Crompton BD, Stewart C, Taylor-Weiner A, et al. The genomic landscape of pediatric Ewing sarcoma. Cancer Discov. 2014;4(11):1326-41. doi:10.1158/2159-8290.CD-13-1037
Ramos AH, Lichtenstein L, Gupta M, et al. Oncotator: cancer variant annotation tool. Hum Mutat. 2015;36(4):E2423-9. doi:10.1002/humu.22771
Shirts BH, Salama JS, Aronson SJ, et al. CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record. J Am Med Inform Assoc. 2015;22(6):1231-42. doi:10.1093/jamia/ocv065
Chain PSG, Grafham DV, Fulton RS, et al. Genomics. Genome project standards in a new era of sequencing. Science. 2009;326(5950):236-7. doi:10.1126/science.1180614
Hoy MA, Waterhouse RM, Wu K, et al. Genome Sequencing of the Phytoseiid Predatory Mite Metaseiulus occidentalis Reveals Completely Atomized Hox Genes and Superdynamic Intron Evolution. Genome Biol Evol. 2016;8(6):1762-75. doi:10.1093/gbe/evw048
Kellis M, Patterson N, Endrizzi M, Birren B, Lander ES. Sequencing and comparison of yeast species to identify genes and regulatory elements. Nature. 2003;423(6937):241-54. doi:10.1038/nature01644
Grabherr MG, Russell P, Meyer M, et al. Genome-wide synteny through highly sensitive sequence alignment: Satsuma. Bioinformatics. 2010;26(9):1145-51. doi:10.1093/bioinformatics/btq102
Meissner A, Mikkelsen TS, Gu H, et al. Genome-scale DNA methylation maps of pluripotent and differentiated cells. Nature. 2008;454(7205):766-70. doi:10.1038/nature07107
Calvo S, Jain M, Xie X, et al. Systematic identification of human mitochondrial disease genes through integrative genomics. Nat Genet. 2006;38(5):576-82. doi:10.1038/ng1776
Ebert BL, Golub TR. Genomic approaches to hematologic malignancies. Blood. 2004;104(4):923-32. doi:10.1182/blood-2004-01-0274