Author:
Craig David W.,Nasser Sara,Corbett Richard,Chan Simon K.,Murray Lisa,Legendre Christophe,Tembe Waibhav,Adkins Jonathan,Kim Nancy,Wong Shukmei,Baker Angela,Enriquez Daniel,Pond Stephanie,Pleasance Erin,Mungall Andrew J.,Moore Richard A.,McDaniel Timothy,Ma Yussanne,Jones Steven J. M.,Marra Marco A.,Carpten John D.,Liang Winnie S.
Publisher
Springer Science and Business Media LLC
Reference44 articles.
1. Zook, J. M. et al. Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls. Nat Biotechnol. 32, 246–251 (2014).
2. Eberle, M. A. et al. Platinum Genomes: A systematic assessment of variant accuracy using a large family pedigree. Presented at the 60th Annual Meeting of The American Society of Human Genetics, October 22–26, Boston (2013)
3. Lin, M. T. et al. Clinical validation of KRAS, BRAF, and EGFR mutation detection using next-generation sequencing. Am J Clin Pathol. 141, 856–866 (2014).
4. Linderman, M. D. et al. Analytical validation of whole exome and whole genome sequencing for clinical applications. BMC Med Genomics. 7, 20; doi: 10.1186/1755-8794-7-20 (2014).
5. Simen, B. B. et al. Validation of a Next-Generation-Sequencing Cancer Panel for Use in the Clinical Laboratory. Arch Pathol Lab Med. 139, 508–517 (2015).
Cited by
63 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献