain, often requires imaging volumes that extend over several 100 µm in axial direction at a rate of at least several tens of Hertz. Here, we develop a tomography approach for scanning fluorescence microscopy which allows recording a volume image in a single frame scan. Volumes are imaged by simultaneously recording four independent projections at different angles using temporally multiplexed, tilted Bessel beams. From the resulting projections, three-dimensional images are reconstructed using inverse Radon transforms combined with convolutional neural networks (U-net).Year: 2019 PMID: 31052759 DOI: 10.1364/OE.27.012147
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894