F3-Net combines multi-encoder nnU-Net with zero-filled missing modalities to segment glioma, metastasis, stroke, and white matter lesions, but the missing-modality claim is untested and comparisons are incomplete.
VIS-MAE: An Efficient Self-supervised Learning Approach on Medical Image Segmentation and Classification
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abstract
Artificial Intelligence (AI) has the potential to revolutionize diagnosis and segmentation in medical imaging. However, development and clinical implementation face multiple challenges including limited data availability, lack of generalizability, and the necessity to incorporate multi-modal data effectively. A foundation model, which is a large-scale pre-trained AI model, offers a versatile base that can be adapted to a variety of specific tasks and contexts. Here, we present VIsualization and Segmentation Masked AutoEncoder (VIS-MAE), novel model weights specifically designed for medical imaging. Specifically, VIS-MAE is trained on a dataset of 2.5 million unlabeled images from various modalities (CT, MR, PET,X-rays, and ultrasound), using self-supervised learning techniques. It is then adapted to classification and segmentation tasks using explicit labels. VIS-MAE has high label efficiency, outperforming several benchmark models in both in-domain and out-of-domain applications. In addition, VIS-MAE has improved label efficiency as it can achieve similar performance to other models with a reduced amount of labeled training data (50% or 80%) compared to other pre-trained weights. VIS-MAE represents a significant advancement in medical imaging AI, offering a generalizable and robust solution for improving segmentation and classification tasks while reducing the data annotation workload. The source code of this work is available at https://github.com/lzl199704/VIS-MAE.
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F3-Net: Foundation Model for Full Abnormality Segmentation of Medical Images with Flexible Input Modality Requirement
F3-Net combines multi-encoder nnU-Net with zero-filled missing modalities to segment glioma, metastasis, stroke, and white matter lesions, but the missing-modality claim is untested and comparisons are incomplete.