Abstract:Expanding the receptive field in a deep learning model for large-scale 3D point cloud segmentation is an effective technique for capturing rich contextual information, which consequently enhances the network's ability to learn meaningful features. However, this often leads to increased computational complexity and risk of overfitting, challenging the efficiency and effectiveness of the learning paradigm. To address these limitations, we propose the Local Split Attention Pooling (LSAP) mechanism to effectively expand the receptive field through a series of local split operations, thus facilitating the acquisition of broader contextual knowledge. Concurrently, it optimizes the computational workload associated with attention-pooling layers to ensure a more streamlined processing workflow. Based on LSAP, a Parallel Aggregation Enhancement (PAE) module is introduced to enable parallel processing of data using both 2D and 3D neighboring information to further enhance contextual representations within the network. In light of the aforementioned designs, we put forth a novel framework, designated as LSNet, for large-scale point cloud semantic segmentation. Extensive evaluations demonstrated the efficacy of seamlessly integrating the proposed PAE module into existing frameworks, yielding significant improvements in mean intersection over union (mIoU) metrics, with a notable increase of up to 11%. Furthermore, LSNet demonstrated superior performance compared to state-of-the-art semantic segmentation networks on three benchmark datasets, including S3DIS, Toronto3D, and SensatUrban. It is noteworthy that our method achieved a substantial speedup of approximately 38.8% compared to those employing similar-sized receptive fields, which serves to highlight both its computational efficiency and practical utility in real-world large-scale scenes.
Abstract:The accelerated proliferation of visual content and the rapid development of machine vision technologies bring significant challenges in delivering visual data on a gigantic scale, which shall be effectively represented to satisfy both human and machine requirements. In this work, we investigate how hierarchical representations derived from the advanced generative prior facilitate constructing an efficient scalable coding paradigm for human-machine collaborative vision. Our key insight is that by exploiting the StyleGAN prior, we can learn three-layered representations encoding hierarchical semantics, which are elaborately designed into the basic, middle, and enhanced layers, supporting machine intelligence and human visual perception in a progressive fashion. With the aim of achieving efficient compression, we propose the layer-wise scalable entropy transformer to reduce the redundancy between layers. Based on the multi-task scalable rate-distortion objective, the proposed scheme is jointly optimized to achieve optimal machine analysis performance, human perception experience, and compression ratio. We validate the proposed paradigm's feasibility in face image compression. Extensive qualitative and quantitative experimental results demonstrate the superiority of the proposed paradigm over the latest compression standard Versatile Video Coding (VVC) in terms of both machine analysis as well as human perception at extremely low bitrates ($<0.01$ bpp), offering new insights for human-machine collaborative compression.
Abstract:Accurate identification of disease genes has consistently been one of the keys to decoding a disease's molecular mechanism. Most current approaches focus on constructing biological networks and utilizing machine learning, especially, deep learning to identify disease genes, but ignore the complex relations between entities in the biological knowledge graph. In this paper, we construct a biological knowledge graph centered on diseases and genes, and develop an end-to-end Knowledge graph completion model for Disease Gene Prediction using interactional tensor decomposition (called KDGene). KDGene introduces an interaction module between the embeddings of entities and relations to tensor decomposition, which can effectively enhance the information interaction in biological knowledge. Experimental results show that KDGene significantly outperforms state-of-the-art algorithms. Furthermore, the comprehensive biological analysis of the case of diabetes mellitus confirms KDGene's ability for identifying new and accurate candidate genes. This work proposes a scalable knowledge graph completion framework to identify disease candidate genes, from which the results are promising to provide valuable references for further wet experiments.