Category: 2012

Whole-exome sequencing combined with functional genomics reveals novel candidate driver cancer genes in endometrial cancer W

Liang H, Cheung LWT, Li J, Ju Z, Yu S, Stemke-Hale K, Dogruluk T, Lu Y, Liu X, Gu C, Scherer SE, Carter H, Westin SN, Verhaak R, Zhang F, Karchin R, Liu CG, Lu KH, Broaddus RR, Scott KL, Hennessy BT, Mills GB (2012) Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer …

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Charting the landscape of tandem BRCT domain-mediated protein interactions C

Woods N, Mesquita RD, Sweet M, Carvalho MA, Li X, Liu Y, Nguyen H, Marsillac S, Karchin R, Koomen J, Monteiro ANA(2012) Charting the landscape of tandem BRCT domain-mediated protein interactions. Science Signaling. 5(242):rs6

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Phenotype-optimized sequence ensembles substantially improve prediction of disease-causing mutation in cystic fibrosis P

Masica DL, Sosnay P, Cutting G, Karchin R (2012) Phenotype-optimized sequence ensembles substantially improve prediction of disease-causing mutation in cystic fibrosis. Human Mutation. 33(8):1267-74

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Somatic mutations in the Notch, NF-KB, PIK3CA, and Hedgehog pathways in human breast cancers S

Jiao X, Wood L, Lindman M, Jones S, Buckhaults P, Polyak K, Sukumar S, Carter H, Kim D, Karchin R and Sjobolom T (2012) Somatic mutations in the notch, NF-KB, PIK3CA and hedgehog pathways in human breast cancers. Genes, Chromosomes and Cancer. 51(5):480-9

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