The Role of New Sequencing Technology in Identifying Rare Mutations in New Susceptibility Genes for Cancer
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40142-013-0021-7.pdf
Reference69 articles.
1. Asan, Xu Y, Jiang H, Tyler-Smith C, et al. Comprehensive comparison of three commercial human whole-exome capture platforms. Genome Biol. 2011;12(9):R95.
2. Clark MJ, Chen R, Lam HY, et al. Performance comparison of exome DNA sequencing technologies. Nat Biotechnol. 2011;29(10):908–14.
3. Snape K, Ruark E, Tarpey P, et al. Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer. Breast Cancer Res Treat. 2012;134(1):429–33.
4. • Park DJ, Lesueur F, Nguyen-Dumont T, et al. Rare mutations in XRCC2 increase the risk of breast cancer. Am J Hum Genet. 2012;90(4):734–9. An early example of the application of MPS in the setting of multiple-case breast cancer families designed to identify new breast cancer susceptibility genes.
5. • Thompson ER, Doyle MA, Ryland GL, et al. Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles. PLoS Genet. 2012;8(9):e1002894. An early example of the application of MPS in the setting of multiple-case breast cancer families designed to identify new breast cancer susceptibility genes.
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1. Annokey: an annotation tool based on key term search of the NCBI Entrez Gene database;Source Code for Biology and Medicine;2014-06-26
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