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Nettey L, Zheng HB, Devlin JC, et al. Divergent T Cell Phenotypes Define Pediatric Crohn’s Disease and Ulcerative Colitis. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.10.16.25336112

Sy M, Baudi I, Ndiaye IM, et al. SARS-CoV-2 Serosurveillance Reveals Pre-pandemic Cross-Reactivity and Pandemic Seroprevalence Trends in Senegal. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.10.20.25337295

Wang FL, Maher D, Bustamante D, Bountress KE. Symptoms of problematic alcohol use differ in their genetic associations with comorbid internalizing, externalizing, and neurodevelopmental psychiatric disorders. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.10.20.25336759

Hu J, Qin Q, Li H, Zhou Y. FuFiHLA: A tool for Full-Field HLA typing from long reads data. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.23.684216

White S, Liao Y, Burton EM, Asara JM, Gewurz BE. Arginine Metabolism Supports Pyrimidine Biosynthesis to Block DNA Damage and Maintain Epstein-Barr Virus Latency. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.21.683727

Metzl-Raz E, Zhao R, Deshpande S, et al. Deep learning the dynamic regulatory sequence code of cardiac organoid differentiation. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.15.680997

Lian Y, Kotobelli K, Glisic K, et al. Mortality of individuals with antemortem genetic testing for variants in the United States, 1998-2024. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.10.03.25337271

Rühlemann M, Szánthó LL, Waschina S, et al. Convergent genomic responses of human gut bacteria to variations in industrialization. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.20.683395

Garimella K V, Li Q, Wertz J, et al. Population-scale Long-read Sequencing in the Research Program. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.10.02.25336942

Ha YJJ, Maziec D, Markowski J, et al. Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.13.681545