显微镜
扫描电镜
数值孔径
显微镜
光学
全内反射荧光显微镜
人工智能
分辨率(逻辑)
荧光显微镜
荧光寿命成像显微镜
计算机科学
超分辨显微术
共焦
荧光
计算机视觉
超分辨率
薄层荧光显微镜
材料科学
光激活定位显微镜
物理
扫描共焦电子显微镜
图像(数学)
波长
作者
Hongda Wang,Yair Rivenson,Yiyin Jin,Zhensong Wei,Ronald Gao,Harun Günaydın,Laurent A. Bentolila,Cömert Kural,Aydogan Ozcan
出处
期刊:Nature Methods
[Springer Nature]
日期:2018-12-17
卷期号:16 (1): 103-110
被引量:598
标识
DOI:10.1038/s41592-018-0239-0
摘要
We present deep-learning-enabled super-resolution across different fluorescence microscopy modalities. This data-driven approach does not require numerical modeling of the imaging process or the estimation of a point-spread-function, and is based on training a generative adversarial network (GAN) to transform diffraction-limited input images into super-resolved ones. Using this framework, we improve the resolution of wide-field images acquired with low-numerical-aperture objectives, matching the resolution that is acquired using high-numerical-aperture objectives. We also demonstrate cross-modality super-resolution, transforming confocal microscopy images to match the resolution acquired with a stimulated emission depletion (STED) microscope. We further demonstrate that total internal reflection fluorescence (TIRF) microscopy images of subcellular structures within cells and tissues can be transformed to match the results obtained with a TIRF-based structured illumination microscope. The deep network rapidly outputs these super-resolved images, without any iterations or parameter search, and could serve to democratize super-resolution imaging.
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