Arora K, Shah M, Johnson M, Sanghvi R, Shelton J, Nagulapalli K, Oschwald DM, Zody MC, Germer S, Jobanputra V, Carter J, Robine N (2019) Deep sequencing of 3 cancer cell lines on 2 sequencing platforms. bioRxiv. https://doi.org/10.1101/623702
Attaran M (2017) The rise of 3-D printing: the advantages of additive manufacturing over traditional manufacturing. Bus Horiz 60:677-688 doi: 10.1016/j.bushor.2017.05.011
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ (2011) A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 43:491-498 doi: 10.1038/ng.806
Gross BC, Erkal JL, Lockwood SY, Chen CP, Spence DM (2014) Evaluation of 3D printing and its potential impact on biotechnology and the chemical sciences. Anal Chem 86:3240-3253 doi: 10.1021/ac403397r
Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25:1754-1760 doi: 10.1093/bioinformatics/btp324
Long H, Miller SF, Strauss C, Zhao C, Cheng L, Ye Z, Griffin K, Te R, Lee H, Chen CC, Lynch M (2016) Antibiotic treatment enhances the genome-wide mutation rate of target cells. Proc Natl Acad Sci USA 113:E2498-E2505 doi: 10.1073/pnas.1601208113
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, DePristo MA (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20:1297-1303 doi: 10.1101/gr.107524.110
Mora-Castilla S, To C, Vaezeslami S, Morey R, Srinivasan S, Dumdie JN, Cook-Andersen H, Jenkins J, Laurent LC (2016) Miniaturization technologies for efficient single-cell library preparation for next-generation sequencing. J Lab Autom 21:557-567 doi: 10.1177/2211068216630741
Morozova O, Hirst M, Marra MA (2009) Applications of new sequencing technologies for transcriptome analysis. Annu Rev Genomics Hum Genet 10:135-151 doi: 10.1146/annurev-genom-082908-145957
Navin N, Kendall J, Troge J, Andrews P, Rodgers L, McIndoo J, Cook K, Stepansky A, Levy D, Esposito D, Muthuswamy L, Krasnitz A, McCombie WR, Hicks J, Wigler M (2011) Tumour evolution inferred by single-cell sequencing. Nature 472:90-94 doi: 10.1038/nature09807
Ogiso-Tanaka E, Kaga A, Hajika M (2018) Miniaturization technologies for cost-effective AmpliSeq library preparation for next generation sequencing. J Appl Microb Res 1:43-49 
Van der Auwera GA, Carneiro MO, Hartl C, Poplin R, Del Angel G, Levy-Moonshine A, Jordan T, Shakir K, Roazen D, Thibault J, Banks E, Garimella KV, Altshuler D, Gabriel S, DePristo MA (2013) From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline. Curr Protoc Bioinform 43: 11.10.1-11.10.33
van Dijk EL, Auger H, Jaszczyszyn Y, Thermes C (2014) Ten years of next-generation sequencing technology. Trends Genet 30:418-426 doi: 10.1016/j.tig.2014.07.001