Chen Chen

Xianpeng Liu, Ce Zheng, Ming Qian et al.

We present Multi-View Attentive Contextualization (MvACon), a simple yet effective method for improving 2D-to-3D feature lifting in query-based multi-view 3D (MV3D) object detection. Despite remarkable progress witnessed in the field of query-based MV3D object detection, prior art often suffers from either the lack of exploiting high-resolution 2D features in dense attention-based lifting, due to high computational costs, or from insufficiently dense grounding of 3D queries to multi-scale 2D features in sparse attention-based lifting. Our proposed MvACon hits the two birds with one stone using a representationally dense yet computationally sparse attentive feature contextualization scheme that is agnostic to specific 2D-to-3D feature lifting approaches. In experiments, the proposed MvACon is thoroughly tested on the nuScenes benchmark, using both the BEVFormer and its recent 3D deformable attention (DFA3D) variant, as well as the PETR, showing consistent detection performance improvement, especially in enhancing performance in location, orientation, and velocity prediction. It is also tested on the Waymo-mini benchmark using BEVFormer with similar improvement. We qualitatively and quantitatively show that global cluster-based contexts effectively encode dense scene-level contexts for MV3D object detection. The promising results of our proposed MvACon reinforces the adage in computer vision -- ``(contextualized) feature matters".

Xingbo Fu, Chen Chen, Yushun Dong et al.

An antibiogram is a periodic summary of antibiotic resistance results of organisms from infected patients to selected antimicrobial drugs. Antibiograms help clinicians to understand regional resistance rates and select appropriate antibiotics in prescriptions. In practice, significant combinations of antibiotic resistance may appear in different antibiograms, forming antibiogram patterns. Such patterns may imply the prevalence of some infectious diseases in certain regions. Thus it is of crucial importance to monitor antibiotic resistance trends and track the spread of multi-drug resistant organisms. In this paper, we propose a novel problem of antibiogram pattern prediction that aims to predict which patterns will appear in the future. Despite its importance, tackling this problem encounters a series of challenges and has not yet been explored in the literature. First of all, antibiogram patterns are not i.i.d as they may have strong relations with each other due to genomic similarities of the underlying organisms. Second, antibiogram patterns are often temporally dependent on the ones that are previously detected. Furthermore, the spread of antibiotic resistance can be significantly influenced by nearby or similar regions. To address the above challenges, we propose a novel Spatial-Temporal Antibiogram Pattern Prediction framework, STAPP, that can effectively leverage the pattern correlations and exploit the temporal and spatial information. We conduct extensive experiments on a real-world dataset with antibiogram reports of patients from 1999 to 2012 for 203 cities in the United States. The experimental results show the superiority of STAPP against several competitive baselines.