FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer
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Springer Science and Business Media LLC
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http://link.springer.com/content/pdf/10.1186/s13059-014-0480-5.pdf
Reference57 articles.
1. Greenman C, Stephens P, Smith R, Dalgliesh GL, Hunter C, Bignell G, Davies H, Teague J, Butler A, Stevens C, Edkins S, O'Meara S, Vastrik I, Schmidt EE, Avis T, Barthorpe S, Bhamra G, Buck G, Choudhury B, Clements J, Cole J, Dicks E, Forbes S, Gray K, Halliday K, Harrison R, Hills K, Hinton J, Jenkinson A, Jones D, et al: Patterns of somatic mutation in human cancer genomes. Nature. 2007, 446: 153-158. 10.1038/nature05610.
2. Futreal PA, Coin L, Marshall M, Down T, Hubbard T, Wooster R, Rahman N, Stratton MR: A census of human cancer genes. Nat Rev Cancer. 2004, 4: 177-183. 10.1038/nrc1299.
3. Dees ND, Zhang Q, Kandoth C, Wendl MC, Schierding W, Koboldt DC, Mooney TB, Callaway MB, Dooling D, Mardis ER, Wilson RK, Ding L: MuSiC: identifying mutational significance in cancer genomes. Genome Res. 2012, 22: 1589-1598. 10.1101/gr.134635.111.
4. Reimand J, Bader GD: Systematic analysis of somatic mutations in phosphorylation signaling predicts novel cancer drivers. Mol Syst Biol. 2013, 9: 637-10.1038/msb.2012.68.
5. Tamborero D, Gonzalez-Perez A, Lopez-Bigas N: OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes. Bioinformatics. 2013, 29: 2238-2244. 10.1093/bioinformatics/btt395.
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