REVIEW 1 cited by
DAMamba: Vision State Space Model with Dynamic Adaptive Scan
Not yet reviewed by Pith; the record is open.
This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.
SPECIMEN: schema-true, not a live event
T0 review · schema-true
One-sentence machine reading of the paper's core claim.
pith:XXXXXXXX · record.json · timestamp
read the original abstract
State space models (SSMs) have recently garnered significant attention in computer vision. However, due to the unique characteristics of image data, adapting SSMs from natural language processing to computer vision has not outperformed the state-of-the-art convolutional neural networks (CNNs) and Vision Transformers (ViTs). Existing vision SSMs primarily leverage manually designed scans to flatten image patches into sequences locally or globally. This approach disrupts the original semantic spatial adjacency of the image and lacks flexibility, making it difficult to capture complex image structures. To address this limitation, we propose Dynamic Adaptive Scan (DAS), a data-driven method that adaptively allocates scanning orders and regions. This enables more flexible modeling capabilities while maintaining linear computational complexity and global modeling capacity. Based on DAS, we further propose the vision backbone DAMamba, which significantly outperforms current state-of-the-art vision Mamba models in vision tasks such as image classification, object detection, instance segmentation, and semantic segmentation. Notably, it surpasses some of the latest state-of-the-art CNNs and ViTs. Code will be available at https://github.com/ltzovo/DAMamba.
Forward citations
Cited by 1 Pith paper
-
DAMamba-UNet3D: A Parameter-Efficient Mamba State Space U-Net with Dynamic Adaptive Scan for 3D Medical Image Segmentation
DAMamba-UNet3D combines encoder-only tri-plane Dynamic Adaptive Scan with a convolutional U-Net, reaching 0.815 mean Dice on BraTS 2020 at 5.3M parameters.
Discussion (0). Continue with ORCID to comment.