| Literature DB >> 36163547 |
Xinyang Li1,2,3,4, Yixin Li3,5, Yiliang Zhou1,3, Jiamin Wu1,3,6,7, Zhifeng Zhao1,3, Jiaqi Fan2,3,8, Fei Deng9,10, Zhaofa Wu9,10, Guihua Xiao1,3, Jing He1,3, Yuanlong Zhang1,3, Guoxun Zhang1,3, Xiaowan Hu2, Xingye Chen1,3, Yi Zhang1,3, Hui Qiao1,3,6, Hao Xie1,3, Yulong Li9,10, Haoqian Wang11,12, Lu Fang13,14, Qionghai Dai15,16,17,18.
Abstract
A fundamental challenge in fluorescence microscopy is the photon shot noise arising from the inevitable stochasticity of photon detection. Noise increases measurement uncertainty and limits imaging resolution, speed and sensitivity. To achieve high-sensitivity fluorescence imaging beyond the shot-noise limit, we present DeepCAD-RT, a self-supervised deep learning method for real-time noise suppression. Based on our previous framework DeepCAD, we reduced the number of network parameters by 94%, memory consumption by 27-fold and processing time by a factor of 20, allowing real-time processing on a two-photon microscope. A high imaging signal-to-noise ratio can be acquired with tenfold fewer photons than in standard imaging approaches. We demonstrate the utility of DeepCAD-RT in a series of photon-limited experiments, including in vivo calcium imaging of mice, zebrafish larva and fruit flies, recording of three-dimensional (3D) migration of neutrophils after acute brain injury and imaging of 3D dynamics of cortical ATP release. DeepCAD-RT will facilitate the morphological and functional interrogation of biological dynamics with a minimal photon budget.Entities:
Year: 2022 PMID: 36163547 DOI: 10.1038/s41587-022-01450-8
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 68.164