SciceVPR: Stable Cross-Image Correlation Enhanced Model for Visual Place Recognition

Visual Place Recognition (VPR) is a major challenge for robotics and autonomous systems, with the goal of predicting the location of an image based solely on its visual features. State-of-the-art (SOTA) models extract global descriptors using the powerful foundation model DINOv2 as backbone. These models either explore the cross-image correlation or propose a time-consuming two-stage re-ranking strategy to achieve better performance. However, existing works only utilize the final output of DINOv2, and the current cross-image correlation causes unstable retrieval results. To produce both discriminative and constant global descriptors, this paper proposes stable cross-image correlation enhanced model for VPR called SciceVPR. This model explores the full potential of DINOv2 in providing useful feature representations that implicitly encode valuable contextual knowledge. Specifically, SciceVPR first uses a multi-layer feature fusion module to capture increasingly detailed task-relevant channel and spatial information from the multi-layer output of DINOv2. Secondly, SciceVPR considers the invariant correlation between images within a batch as valuable knowledge to be distilled into the proposed self-enhanced encoder. In this way, SciceVPR can acquire fairly robust global features regardless of domain shifts (e.g., changes in illumination, weather and viewpoint between pictures taken in the same place). Experimental results demonstrate that the base variant, SciceVPR-B, outperforms SOTA one-stage methods with single input on multiple datasets with varying domain conditions. The large variant, SciceVPR-L, performs on par with SOTA two-stage models, scoring over 3% higher in Recall@1 compared to existing models on the challenging Tokyo24/7 dataset. Our code will be released at https://github.com/shuimushan/SciceVPR.

Optimize transfer learning for lung diseases in bronchoscopy using a new concept: sequential fine-tuning

Bronchoscopy inspection as a follow-up procedure from the radiological imaging plays a key role in lung disease diagnosis and determining treatment plans for the patients. Doctors needs to make a decision whether to biopsy the patients timely when performing bronchoscopy. However, the doctors also needs to be very selective with biopsies as biopsies may cause uncontrollable bleeding of the lung tissue which is life-threaten. To help doctors to be more selective on biopsies and provide a second opinion on diagnosis, in this work, we propose a computer-aided diagnosis (CAD) system for lung diseases including cancers and tuberculosis (TB). The system is developed based on transfer learning. We propose a novel transfer learning method: sentential fine-tuning . Compared to traditional fine-tuning methods, our methods achieves the best performance. We obtained a overall accuracy of 77.0% a dataset of 81 normal cases, 76 tuberculosis cases and 277 lung cancer cases while the other traditional transfer learning methods achieve an accuracy of 73% and 68%. . The detection accuracy of our method for cancers, TB and normal cases are 87%, 54% and 91% respectively. This indicates that the CAD system has potential to improve lung disease diagnosis accuracy in bronchoscopy and it also might be used to be more selective with biopsies.