Conway JR, Gillani R, Crowdis J, et al. Somatic structural variants drive distinct modes of oncogenesis in melanoma. The Journal of clinical investigation. 2024;134(13). doi:10.1172/JCI177270
Publications
Conway JR, Gillani R, Crowdis J, et al. Somatic structural variants drive distinct modes of oncogenesis in melanoma. The Journal of clinical investigation. 2024;134(13). doi:10.1172/JCI177270
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Li Y, Ma K, Dong Z, et al. Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models. The Journal of clinical investigation. 2024;134(12). doi:10.1172/JCI177172
Riendeau JM, Gillette AA, Guzman EC, et al. Cellpose as a reliable method for single-cell segmentation of autofluorescence microscopy images. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.07.597994
Gudmundsson S, Singer-Berk M, Stenton SL, et al. Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.593113
Gudmundsson S, Singer-Berk M, Stenton SL, et al. Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.593113