Calibration-free single-frame super-resolution fluorescence microscopy
Ane\v{z}ka Dost\'alov\'a, Dominik Va\v{s}inka, Robert St\'arek, Miroslav Je\v{z}ek

TL;DR
This paper introduces a deep learning method that reconstructs super-resolution fluorescence images from a single camera frame without calibration, enabling faster and more versatile nanoscale imaging.
Contribution
The authors develop a synthetic-data-trained deep learning model that generalizes across microscopes and conditions for single-frame super-resolution microscopy.
Findings
Achieves 7-fold resolution improvement beyond Rayleigh limit.
Reduces reconstruction error compared to traditional methods.
Demonstrates robustness across noise, aberrations, and optical parameters.
Abstract
Molecular fluorescence microscopy is a leading approach to super-resolution and nanoscale imaging in life and material sciences. However, super-resolution fluorescence microscopy is often bottlenecked by system-specific calibrations and long acquisitions of sparsely blinking molecules. We present a deep-learning approach that reconstructs super-resolved images directly from a single diffraction-limited camera frame. The model is trained exclusively on synthetic data encompassing a wide range of optical and sample parameters, enabling robust generalization across microscopes and experimental conditions. Applied to dense terrylene samples with 150 ms acquisition time, our method significantly reduces reconstruction error compared to Richardson-Lucy deconvolution and ThunderSTORM multi-emitter fitting. The results confirm the ability to resolve emitters separated by 35 nm at 580 nm…
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Taxonomy
TopicsAdvanced Fluorescence Microscopy Techniques · Digital Holography and Microscopy · Near-Field Optical Microscopy
