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Ultrasound Despeckling With GANs and Cross Modality Transfer Learning
- Source :
- IEEE Access, Vol 12, Pp 45811-45823 (2024)
- Publication Year :
- 2024
- Publisher :
- IEEE, 2024.
-
Abstract
- Ultrasound images are corrupted by a type of signal-dependent noise, called speckle, difficult to remove or attenuate with the classical denoising methods. On the contrary, structural Magnetic Resonance Imaging (MRI) is usually a high resolution low noise image modality that involves complex and expensive equipment and long acquisition times. Herein, a deep learning-based pipeline for speckle removal in B-mode ultrasound medical images, based on cross modality transfer learning, is proposed. The architecture of the system is based on a pix2pix Generative Adversarial Network (GAN), $D$ , able to denoise real B-mode ultrasound images by generating synthetic MRI-like versions by an image-to-image translation manner. The GAN $D$ was trained using two classes of image pairs: i) a set consisting of authentic MRI images paired with synthetic ultrasound images generated through a dedicated ultrasound simulator based on another GAN, $S$ , designed specifically for this purpose, and ii) a set comprising natural images paired with their corresponding noisy counterparts corrupted by Rayleigh noise. The denoising GAN proposed in this study demonstrates effective removal of speckle noise from B-mode ultrasound images. It successfully preserves the integrity of anatomical structures and avoids reconstruction artifacts, producing outputs that closely resemble typical MRI images. Comparative tests against other state-of-the-art methods reveal superior performance of the proposed denoising strategy across various reconstruction quality metrics.
Details
- Language :
- English
- ISSN :
- 21693536
- Volume :
- 12
- Database :
- Directory of Open Access Journals
- Journal :
- IEEE Access
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.5f6d338e0244afa1e7ff922c2323c3
- Document Type :
- article
- Full Text :
- https://doi.org/10.1109/ACCESS.2024.3381630