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Network alignment (NA) is a computational methodology employed to compare biological networks across different species or conditions. By identifying conserved structures, functions, and interactions, NA provides invaluable insights into shared biological processes, evolutionary relationships, and system-level behaviors. This manuscript presents a comprehensive overview of NA methodologies, including the importance of preprocessing network data, selecting suitable input formats, and understanding diverse network types such as attributed, temporal, and multilayer networks. Additionally, it explores key challenges such as seed nodes selection, algorithm configuration, and cross-species alignment, emphasizing the necessity of integrating functional annotations, sequence similarity, and network topology for biologically meaningful results. Various NA strategies, including Local and Global Network Alignment, are discussed alongside their respective advantages and limitations. Practical recommendations for effectively documenting and visualizing NA experiments are also provided, ensuring reproducibility and clarity in research. By leveraging diverse alignment tools and adopting best practices, researchers can unlock the potential of NA to advance our understanding of complex biological systems.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12410751 | PMC |
http://dx.doi.org/10.1371/journal.pcbi.1013386 | DOI Listing |
JMIR Ment Health
September 2025
National Institute of Health and Care Research MindTech HealthTech Research Centre, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
Background: Cross-sector collaboration is increasingly recognized as essential for addressing complex health challenges, including those in mental health. Industry-academic partnerships play a vital role in advancing research and developing health solutions, yet differing priorities and perspectives can make collaboration complex.
Objective: This study aimed to identify key principles to support effective industry-academic partnerships, from the perspective of industry partners, and develop this into actionable guidance, which can be applied across sectors.
Mol Omics
September 2025
Laboratory of Structural Bioinformatics and Computational Biology, Federal University of Rio Grande do Sul, Av. Bento Gonçalves, 9500, Porto Alegre 91501-970, RS, Brazil.
The integration of multimodal single-cell omics data is a state-of-art strategy for deciphering cellular heterogeneity and gene regulatory mechanisms. Recent advances in single-cell technologies have enabled the comprehensive characterization of cellular states and their interactions. However, integrating these high-dimensional and heterogeneous datasets poses significant computational challenges, including batch effects, sparsity, and modality alignment.
View Article and Find Full Text PDFIEEE Trans Neural Netw Learn Syst
September 2025
In multiagent systems, learning optimal behavior policies for individual agents remains a challenging yet crucial task. While recent research has made strides in this area, the issue of when agents should maintain consistent behaviors with one another is still not adequately addressed. This article proposes a novel approach to enable agents to autonomously decide whether their behaviors should align with those of their peers by leveraging intrinsic rewards to optimize their policies.
View Article and Find Full Text PDFIEEE Trans Comput Biol Bioinform
September 2025
The rapid advancement of single-cell sequencing technology has generated vast amounts of multi-omics data, presenting unprecedented opportunities for single-cell multi-omics clustering analysis. However, existing single-cell clustering algorithms focus on extracting shared representations, overlooking the interactions and correlations among cells. This oversight inevitably leads to biased or confounded cell clustering results.
View Article and Find Full Text PDFIEEE J Biomed Health Inform
September 2025
The tumor microenvironment is a dynamic eco system where cellular interactions drive cancer progression. However, inferring cell-cell communication from non-spatial scRNA-seq data remains challenging due to incomplete li gand-receptor databases and noisy cell type annotations. H ere, we propose scGraphDap, a graph neural network frame work that integrates functional state pseudo-labels and graph structure learning to improve both cell type annotation an d CCC inference.
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