RESUMO
Real-world 3D structured data like point clouds and skeletons often can be represented as data in a 3D rotation group (denoted as [Formula: see text]). However, most existing neural networks are tailored for the data in the euclidean space, which makes the 3D rotation data not closed under their algebraic operations and leads to sub-optimal performance in 3D-related learning tasks. To resolve the issues caused by the above mismatching between data and model, we propose a novel non-real neuron model called quaternion product unit (QPU) to represent data on 3D rotation groups. The proposed QPU leverages quaternion algebra and the law of the 3D rotation group, representing 3D rotation data as quaternions and merging them via a weighted chain of Hamilton products. We demonstrate that the QPU mathematically maintains the [Formula: see text] structure of the 3D rotation data during the inference process and disentangles the 3D representations into "rotation-invariant" features and "rotation-equivariant" features, respectively. Moreover, we design a fast QPU to accelerate the computation of QPU. The fast QPU applies a tree-structured data indexing process, and accordingly, leverages the power of parallel computing, which reduces the computational complexity of QPU in a single thread from O(N) to O(logN). Taking the fast QPU as a basic module, we develop a series of quaternion neural networks (QNNs), including quaternion multi-layer perceptron (QMLP), quaternion message passing (QMP), and so on. In addition, we make the QNNs compatible with conventional real-valued neural networks and applicable for both skeletons and point clouds. Experiments on synthetic and real-world 3D tasks show that the QNNs based on our fast QPUs are superior to state-of-the-art real-valued models, especially in the scenarios requiring the robustness to random rotations. The code of this work is available at https://github.com/SuferQin/Fast-QPU.
RESUMO
Examination of pathological images is the golden standard for diagnosing and screening many kinds of cancers. Multiple datasets, benchmarks, and challenges have been released in recent years, resulting in significant improvements in computer-aided diagnosis (CAD) of related diseases. However, few existing works focus on the digestive system. We released two well-annotated benchmark datasets and organized challenges for the digestive-system pathological cell detection and tissue segmentation, in conjunction with the International Conference on Medical Image Computing and Computer-Assisted Intervention (MICCAI). This paper first introduces the two released datasets, i.e., signet ring cell detection and colonoscopy tissue segmentation, with the descriptions of data collection, annotation, and potential uses. We also report the set-up, evaluation metrics, and top-performing methods and results of two challenge tasks for cell detection and tissue segmentation. In particular, the challenge received 234 effective submissions from 32 participating teams, where top-performing teams developed advancing approaches and tools for the CAD of digestive pathology. To the best of our knowledge, these are the first released publicly available datasets with corresponding challenges for the digestive-system pathological detection and segmentation. The related datasets and results provide new opportunities for the research and application of digestive pathology.
