Jaiswal S, Natarajan P, Silver AJ, et al. Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease. N Engl J Med. 2017;377(2):111-121. doi:10.1056/NEJMoa1701719
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
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
Lareau CA, Aryee MJ. diffloop: a computational framework for identifying and analyzing differential DNA loops from sequencing data. Bioinformatics. 2018;34(4):672-674. doi:10.1093/bioinformatics/btx623
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
Schneider VA, Graves-Lindsay T, Howe K, et al. Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly. Genome Res. 2017;27(5):849-864. doi:10.1101/gr.213611.116
Cassa CA, Weghorn D, Balick DJ, et al. Estimating the selective effects of heterozygous protein-truncating variants from human exome data. Nat Genet. 2017;49(5):806-810. doi:10.1038/ng.3831