Biagioli M, Ferrari F, Mendenhall EM, et al. Htt CAG repeat expansion confers pleiotropic gains of mutant huntingtin function in chromatin regulation. Hum Mol Genet. 2015;24(9):2442-57. doi:10.1093/hmg/ddv006
Stitziel NO, Peloso GM, Abifadel M, et al. Exome sequencing in suspected monogenic dyslipidemias. Circ Cardiovasc Genet. 2015;8(2):343-50. doi:10.1161/CIRCGENETICS.114.000776
Kim H, Zheng S, Amini SS, et al. Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution. Genome Res. 2015;25(3):316-27. doi:10.1101/gr.180612.114
Lubitz SA, Ellinor PT. Somatic mutations and atrial fibrillation: the end or just the beginning? Circ Cardiovasc Genet. 2015;8(1):2-3. doi:10.1161/CIRCGENETICS.115.000963
Stremlau MH, Andersen KG, Folarin OA, et al. Discovery of novel rhabdoviruses in the blood of healthy individuals from West Africa. PLoS Negl Trop Dis. 2015;9(3):e0003631. doi:10.1371/journal.pntd.0003631
Shalem O, Sanjana NE, Zhang F. High-throughput functional genomics using CRISPR-Cas9. Nat Rev Genet. 2015;16(5):299-311. doi:10.1038/nrg3899
Satija R, Farrell JA, Gennert D, Schier AF, Regev A. Spatial reconstruction of single-cell gene expression data. Nat Biotechnol. 2015;33(5):495-502. doi:10.1038/nbt.3192
Bambury RM, Bhatt AS, Riester M, et al. DNA copy number analysis of metastatic urothelial carcinoma with comparison to primary tumors. BMC Cancer. 2015;15:242. doi:10.1186/s12885-015-1192-2
Franzosa EA, Hsu T, Sirota-Madi A, et al. Sequencing and beyond: integrating molecular ’omics’ for microbial community profiling. Nat Rev Microbiol. 2015;13(6):360-72. doi:10.1038/nrmicro3451
Li H. BFC: correcting Illumina sequencing errors. Bioinformatics. 2015;31(17):2885-7. doi:10.1093/bioinformatics/btv290