References
- Liu L, Li Y, Li S, et al. Comparison of Next-Generation Sequencing Systems. J. Biomed. Biotechnol. 2012, 11 (2012).
- Jiang Q, Turner T, Sosa MX, Rakha A, Arnold S, Chakravarti A. Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer. Hum Mutat. 33(1), 281–289 (2012).
- Chan M, Ji SM, Yeo ZX, et al. Development of a next-generation sequencing method for BRCA mutation screening: a comparison between a high-throughput and a benchtop platform. J. Mol. Diagn. 14(6), 602–612 (2012).
- Costa JL, Sousa S, Justino A, et al. Nonoptical massive parallel DNA sequencing of BRCA1 and BRCA2 genes in a diagnostic setting. Hum Mutat. 34(4), 629–635 (2013).
- Loman NJ, Misra RV, Dallman TJ, et al. Performance comparison of benchtop high-throughput sequencing platforms. Nat Biotechnol. 30(5),434–439 (2012).
- DePristo MA, Banks E, Poplin R et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43(5), 491–498 (2011).
- Yeo ZX, Chan M, Yap YS, Ang P, Rozen S, Lee AS. Improving indel detection specificity of the Ion Torrent PGM benchtop sequencer. PLoS One 7(9), e45798 (2012).
- Morgan JE, Carr IM, Sheridan E et al. Genetic diagnosis of familial breast cancer using clonal sequencing. Hum. Mutat. 31(4), 484–491 (2010).
- Jiang Q, Turner T, Sosa M, Rakha A, Arnold S, Chakravarti A. Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer. Hum. Mutat. 33(1), 281–289 (2011).
- Meldrum C, Doyle MA, Tothill RW. Next-generation sequencing for cancer diagnostics: a practical perspective. Clin. Biochem Rev. 32(4), 177–195 (2011).
- Shyr D, Liu Q. Next generation sequencing in cancer research and clinical application. Biol Proced. Online 15(1), 4 (2013).
- Gullapalli RR, Desai KV, Santana-Santos L, Kant JA, Becich MJ. Next generation sequencing in clinical medicine: Challenges and lessons for pathology and biomedical informatics. J. Pathol. Inform. 3, 40 (2012).
Website
- Foundation One.www.foundationone.com
- MedlinePlus. 10 years on, still much to be learned from Human Genome Map US: NIH; 2013. www.nlm.nih.gov/medlineplus/news/fullstory_135866.html ( Accessed 5 May 2013)
- GenomeWeb. Myriad to replace BRACAnalysis, other hereditary cancer tests with MyRisk Panel 2013. www.genomeweb.com//node/1228081?hq_e=el&hq_m=1580639&hq_l=1&hq_v=d01443c25c ( Accessed 10 May 2013)