ENCODE Project Consortium, Snyder MP, Gingeras TR, et al. Perspectives on ENCODE. Nature. 2020;583(7818):693-698. doi:10.1038/s41586-020-2449-8
ENCODE Project Consortium, Moore JE, Purcaro MJ, et al. Expanded encyclopaedias of DNA elements in the human and mouse genomes. Nature. 2020;583(7818):699-710. doi:10.1038/s41586-020-2493-4
Nash A, Sewell T, Farrer RA, et al. MARDy: Mycology Antifungal Resistance Database. Bioinformatics. 2018;34(18):3233-3234. doi:10.1093/bioinformatics/bty321
Grant AR, Hemphill SE, Vincent LM, Rehm HL. Reclassification of the p.Ile208Val variant by case-level data sharing. Cold Spring Harb Mol Case Stud. 2018;4(5). doi:10.1101/mcs.a002675
Anyansi C, Keo A, Walker BJ, et al. QuantTB - a method to classify mixed Mycobacterium tuberculosis infections within whole genome sequencing data. BMC Genomics. 2020;21(1):80. doi:10.1186/s12864-020-6486-3
Galagan JE, Sisk P, Stolte C, et al. TB database 2010: overview and update. Tuberculosis (Edinb). 2010;90(4):225-35. doi:10.1016/j.tube.2010.03.010
Musunuru K, Lettre G, Young T, et al. Candidate gene association resource (CARe): design, methods, and proof of concept. Circ Cardiovasc Genet. 2010;3(3):267-75. doi:10.1161/CIRCGENETICS.109.882696
International Cancer Genome Consortium, Hudson TJ, Anderson W, et al. International network of cancer genome projects. Nature. 2010;464(7291):993-8. doi:10.1038/nature08987
Raychaudhuri S, Plenge RM, Rossin EJ, et al. Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. PLoS Genet. 2009;5(6):e1000534. doi:10.1371/journal.pgen.1000534
Chiang DY, Getz G, Jaffe DB, et al. High-resolution mapping of copy-number alterations with massively parallel sequencing. Nat Methods. 2009;6(1):99-103. doi:10.1038/nmeth.1276