Author:
Singh R R,Patel K P,Routbort M J,Aldape K,Lu X,Manekia J,Abraham R,Reddy N G,Barkoh B A,Veliyathu J,Medeiros L J,Luthra R
Publisher
Springer Science and Business Media LLC
Reference22 articles.
1. Beadling C, Neff TL, Heinrich MC, Rhodes K, Thornton M, Leamon J, Andersen M, Corless CL (2013) Combining highly multiplexed PCR with semiconductor-based sequencing for rapid cancer genotyping. J Mo Diagn 15 (2): 171–176.
2. Bielinski SJ, Olson JE, Pathak J, Weinshilboum RM, Wang L, Lyke KJ, Ryu E, Targonski PV, Van Norstrand MD, Hathcock MA, Takahashi PY, McCormick JB, Johnson KJ, Maschke KJ, Rohrer Vitek CR, Ellingson MS, Wieben ED, Farrugia G, Morrisette JA, Kruckeberg KJ, Bruflat JK, Peterson LM, Blommel JH, Skierka JM, Ferber MJ, Black JL, Baudhuin LM, Klee EW, Ross JL, Veldhuizen TL, Schultz CG, Caraballo PJ, Freimuth RR, Chute CG, Kullo IJ (2014) Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol. Mayo Clin Proc 89 (1): 25–33.
3. Bowcock AM (2013) Invited review DNA copy number changes as diagnostic tools for lung cancer. Thorax 69 (5): 495–496.
4. Dutton-Regester K, Hayward NK (2012) Whole genome and exome sequencing of melanoma: a step toward personalized targeted therapy. Adv Pharmacol 65: 399–435.
5. Forbes SA, Bhamra G, Bamford S, Dawson E, Kok C, Clements J, Menzies A, Teague JW, Futreal PA, Stratton MR (2008) The Catalogue of Somatic Mutations in Cancer (COSMIC). Curr Protoc Hum Gen 57: 10.11.1–10.11.26.
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