Joshi PK, Esko T, Mattsson H, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 2015;523(7561):459-62. doi:10.1038/nature14618
Mathieson I, Lazaridis I, Rohland N, et al. Genome-wide patterns of selection in 230 ancient Eurasians. Nature. 2015;528(7583):499-503. doi:10.1038/nature16152
Zheng S, Cherniack AD, Dewal N, et al. Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma. Cancer Cell. 2016;29(5):723-36. doi:10.1016/j.ccell.2016.04.002
Batzoglou S, Jaffe DB, Stanley K, et al. ARACHNE: a whole-genome shotgun assembler. Genome Res. 2002;12(1):177-89. doi:10.1101/gr.208902
MacMurray AJ, Weaver A, Shin HS, Lander ES. An automated method for DNA preparation from thousands of YAC clones. Nucleic Acids Res. 1991;19(2):385-90.
Fraser HB, Xie X. Common polymorphic transcript variation in human disease. Genome Res. 2009;19(4):567-75. doi:10.1101/gr.083477.108
International Multiple Sclerosis Genetics Consortium, Hafler DA, Compston A, et al. Risk alleles for multiple sclerosis identified by a genomewide study. N Engl J Med. 2007;357(9):851-62. doi:10.1056/NEJMoa073493
Kamal M, Xie X, Lander ES. A large family of ancient repeat elements in the human genome is under strong selection. Proc Natl Acad Sci U S A. 2006;103(8):2740-5. doi:10.1073/pnas.0511238103
Vitti JJ, Cho MK, Tishkoff SA, Sabeti PC. Human evolutionary genomics: ethical and interpretive issues. Trends Genet. 2012;28(3):137-45. doi:10.1016/j.tig.2011.12.001
Cibulskis K, Lawrence MS, Carter SL, et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol. 2013;31(3):213-9. doi:10.1038/nbt.2514