DSKCA-UNet: Dynamic selective kernel channel attention for medical image segmentation.

U-Net has attained immense popularity owing to its performance in medical image segmentation. However, it cannot be modeled explicitly over remote dependencies. By contrast, the transformer can effectively capture remote dependencies by leveraging the self-attention (SA) of the encoder. Although SA, an important characteristic of the transformer, can find correlations between them based on the original data, secondary computational complexity might retard the processing rate of high-dimensional data (such as medical images). Furthermore, SA is limited because the correlation between samples is overlooked; thus, there is considerable scope for improvement. To this end, based on Swin-UNet, we introduce a dynamic selective attention mechanism for the convolution kernels. The weight of each convolution kernel is calculated to fuse the results dynamically. This attention mechanism permits each neuron to adaptively modify its receptive field size in response to multiscale input information. A local cross-channel interaction strategy without dimensionality reduction was introduced, which effectively eliminated the influence of downscaling on learning channel attention. Through suitable cross-channel interactions, model complexity can be significantly reduced while maintaining its performance. Subsequently, the global interaction between the encoder features is used to extract more fine-grained features. Simultaneously, the mixed loss function of the weighted cross-entropy loss and Dice loss is used to alleviate category imbalances and achieve better results when the sample number is unbalanced. We evaluated our proposed method on abdominal multiorgan segmentation and cardiac segmentation datasets, achieving Dice similarity coefficient and 95% Hausdorff distance metrics of 80.30 and 14.55%, respectively, on the Synapse dataset and Dice similarity coefficient metrics of 90.80 on the ACDC dataset. The experimental results show that our proposed method has good generalization ability and robustness, and it is a powerful tool for medical image segmentation.

Feature interaction network based on hierarchical decoupled convolution for 3D medical image segmentation.

Manual image segmentation consumes time. An automatic and accurate method to segment multimodal brain tumors using context information rich three-dimensional medical images that can be used for clinical treatment decisions and surgical planning is required. However, it is a challenge to use deep learning to achieve accurate segmentation of medical images due to the diversity of tumors and the complex boundary interactions between sub-regions while limited computing resources hinder the construction of efficient neural networks. We propose a feature fusion module based on a hierarchical decoupling convolution network and an attention mechanism to improve the performance of network segmentation. We replaced the skip connections of U-shaped networks with a feature fusion module to solve the category imbalance problem, thus contributing to the segmentation of more complicated medical images. We introduced a global attention mechanism to further integrate the features learned by the encoder and explore the context information. The proposed method was evaluated for enhance tumor, whole tumor, and tumor core, achieving Dice similarity coefficient metrics of 0.775, 0.900, and 0.827, respectively, on the BraTS 2019 dataset and 0.800, 0.902, and 0.841, respectively on the BraTS 2018 dataset. The results show that our proposed method is inherently general and is a powerful tool for brain tumor image studies. Our code is available at: https://github.com/WSake/Feature-interaction-network-based-on-Hierarchical-Decoupled-Convolution.

Prediction of RNA secondary structure based on stem region replacement using the RSRNA algorithm.

RNA functions, including the regulation of various cellular activities, seem to be closely related to its structure. However, accurately predicting RNA secondary structures can be difficult. Structural prediction can be achieved by selecting stem areas that are suitable and compatible from stem pools. Here, we propose a method for predicting the secondary structure of non-coding RNA based on stem region substitution, which we named RSRNA. This method is compatible with nested RNA secondary structures, while reducing any randomness. Our algorithm had higher performance and prediction accuracy than other algorithms, which deems it more effective for future RNA structure studies.