Spatiotemporal-Aware Self-Supervised Fluorescence Microscopy Image Denoising

Fluorescence microscopy has been an indispensable tool in many scientific disciplines. However, the expensive imaging cost and the photo-toxicity problem make it difficult to obtain high-quality images. The independent shot noise in fluorescence microscopy images always overwhelms signals and limits the imaging resolution, hindering progress in related research. Recently, self-supervised image denoising has received wide attention for its ability to train a denoiser without paired low Signal-to-Noise Ratio (SNR) and high SNR images. Existing self-supervised fluorescence microscopy image denoising works either suffer from high imaging/computational cost or large training difficulty. Here, we propose a Single-image based Self-Supervised Denoising approach (TriS-D) by utilizing the spatiotemporal redundancy of the fluorescence microscopy imaging data, which facilitates the low-cost and convenient training. The TriS-D can generate the training data from a raw image, not only releasing the demand for multiple low SNR time-lapse imaging data but also enabling the building of a 2D convolution-based model. Comprehensive experiments across different imaging modalities and biological samples verify the effectiveness of the TriS-D.

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Publication Details

Journal
IEEE Signal Processing Letters
Published
2025-01-01
DOI
https://doi.org/10.1109/lsp.2025.3580043
Primary Topic
Cell Image Analysis Techniques
Type
article
Field-Weighted Citation Impact
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article

Spatiotemporal-Aware Self-Supervised Fluorescence Microscopy Image Denoising

Weimin Tan, Bo Yan, Zhaohui Zhou, Chenxi Ma
IEEE Signal Processing Letters
Cell Image Analysis Techniques
article

Spatiotemporal-Aware Self-Supervised Fluorescence Microscopy Image Denoising

Weimin Tan, Bo Yan, Zhaohui Zhou, Chenxi Ma
article en

Abstract

Fluorescence microscopy has been an indispensable tool in many scientific disciplines. However, the expensive imaging cost and the photo-toxicity problem make it difficult to obtain high-quality images. The independent shot noise in fluorescence microscopy images always overwhelms signals and limits the imaging resolution, hindering progress in related research. Recently, self-supervised image denoising has received wide attention for its ability to train a denoiser without paired low Signal-to-Noise Ratio (SNR) and high SNR images. Existing self-supervised fluorescence microscopy image denoising works either suffer from high imaging/computational cost or large training difficulty. Here, we propose a Single-image based Self-Supervised Denoising approach (TriS-D) by utilizing the spatiotemporal redundancy of the fluorescence microscopy imaging data, which facilitates the low-cost and convenient training. The TriS-D can generate the training data from a raw image, not only releasing the demand for multiple low SNR time-lapse imaging data but also enabling the building of a 2D convolution-based model. Comprehensive experiments across different imaging modalities and biological samples verify the effectiveness of the TriS-D.

IEEE Signal Processing LettersVol. 32
Waseda University (JP), Fudan University (CN)
Openalex Percentile: Top 90%
Cell Image Analysis Techniques
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