4.7 Article

Adapt Everywhere: Unsupervised Adaptation of Point-Clouds and Entropy Minimization for Multi-Modal Cardiac Image Segmentation

期刊

IEEE TRANSACTIONS ON MEDICAL IMAGING
卷 40, 期 7, 页码 1838-1851

出版社

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TMI.2021.3066683

关键词

Image segmentation; Shape; Entropy; Magnetic resonance imaging; Minimization; Adaptation models; Training; Unsupervised domain adaptation; cardiac segmentation; multi-modal segmentation; adversarial learning; point-clouds; entropy minimization

资金

  1. Project EFI-BIG-THERA: Integrative BigData Modeling

向作者/读者索取更多资源

Deep learning models are sensitive to domain shift phenomena, where data distribution differs between source and target domains. Unsupervised domain adaptation methods aim to reduce this gap, but may show degraded performance with insufficient data.
Deep learning models are sensitive to domain shift phenomena. A model trained on images from one domain cannot generalise well when tested on images from a different domain, despite capturing similar anatomical structures. It is mainly because the data distribution between the two domains is different. Moreover, creating annotation for every new modality is a tedious and time-consuming task, which also suffers from high inter- and intra- observer variability. Unsupervised domain adaptation (UDA) methods intend to reduce the gap between source and target domains by leveraging source domain labelled data to generate labels for the target domain. However, current state-of-the-art (SOTA) UDA methods demonstrate degraded performance when there is insufficient data in source and target domains. In this paper, we present a novel UDA method for multi-modal cardiac image segmentation. The proposed method is based on adversarial learning and adapts network features between source and target domain in different spaces. The paper introduces an end-to-end framework that integrates: a) entropy minimization, b) output feature space alignment and c) a novel point-cloud shape adaptation based on the latent features learned by the segmentation model. We validated our method on two cardiac datasets by adapting from the annotated source domain, bSSFP-MRI (balanced Steady-State Free Procession-MRI), to the unannotated target domain, LGE-MRI (Late-gadolinium enhance-MRI), for the multi-sequence dataset; and from MRI (source) to CT (target) for the cross-modality dataset. The results highlighted that by enforcing adversarial learning in different parts of the network, the proposed method delivered promising performance, compared to other SOTA methods.

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