Feng F, Moran S, Hansen AS, Zhang X, Liu J. Statistically rigorous and computationally efficient chromatin stripe detection with Quagga. Genome research. 2025. doi:10.1101/gr.280132.124
Publications
Yang Q, Wang Y, Sanchez LAC, et al. The PIK3CA/AKT pathway drives therapy resistance in rhabdomyosarcoma. Nature communications. 2025. doi:10.1038/s41467-025-66632-9
Meisel JD, Joshi PR, Spelbring AN, et al. Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency. Nature. 2025. doi:10.1038/s41586-025-09821-2
Grotzinger AD, Werme J, Peyrot WJ, et al. Mapping the genetic landscape across 14 psychiatric disorders. Nature. 2025. doi:10.1038/s41586-025-09820-3
Aliee H, Bejarano-Bosque L, Castells-Graells R, et al. The 2025 generation. Nature cancer. 2025. doi:10.1038/s43018-025-01086-y
Pacheco MP, Gerard D, Mangan RJ, et al. Epigenetic control of metabolic identity across cell types. BMC genomics. 2025. doi:10.1186/s12864-025-12155-y
Wang S, Li T, Naish M, et al. CDCA7 facilitates MET1-mediated CG DNA methylation maintenance in centromeric heterochromatin via linker histone H1. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(50):e2526408122. doi:10.1073/pnas.2526408122
Kurganov E, Cui L, Budnik N, et al. Characterization of the functional and clinical impacts of missense variants found in neurodevelopmental disorders. Science translational medicine. 2025;17(828):eadr0024. doi:10.1126/scitranslmed.adr0024
Rath SP, Mootha VK. The proton motive force maintains mtDNA euploidy by balancing mtDNA replication with cell proliferation. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.27.684790
PMCID
PMC12636550
Zhang Y, Qu H, Qin Q, Li H, Park PJ. Diploid donor-specific assembly enhances somatic structural variant detection in cancer genomes. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.10.28.685155
PMCID
PMC12636593