The low-rank plus sparse (L+S) decomposition model has enabled better reconstruction of dynamic magnetic resonance imaging (dMRI) with separation into background (L) and dynamic (S) component. However, use of low-rank prior alone may not fully explain the slow variations or smoothness of the background part at the local scale. In this paper, we propose a smoothness-regularized L+S (SR-L+S) model for dMRI reconstruction from highly undersampled k-t-space data. We exploit joint low-rank and smooth priors on the background component of dMRI to better capture both its global and local temporal correlated structures. Extending the L+S formulation, the low-rank property is encoded by the nuclear norm, while the smoothness by a general \ell_{p}-norm penalty on the local differences of the columns of L. The additional smoothness regularizer can promote piecewise local consistency between neighboring frames. By smoothing out the noise and dynamic activities, it allows accurate recovery of the background part, and subsequently more robust dMRI reconstruction. Extensive experiments on multi-coil cardiac and synthetic data shows that the SR-L+S model outp
Medical image semantic segmentation techniques can help identify tumors automatically from computed tomography (CT) scans. In this paper, we propose a Contextual and Attentional feature Fusions enhanced Convolutional Neural Network (CNN) and Transformer hybrid network (CAFCT) model for liver tumor segmentation. In the proposed model, three other modules are introduced in the network architecture: Attentional Feature Fusion (AFF), Atrous Spatial Pyramid Pooling (ASPP) of DeepLabv3, and Attention Gates (AGs) to improve contextual information related to tumor boundaries for accurate segmentation. Experimental results show that the proposed CAFCT achieves a mean Intersection over Union (IoU) of 90.38% and Dice score of 86.78%, respectively, on the Liver Tumor Segmentation Benchmark (LiTS) dataset, outperforming pure CNN or Transformer methods, e.g., Attention U-Net, and PVTFormer.
We propose a novel Attentional Scale Sequence Fusion based You Only Look Once (YOLO) framework (ASF-YOLO) which combines spatial and scale features for accurate and fast cell instance segmentation. Built on the YOLO segmentation framework, we employ the Scale Sequence Feature Fusion (SSFF) module to enhance the multi-scale information extraction capability of the network, and the Triple Feature Encoder (TPE) module to fuse feature maps of different scales to increase detailed information. We further introduce a Channel and Position Attention Mechanism (CPAM) to integrate both the SSFF and TPE modules, which focus on informative channels and spatial position-related small objects for improved detection and segmentation performance. Experimental validations on two cell datasets show remarkable segmentation accuracy and speed of the proposed ASF-YOLO model. It achieves a box mAP of 0.91, mask mAP of 0.887, and an inference speed of 47.3 FPS on the 2018 Data Science Bowl dataset, outperforming the state-of-the-art methods. The source code is available at https://github.com/mkang315/ASF-YOLO.
You Only Look Once (YOLO)-based object detectors have shown remarkable accuracy for automated brain tumor detection. In this paper, we develop a novel BGF-YOLO architecture by incorporating Bi-level Routing Attention (BRA), Generalized feature pyramid networks (GFPN), and Fourth detecting head into YOLOv8. BGF-YOLO contains an attention mechanism to focus more on important features, and feature pyramid networks to enrich feature representation by merging high-level semantic features with spatial details. Furthermore, we investigate the effect of different attention mechanisms and feature fusions, detection head architectures on brain tumor detection accuracy. Experimental results show that BGF-YOLO gives a 4.7% absolute increase of mAP$_{50}$ compared to YOLOv8x, and achieves state-of-the-art on the brain tumor detection dataset Br35H. The code is available at https://github.com/mkang315/BGF-YOLO.
With an excellent balance between speed and accuracy, cutting-edge YOLO frameworks have become one of the most efficient algorithms for object detection. However, the performance of using YOLO networks is scarcely investigated in brain tumor detection. We propose a novel YOLO architecture with Reparameterized Convolution based on channel Shuffle (RCS-YOLO). We present RCS and a One-Shot Aggregation of RCS (RCS-OSA), which link feature cascade and computation efficiency to extract richer information and reduce time consumption. Experimental results on the brain tumor dataset Br35H show that the proposed model surpasses YOLOv6, YOLOv7, and YOLOv8 in speed and accuracy. Notably, compared with YOLOv7, the precision of RCS-YOLO improves by 2.6%, and the inference speed by 60% at 114.8 images detected per second (FPS). Our proposed RCS-YOLO achieves state-of-the-art performance on the brain tumor detection task. The code is available at https://github.com/mkang315/RCS-YOLO.
Blood cell detection is a typical small-scale object detection problem in computer vision. In this paper, we propose a CST-YOLO model for blood cell detection based on YOLOv7 architecture and enhance it with the CNN-Swin Transformer (CST), which is a new attempt at CNN-Transformer fusion. We also introduce three other useful modules: Weighted Efficient Layer Aggregation Networks (W-ELAN), Multiscale Channel Split (MCS), and Concatenate Convolutional Layers (CatConv) in our CST-YOLO to improve small-scale object detection precision. Experimental results show that the proposed CST-YOLO achieves 92.7, 95.6, and 91.1 mAP@0.5 respectively on three blood cell datasets, outperforming state-of-the-art object detectors, e.g., YOLOv5 and YOLOv7. Our code is available at https://github.com/mkang315/CST-YOLO.
Data-driven soft sensors are essential for achieving accurate perception through reliable state inference. However, developing representative soft sensor models is challenged by issues such as missing labels, domain adaptability, and temporal coherence in data. To address these challenges, we propose a deep Particle Flow Bayes (DPFB) framework for cross-domain soft sensor modeling in the absence of target state labels. In particular, a sequential Bayes objective is first formulated to perform the maximum likelihood estimation underlying the cross-domain soft sensing problem. At the core of the framework, we incorporate a physics-inspired particle flow that optimizes the sequential Bayes objective to perform an exact Bayes update of the model extracted latent and hidden features. As a result, these contributions enable the proposed framework to learn a rich approximate posterior feature representation capable of characterizing complex cross-domain system dynamics and performing effective time series unsupervised domain adaptation (UDA). Finally, we validate the framework on a complex industrial multiphase flow process system with complex dynamics and multiple operating conditions. The results demonstrate that the DPFB framework achieves superior cross-domain soft sensing performance, outperforming state-of-the-art deep UDA and normalizing flow approaches.
Recent applications of pattern recognition techniques on brain connectome classification using functional connectivity (FC) neglect the non-Euclidean topology and causal dynamics of brain connectivity across time. In this paper, a deep probabilistic spatiotemporal framework developed based on variational Bayes (DSVB) is proposed to learn time-varying topological structures in dynamic brain FC networks for autism spectrum disorder (ASD) identification. The proposed framework incorporates a spatial-aware recurrent neural network to capture rich spatiotemporal patterns across dynamic FC networks, followed by a fully-connected neural network to exploit these learned patterns for subject-level classification. To overcome model overfitting on limited training datasets, an adversarial training strategy is introduced to learn graph embedding models that generalize well to unseen brain networks. Evaluation on the ABIDE resting-state functional magnetic resonance imaging dataset shows that our proposed framework significantly outperformed state-of-the-art methods in identifying ASD. Dynamic FC analyses with DSVB learned embeddings reveal apparent group difference between ASD and healthy controls in network profiles and switching dynamics of brain states.