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Dai M, Török T, Sun D, et al. LARIS enables accurate and efficient ligand and receptor interaction analysis in spatial transcriptomics. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.26.690796

Queen O, Huang Y, Calef R, et al. ProCyon: A multimodal foundation model for protein phenotypes. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2024.12.10.627665

Walker AJ, Fisher TM, Caldwell SK, et al. Early-life stromal niches orchestrate B lymphopoiesis at the brain’s borders. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.27.690844

Xie H, Jiang A, Dey A, et al. Lymphotoxin-driven cancer cell eradication by tumoricidal CD8 TIL. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.19.689204

Audam TN, Schmandt B, Huang Y, et al. The Coronary Artery Disease Risk Locus Modulates Vascular Cell-State Transitions via Enhancer-Driven Regulation of . bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.18.689066

Rao I, Kellis M, Tanigawa Y. sc4D: spatio-temporal single-cell transcriptomics analysis through embedded optimal transport identifies joint glial response to Alzheimer’s disease pathology. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.11.19.689166

Kunorozva L, Valliere J, Chen CY, et al. From Normal Variation in Sleep to Clinical Sleep Disorders: Genetic Insights from Over One Million Individuals. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.21.25340447

Sevilla-González M, Wang N, Hanson PA, et al. Dissecting Genetic and Environmental Determinants of Plasma Molecular Signatures and Their Link to Type 2 Diabetes Risk. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.26.25341007

Hirayama S, Al-Inaya Y, Bryan ME, et al. Clinical validation of an HPV whole genome sequencing assay for molecular residual disease detection in HPV-associated head and neck cancer patients treated with surgery. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.24.25340887

Taylor K, Huerta-Chagoya A, Wang X, et al. Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.11.24.25340878