Yonghao Li

Yujie Li, Guannan Lai, Xin Yang et al.

Open-World Continual Learning (OWCL) is a challenging paradigm where models must incrementally learn new knowledge without forgetting while operating under an open-world assumption. This requires handling incomplete training data and recognizing unknown samples during inference. However, existing OWCL methods often treat open detection and continual learning as separate tasks, limiting their ability to integrate open-set detection and incremental classification in OWCL. Moreover, current approaches primarily focus on transferring knowledge from known samples, neglecting the insights derived from unknown/open samples. To address these limitations, we formalize four distinct OWCL scenarios and conduct comprehensive empirical experiments to explore potential challenges in OWCL. Our findings reveal a significant interplay between the open detection of unknowns and incremental classification of knowns, challenging a widely held assumption that unknown detection and known classification are orthogonal processes. Building on our insights, we propose \textbf{HoliTrans} (Holistic Knowns-Unknowns Knowledge Transfer), a novel OWCL framework that integrates nonlinear random projection (NRP) to create a more linearly separable embedding space and distribution-aware prototypes (DAPs) to construct an adaptive knowledge space. Particularly, our HoliTrans effectively supports knowledge transfer for both known and unknown samples while dynamically updating representations of open samples during OWCL. Extensive experiments across various OWCL scenarios demonstrate that HoliTrans outperforms 22 competitive baselines, bridging the gap between OWCL theory and practice and providing a robust, scalable framework for advancing open-world learning paradigms.

Yiran Wei, Yonghao Li, Xi Chen et al.

Glioma is a common malignant brain tumor with distinct survival among patients. The isocitrate dehydrogenase (IDH) gene mutation provides critical diagnostic and prognostic value for glioma. It is of crucial significance to non-invasively predict IDH mutation based on pre-treatment MRI. Machine learning/deep learning models show reasonable performance in predicting IDH mutation using MRI. However, most models neglect the systematic brain alterations caused by tumor invasion, where widespread infiltration along white matter tracts is a hallmark of glioma. Structural brain network provides an effective tool to characterize brain organisation, which could be captured by the graph neural networks (GNN) to more accurately predict IDH mutation. Here we propose a method to predict IDH mutation using GNN, based on the structural brain network of patients. Specifically, we firstly construct a network template of healthy subjects, consisting of atlases of edges (white matter tracts) and nodes (cortical/subcortical brain regions) to provide regions of interest (ROIs). Next, we employ autoencoders to extract the latent multi-modal MRI features from the ROIs of edges and nodes in patients, to train a GNN architecture for predicting IDH mutation. The results show that the proposed method outperforms the baseline models using the 3D-CNN and 3D-DenseNet. In addition, model interpretation suggests its ability to identify the tracts infiltrated by tumor, corresponding to clinical prior knowledge. In conclusion, integrating brain networks with GNN offers a new avenue to study brain lesions using computational neuroscience and computer vision approaches.