Washietl S, Will S, Hendrix DA, et al. Computational analysis of noncoding RNAs. Wiley Interdiscip Rev RNA. 2012;3(6):759-78. doi:10.1002/wrna.1134
Meschia JF, Arnett DK, Ay H, et al. Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. Stroke. 2013;44(10):2694-702. doi:10.1161/STROKEAHA.113.001857
Helman E, Lawrence MS, Stewart C, Sougnez C, Getz G, Meyerson M. Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing. Genome Res. 2014;24(7):1053-63. doi:10.1101/gr.163659.113
Yozwiak NL, Schaffner SF, Sabeti PC. Data sharing: Make outbreak research open access. Nature. 2015;518(7540):477-9. doi:10.1038/518477a
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
Dyke SOM, Philippakis AA, De Argila JR, et al. Consent Codes: Upholding Standard Data Use Conditions. PLoS Genet. 2016;12(1):e1005772. doi:10.1371/journal.pgen.1005772
Zheng J, Erzurumluoglu M, Elsworth BL, et al. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. Bioinformatics. 2017;33(2):272-279. doi:10.1093/bioinformatics/btw613
Brudno Y, Birnbaum ME, Kleiner RE, Liu DR. An in vitro translation, selection and amplification system for peptide nucleic acids. Nat Chem Biol. 2010;6(2):148-55. doi:10.1038/nchembio.280