1.
Currall BB, Antolik CW, Collins RL, Talkowski ME. Next Generation Sequencing of Prenatal Structural Chromosomal Rearrangements Using Large-Insert Libraries. Methods Mol Biol. 2019;1885:251-265. doi:10.1007/978-1-4939-8889-1_17.
1.
Brody Y, Kimmerling RJ, Maruvka YE, et al. Quantification of somatic mutation flow across individual cell division events by lineage sequencing. Genome Res. 2018;28(12):1901-1918. doi:10.1101/gr.238543.118.
1.
Iqbal NS, Jascur TA, Harrison S, et al. Copy number variations in a population with prune belly syndrome. Am J Med Genet A. 2018;176(11):2276-2283. doi:10.1002/ajmg.a.40476.
1.
Jabbari K, Bobbili DR, Lal D, et al. Rare gene deletions in genetic generalized and Rolandic epilepsies. PLoS One. 2018;13(8):e0202022. doi:10.1371/journal.pone.0202022.
1.
Tan L, Xing D, Chang C-H, Li H, Xie S. Three-dimensional genome structures of single diploid human cells. Science. 2018;361(6405):924-928. doi:10.1126/science.aat5641.
1.
Bellmunt J, Lalani A-KA, Jacobus S, et al. Everolimus and pazopanib (E/P) benefit genomically selected patients with metastatic urothelial carcinoma. Br J Cancer. 2018;119(6):707-712. doi:10.1038/s41416-018-0261-0.
1.
Kwong LN, Zou L, Chagani S, et al. Modeling Genomic Instability and Selection Pressure in a Mouse Model of Melanoma. Cell Rep. 2017;19(7):1304-1312. doi:10.1016/j.celrep.2017.04.065.
1.
Abascal F, Juan D, Jungreis I, et al. Loose ends: almost one in five human genes still have unresolved coding status. Nucleic Acids Res. 2018;46(14):7070-7084. doi:10.1093/nar/gky587.
1.
Berger AC, Korkut A, Kanchi RS, et al. A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers. Cancer Cell. 2018;33(4):690-705.e9. doi:10.1016/j.ccell.2018.03.014.
1.
Mei Y, Bi WL, Greenwald NF, et al. Genomic profile of human meningioma cell lines. PLoS One. 2017;12(5):e0178322. doi:10.1371/journal.pone.0178322.