Hanna RE, Doench JG. A case of mistaken identity. Nat Biotechnol. 2018;36(9):802-804. doi:10.1038/nbt.4208
Genetti CA, Schwartz TS, Robinson JO, et al. Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project. Genet Med. 2019;21(3):622-630. doi:10.1038/s41436-018-0105-6
Bellmunt J, Lalani AKA, 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
Tayoun ANA, Pesaran T, DiStefano MT, et al. Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion. Hum Mutat. 2018;39(11):1517-1524. doi:10.1002/humu.23626
Tolonen AC, Xavier RJ. Dissecting the human microbiome with single-cell genomics. Genome Med. 2017;9(1):56. doi:10.1186/s13073-017-0448-7
Tachmazidou I, Süveges D, Min JL, et al. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Am J Hum Genet. 2017;100(6):865-884. doi:10.1016/j.ajhg.2017.04.014
Akil H, Brenner S, Kandel E, et al. Medicine. The future of psychiatric research: genomes and neural circuits. Science. 2010;327(5973):1580-1. doi:10.1126/science.1188654
Okagaki LH, Nunes CC, Sailsbery J, et al. Genome Sequences of Three Phytopathogenic Species of the Magnaporthaceae Family of Fungi. G3 (Bethesda). 2015;5(12):2539-45. doi:10.1534/g3.115.020057
Meyer M, Palkopoulou E, Baleka S, et al. Palaeogenomes of Eurasian straight-tusked elephants challenge the current view of elephant evolution. Elife. 2017;6. doi:10.7554/eLife.25413
Schäfer M, Klein HU, Schwender H. Integrative analysis of multiple genomic variables using a hierarchical Bayesian model. Bioinformatics. 2017;33(20):3220-3227. doi:10.1093/bioinformatics/btx356