Role of non-coding sequence variants in cancer-Reference-Cited by-同舟云学术

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Role of non-coding sequence variants in cancer

Published:2016-01-19 Issue:2 Volume:17 Page:93-108
ISSN:1471-0056
Container-title:Nature Reviews Genetics
language:en
Short-container-title:Nat Rev Genet

Author:

Khurana Ekta,Fu Yao,Chakravarty Dimple,Demichelis Francesca,Rubin Mark A.,Gerstein Mark

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

http://www.nature.com/articles/nrg.2015.17.pdf

Reference155 articles.

1. Kandoth, C. et al. Mutational landscape and significance across 12 major cancer types. Nature 502, 333–339 (2013).

2. Easton, D. F. & Eeles, R. A. Genome-wide association studies in cancer. Hum. Mol. Genet. 17, R109–R115 (2008).

3. Maurano, M. T. et al. Systematic localization of common disease-associated variation in regulatory DNA. Science 337, 1190–1195 (2012).

4. Chen, C. Y., Chang, I. S., Hsiung, C. A. & Wasserman, W. W. On the identification of potential regulatory variants within genome wide association candidate SNP sets. BMC Med. Genomics 7, 34 (2014).

5. Akhtar-Zaidi, B. et al. Epigenomic enhancer profiling defines a signature of colon cancer. Science 336, 736–739 (2012).

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