Background: Glioblastoma multiforme (GBM) is the most common aggressive malignant brain tumor. However, the molecular mechanism of glioblastoma formation is still poorly understood. To identify candidate genes that may be connected to glioma growth and development, weighted gene co-expression network analysis (WGCNA) was performed to construct a gene co-expression network between gene sets and clinical characteristics. We also explored the function of the key candidate gene. Methods: Two GBM datasets were selected from GEO Datasets. The R language was used to identify differentially expressed genes. WGCNA was performed to construct a gene co-expression network in the GEO glioblastoma samples. A custom Venn diagram website was used to find the intersecting genes. The GEPIA website was applied for survival analysis to determine the significant gene, FUBP3. OS, DSS, and PFI analyses, based on the UCSC Cancer Genomics Browser, were performed to verify the significance of FUBP3. Immunohistochemistry was performed to evaluate the expression of FUBP3 in glioblastoma and adjacent normal tissue. KEGG and GO enrichment analyses were used to reveal possible functions of FUBP3. Microenvironment analysis was used to explore the relationship between FUBP3 and immune infiltration. Immunohistochemistry was performed to verify the results of the microenvironment analysis. Results: GSE70231 and GSE108474 were selected from GEO Datasets, then 715 and 694 differentially expressed genes (DEGs) from GSE70231 and GSE108474, respectively, were identified. We then performed weighted gene co-expression network analysis (WGCNA) and identified the most downregulated gene modules of GSE70231 and GSE108474, and 659 and 3915 module genes from GSE70231 and GSE108474, respectively, were selected. Five intersection genes (FUBP3, DAD1, CLIC1, ABR, and DNM1) were calculated by Venn diagram. FUBP3 was then identified as the only significant gene by survival analysis using the GEPIA website. OS, DSS, and PFI analyses verified the significance of FUBP3. Immunohistochemical analysis revealed FUBP3 expression in GBM and adjacent normal tissue. KEGG and GO analyses uncovered the possible function of FUBP3 in GBM. Tumor microenvironment analysis showed that FUBP3 may be connected to immune infiltration, and immunohistochemistry identified a positive correlation between immune cells (CD4 + T cells, CD8 + T cells, and macrophages) and FUBP3. Conclusion: FUBP3 is associated with immune surveillance in GBM, indicating that it has a great impact on GBM development and progression. Therefore, interventions involving FUBP3 and its regulatory pathway may be a new approach for GBM treatment.

We propose a novel discriminative learning approach for Bayesian pattern classification, called ‘constrained maximum margin (CMM)’. We define t

Background/Objectives: Accurate sleep stage classification is essential for evaluating sleep quality and diagnosing sleep disorders. Despite recent advances in deep learning, existing models inadequately represent complex brain dynamics, particularly the time-lag effects inherent in neural signal propagation and regional variations in cortical activation patterns. Methods: We propose the MFST-GCN, a graph-based deep learning framework that models these neurobiological phenomena through three complementary modules. The Dynamic Dual-Scale Functional Connectivity Modeling (DDFCM) module constructs time-varying adjacency matrices using Pearson correlation across 1 s and 5 s windows, capturing both transient signal transmission and sustained connectivity states. This dual-scale approach reflects the biological reality that neural information propagates with measurable delays across brain regions. The Multi-Scale Morphological Feature Extraction Network (MMFEN) employs parallel convolutional branches with varying kernel sizes to extract frequency-specific features corresponding to different EEG rhythms, addressing regional heterogeneity in neural activation. The Adaptive Spatio-Temporal Graph Convolutional Network (ASTGCN) integrates spatial and temporal features through Chebyshev graph convolutions with attention mechanisms, encoding evolving functional dependencies across sleep stages. Results: Evaluation on ISRUC-S1 and ISRUC-S3 datasets demonstrates F1-scores of 0.823 and 0.835, respectively, outperforming state-of-the-art methods. Conclusions: Ablation studies confirm that explicit time-lag modeling contributes substantially to performance gains, particularly in discriminating transitional sleep stages.

Based on Weibo big data, BERTopic, and dual-channel sentiment analysis model, a dynamic analysis framework of public perception and emotion evolution is constructed from the perspective of disaster chain and public response. The results show that (1) Due to the trust of information sources by the public, the efficiency of early warning information reaching the public and attracting attention is relatively high. Social media activity on related topics peaked several times in response to reports of major hazards, such as railway suspensions, passengers trapped in trains, and severe flooding in Miyun District, Beijing. (2) The evolution of topics of public attention strongly corresponds to the disaster process: From early warning and emergency risk avoidance, gradually move to disaster report and rescue coordination, and finally focus on the criticism of infrastructure vulnerability. (3) The emotional response presents phased characteristics. At the initial stage of the rainstorm red warning issued by the meteorological department, anxiety is dominant; after the release of rescue information, emotion rises briefly, and reflection and attribution tendencies generally appear after the disaster. (4) Elderly populations and those in remote areas exhibit characteristics of vulnerability, information isolation, and high dependency in response to disasters.