Deep Learning-Based Point-Scanning Super-Resolution Imaging

Linjing Fang(Salk Institute for Biological Studies), Fred Monroe, Sammy Weiser Novak(Salk Institute for Biological Studies), Lyndsey M. Kirk(The University of Texas at Austin), Cara R. Schiavon(Salk Institute for Biological Studies), Seungyoon B. Yu(University of California San Diego), Tong Zhang(Salk Institute for Biological Studies), Melissa Wu(Salk Institute for Biological Studies), Kyle Kastner(Concordia University), Yoshiyuki Kubota(National Institute for Physiological Sciences), Zhao Zhang, Gülçin Pekkurnaz(University of California San Diego), John M. Mendenhall(The University of Texas at Austin), Kristen M. Harris(The University of Texas at Austin), Jeremy Howard(University of San Francisco), Uri Manor(Salk Institute for Biological Studies)
bioRxiv (Cold Spring Harbor Laboratory)
August 21, 2019
Cited by 47Open Access
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Abstract

Point scanning imaging systems (e.g. scanning electron or laser scanning confocal microscopes) are perhaps the most widely used tools for high resolution cellular and tissue imaging. Like all other imaging modalities, the resolution, speed, sample preservation, and signal-to-noise ratio (SNR) of point scanning systems are difficult to optimize simultaneously. In particular, point scanning systems are uniquely constrained by an inverse relationship between imaging speed and pixel resolution. Here we show these limitations can be mitigated via the use of deep learning-based super-sampling of undersampled images acquired on a point-scanning system, which we termed point-scanning super-resolution (PSSR) imaging. Oversampled, high SNR ground truth images acquired on scanning electron or Airyscan laser scanning confocal microscopes were "crappified" to generate semi-synthetic training data for PSSR models that were then used to restore real-world undersampled images. Remarkably, our EM PSSR model could restore undersampled images acquired with different optics, detectors, samples, or sample preparation methods in other labs. PSSR enabled previously unattainable 2 nm resolution images with our serial block face scanning electron microscope system. For fluorescence, we show that undersampled confocal images combined with a multiframe PSSR model trained on Airyscan timelapses facilitates Airyscan-equivalent spatial resolution and SNR with ~100x lower laser dose and 16x higher frame rates than corresponding high-resolution acquisitions. In conclusion, PSSR facilitates point-scanning image acquisition with otherwise unattainable resolution, speed, and sensitivity.


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