Abstract
Fluorescence microscopy enables the direct observation of previously hidden dynamic processes of life, allowing profound insights into mechanisms of health and disease. However, imaging of live samples is fundamentally limited by the toxicity of the illuminating light and images are often acquired using low light conditions. As a consequence, images can become very noisy which severely complicates their interpretation. In recent years, deep learning (DL) has emerged as a very successful approach to remove this noise while retaining the useful signal. Unlike classical algorithms which use well-defined mathematical functions to remove noise, DL methods learn to denoise from example data, providing a powerful content-aware approach. In this review, we first describe the different types of noise that typically corrupt fluorescence microscopy images and introduce the denoising task. We then present the main DL-based denoising methods and their relative advantages and disadvantages. We aim to provide insights into how DL-based denoising methods operate and help users choose the most appropriate tools for their applications.
Original language | English |
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Article number | 106077 |
Number of pages | 9 |
Journal | The International Journal of Biochemistry & Cell Biology |
Volume | 140 |
Early online date | 20 Sept 2021 |
DOIs | |
Publication status | Published - Nov 2021 |
Bibliographical note
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.Keywords
- Deep Learning
- Denoising
- Live-cell imaging
- Noise
- Microscopy