Abstract
Image noise is a fundamental problem in fluorescence microscopy analysis, especially in live cell imaging applications where the number of detected photons is limited due to low power of excitation lasers to prevent phototoxicity during extended imaging experiments. The noise increases measurement uncertainty and complicates further image processing routines such as deconvolution, object detection and segmentation. State-of-the-art denoisers are computationally expensive and require training using large datasets, which are not available in cases of typical biological imaging experiments with rather scarce and unlabelled data. Here, we show that a denoiser can be trained using a single image containing a cropped out object of interest, where we exploit the symmetry often present in biological structures at molecular scales. As only a single example is used during training, our method can be trained even with limited computational resources, obtaining competitive denoising performance compared to the state-of-the-art methods.
| Original language | English |
|---|---|
| Journal | Journal of Microscopy |
| DOIs | |
| Publication status | E-pub ahead of print - 23 Jan 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Author(s). Journal of Microscopy published by John Wiley & Sons Ltd on behalf of Royal Microscopical Society.
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