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A Self-Adaptive Network for Multiple Sclerosis Lesion Segmentation From Multi-Contrast MRI With Various Imaging Sequences

机译:一个自适应网络从多造影剂MRI的各种成像序列的多发性硬化症病变分割。

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Deep neural networks have shown promises in the lesion segmentation of multiple sclerosis (MS) from multi-contrast MRI including T1, T2, PD and FLAIR sequences. However, one challenge in deploying such networks into clinical practice is missing MRI sequences due to the variability of image acquisition protocols. Therefore, trained networks need to adapt to practical situations where specific MRI sequences are unavailable. In this paper, we propose a DNN-based MS lesion segmentation framework with a novel technique called sequence dropout. Without altering network architecture, our method ensured the robustness of the network to missing sequences and could achieve its maximal possible performance from a given set of input sequences.Experiments were performed on the IEEE ISBI 2015 Longitudinal MS Lesion Challenge dataset and our method is currently ranked 2nd with a Dice similarity coefficient of 0.684. Experiments also showed our network achieved its maximal performance with one missing sequence during deployment by comparing with separate networks of the same architecture but trained using the corresponding set of input sequences. Our network achieved a non-inferior performance without re-training. Experiments with multiple missing sequences further showed the robustness of our network. Also, with this framework, we studied the quantitative impact of each MRI sequence on the MS lesion segmentation task without training separate networks.
机译:深度神经网络已在包括T1,T2,PD和FLAIR序列在内的多对比度MRI的多发性硬化症(MS)病变分割中显示出希望。然而,由于图像采集协议的可变性,将这样的网络部署到临床实践中的一个挑战是缺少MRI序列。因此,训练有素的网络需要适应无法使用特定MRI序列的实际情况。在本文中,我们提出了一种基于DNN的MS病变分割框架,该框架具有一种称为序列缺失的新技术。在不更改网络体系结构的情况下,我们的方法确保了网络对丢失序列的鲁棒性,并可以从给定的一组输入序列中实现其最大可能的性能。对IEEE ISBI 2015纵向MS病害挑战数据集进行了实验,目前该方法已排名2个 nd 骰子相似系数为0.684。实验还表明,通过与相同架构但使用相应输入序列集进行训练的单独网络进行比较,我们的网络在部署过程中通过缺少一个序列实现了最佳性能。我们的网络在不进行重新培训的情况下取得了不逊色的性能。多个缺失序列的实验进一步证明了我们网络的鲁棒性。同样,在此框架下,我们无需训练单独的网络就可以研究每个MRI序列对MS病变分割任务的定量影响。

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