4.8 Article

Evaluation and development of deep neural networks for image super-resolution in optical microscopy

期刊

NATURE METHODS
卷 18, 期 2, 页码 194-+

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41592-020-01048-5

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资金

  1. National Natural Science Foundation of China (NSFC) [91754202, 31827802, 31800717, 62088102]
  2. Ministry of Science and Technology (MOST) [2017YFA0505301, 2016YFA0500203]
  3. Chinese Academy of Sciences (CAS) [XDB19040101, ZDBS-LY-SM004]
  4. Youth Innovation Promotion Association of Chinese Academy of Sciences [2020094]
  5. China Postdoctoral Science Foundation [BX20190355]
  6. Tencent Foundation through the XPLORER PRIZE

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This study investigates the performance of deep-learning models for super-resolution imaging, introducing models that utilize frequency content information in the Fourier domain to improve imaging under low-SNR conditions. The research shows that deep-learning models can robustly reconstruct SIM images under low signal-to-noise ratio conditions, achieving comparable image quality to SIM in multicolor live-cell imaging experiments.
This study explores the performance of deep-learning models for super-resolution imaging and introduces models that utilize frequency content information in the Fourier domain to improve SIM reconstruction under low-SNR conditions. Deep neural networks have enabled astonishing transformations from low-resolution (LR) to super-resolved images. However, whether, and under what imaging conditions, such deep-learning models outperform super-resolution (SR) microscopy is poorly explored. Here, using multimodality structured illumination microscopy (SIM), we first provide an extensive dataset of LR-SR image pairs and evaluate the deep-learning SR models in terms of structural complexity, signal-to-noise ratio and upscaling factor. Second, we devise the deep Fourier channel attention network (DFCAN), which leverages the frequency content difference across distinct features to learn precise hierarchical representations of high-frequency information about diverse biological structures. Third, we show that DFCAN's Fourier domain focalization enables robust reconstruction of SIM images under low signal-to-noise ratio conditions. We demonstrate that DFCAN achieves comparable image quality to SIM over a tenfold longer duration in multicolor live-cell imaging experiments, which reveal the detailed structures of mitochondrial cristae and nucleoids and the interaction dynamics of organelles and cytoskeleton.

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