98%
921
2 minutes
20
High-dimensional single-cell data analysis is crucial for understanding complex biological interactions, yet conventional dimensionality reduction methods (DRMs) often fail to preserve both global and local structures. Existing DRMs, such as t-distributed Stochastic Neighbor Embedding (t-SNE), Uniform Manifold Approximation and Projection (UMAP), Principal Component Analysis (PCA), and Potential of Heat-diffusion for Affinity-based Transition Embedding (PHATE), optimize different visualization objectives, resulting in trade-offs between cluster separability, spatial organization, and temporal coherence. To overcome these limitations, we introduce GIBOOST, an AI-driven framework that integrates outputs from multiple DRMs using a Bayesian framework and an optimized autoencoder. GIBOOST systematically selects and integrates the two most informative DRMs by evaluating key visualization features, including separability, spatial continuity, uniformity, cellular dynamics, and cluster sensitivity. Rather than prioritizing a single DRM, it identifies the optimal combination that maximizes clustering sensitivity (GI) while preserving biologically relevant spatial and temporal structures. This integration is further refined through a GI-optimized autoencoder, which optimizes the joint distribution of GI, neuron count, and batch size effects to improve visualization quality. We demonstrate GIBOOST's efficacy across multiple dynamic biological processes, including epithelial-mesenchymal transition, CiPSC reprogramming, spermatogenesis, and placental development. Compared to nine individual DRMs, GIBOOST enhances clustering sensitivity and biological relevance by ~30%, enabling more accurate interpretation of differentiation trajectories and cell-cell interactions. When applied to a large single-cell RNA-seq dataset (~400 000 cells, 28 cell types, seven placental regions), GIBOOST uncovers novel immune-placenta interactions, providing deeper insights into cross-tissue communication during pregnancy. By improving both the visualization and interpretability of high-dimensional data, GIBOOST serves as a powerful tool for computational systems biology, enabling a more accurate exploration of complex cellular systems.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371410 | PMC |
http://dx.doi.org/10.1093/bib/bbaf415 | DOI Listing |
Phys Rev Lett
August 2025
The University of Tokyo, Research Center for Advanced Science and Technology, 4-6-1 Komaba, Meguro, Tokyo 153-8904, Japan.
Hopfions-higher-dimensional topological quasiparticles with sophisticated 3D knotted spin textures discovered in condensed matter and photonic systems-show promise in high-density data storage and transfer. Here, we present crystalline structures of hopfions lying in space-time constructed by spatiotemporally structured light. Practical methodologies using bichromatic structured light beams or dipole arrays to assemble 1D and higher dimensional hopfion lattices are proposed, and a technique for tailoring topological orders is elucidated.
View Article and Find Full Text PDFAm J Physiol Cell Physiol
September 2025
Department of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC.
Cachexia, the loss of skeletal muscle mass and function with cancer, contributes to reduced life quality and worsened survival. Skeletal muscle fibrosis leads to disproportionate muscle weakness; however, the role of infiltrating immune cells and fibro-adipogenic progenitors (FAPs) in cancer-induced muscle fibrosis is not well understood. Using the C26 model of cancer cachexia, we sought to examine the changes to skeletal muscle immune cells and FAPs which contribute to excessive extracellular matrix (ECM) collagen deposition.
View Article and Find Full Text PDFBioinformatics
September 2025
The Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Motivation: Drug repositioning presents a streamlined and cost-efficient way to expand the range of therapeutic possibilities. Drugs with human genetic evidence are more likely to advance successfully through clinical trials towards FDA approval. Single gene-based drug repositioning methods have been implemented, but approaches leveraging a broad spectrum of molecular signatures remain underexplored.
View Article and Find Full Text PDFBioinformatics
September 2025
Department of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania United States.
Summary: Causal mediation analysis investigates the role of mediators in the relationship between exposure and outcome. In the analysis of omics or imaging data, mediators are often high-dimensional, presenting challenges such as multicollinearity and interpretability. Existing methods either compromise interpretability or fail to effectively prioritize mediators.
View Article and Find Full Text PDFMol 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 PDF