Mitchell W, Goeminne LJE, Tyshkovskiy A, et al. Multi-omics characterization of partial chemical reprogramming reveals evidence of cell rejuvenation. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.06.30.546730
Publications
Koenig Z, Yohannes MT, Nkambule LL, et al. A harmonized public resource of deeply sequenced diverse human genomes. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.01.23.525248
Barton AR, Santander CG, Skoglund P, Moltke I, Reich D, Mathieson I. Insufficient evidence for natural selection associated with the Black Death. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.14.532615
Shaban M, Bai Y, Qiu H, et al. MAPS: Pathologist-level cell type annotation from tissue images through machine learning. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.06.25.546474
Dunlap G, Wagner A, Meednu N, et al. Clonal associations of lymphocyte subsets and functional states revealed by single cell antigen receptor profiling of T and B cells in rheumatoid arthritis synovium. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.18.533282
Zhou H, Kember RL, Deak JD, et al. Multi-ancestry study of the genetics of problematic alcohol use in >1 million individuals. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.01.24.23284960
Akshay A, Katoch M, Abedi M, et al. SpheroScan: A User-Friendly Deep Learning Tool for Spheroid Image Analysis. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.06.28.533479
Hu Y, Ma S, Kartha VK, et al. Single-cell multi-scale footprinting reveals the modular organization of DNA regulatory elements. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.28.533945
Edelstein GE, Boucau J, Uddin R, et al. SARS-CoV-2 virologic rebound with nirmatrelvir-ritonavir therapy. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.23.23288598
Chen S, Neale BM, Berkovic SF, . Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.02.22.23286310