COSMIC: somatic cancer genetics at high-resolution von Forbes, Simon A, Beare, David, Boutselakis, Harry, Bamford, Sally, Bindal, Nidhi, Tate, John, Cole, Charlotte G, Ward, Sari, Dawson, Elisabeth, Ponting, Laura, Stefancsik, Raymund, Harsha, Bhavana, Kok, Chai Yin, Jia, Mingming, Jubb, Harry, Sondka, Zbyslaw, Thompson, Sam, De, Tisham, Campbell, Peter J

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The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers von Sondka, Zbyslaw, Bamford, Sally, Cole, Charlotte G., Ward, Sari A., Dunham, Ian, Forbes, Simon A.

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COSMIC: the Catalogue Of Somatic Mutations In Cancer von Tate, John G, Bamford, Sally, Jubb, Harry C, Sondka, Zbyslaw, Beare, David M, Bindal, Nidhi, Boutselakis, Harry, Cole, Charlotte G, Creatore, Celestino, Dawson, Elisabeth, Fish, Peter, Harsha, Bhavana, Hathaway, Charlie, Jupe, Steve C, Kok, Chai Yin, Noble, Kate, Ponting, Laura, Ramshaw, Christopher C, Rye, Claire E, Speedy, Helen E, Stefancsik, Ray, Thompson, Sam L, Wang, Shicai, Ward, Sari, Campbell, Peter J, Forbes, Simon A

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms von Sachidanandam, R, Weissman, D, Schmidt, S C, Kakol, J M, Stein, L D, Marth, G, Sherry, S, Mullikin, J C, Mortimore, B J, Willey, D L, Hunt, S E, Cole, C G, Coggill, P C, Rice, C M, Ning, Z, Rogers, J, Bentley, D R, Kwok, P Y, Mardis, E R, Yeh, R T, Schultz, B, Cook, L, Davenport, R, Dante, M, Fulton, L, Hillier, L, Waterston, R H, McPherson, J D, Gilman, B, Schaffner, S, Van Etten, W J, Reich, D, Higgins, J, Daly, M J, Blumenstiel, B, Baldwin, J, Stange-Thomann, N, Zody, M C, Linton, L, Lander, E S, Altshuler, D

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Data mining using the Catalogue of Somatic Mutations in Cancer BioMart von Shepherd, Rebecca, Forbes, Simon A, Beare, David, Bamford, S, Cole, Charlotte G, Ward, Sari, Bindal, Nidhi, Gunasekaran, Prasad, Jia, Mingming, Kok, Chai Yin, Leung, Kenric, Menzies, Andrew, Butler, Adam P, Teague, Jon W, Campbell, Peter J, Stratton, Michael R, Futreal, P Andrew

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Finishing the finished human chromosome 22 sequence von Cole, Charlotte G, McCann, Owen T, Collins, John E, Oliver, Karen, Willey, David, Gribble, Susan M, Yang, Fengtang, McLaren, Karen, Rogers, Jane, Ning, Zemin, Beare, David M, Dunham, Ian

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Reevaluating human gene annotation: a second-generation analysis of chromosome 22 von Collins, John E, Goward, Melanie E, Cole, Charlotte G, Smink, Luc J, Huckle, Elizabeth J, Knowles, Sarah, Bye, Jacqueline M, Beare, David M, Dunham, Ian

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Abstract 2469: The COSMIC Cancer Gene Census - a comprehensive study of all mutated cancer-driving genes von Sondka, Zbyslaw, Speedy, Helen E., Bamford, Sally, Cole, Charlotte G., Ward, Sari A., Forbes, Simon A.

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Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify t... von LANGAN, Joanne E, COLE, Charlotte G, DUNHAM, Ian, FIELD, John K, RISK, Janet M, HUCKLE, Elisabeth J, BYRNE, Shaun, MCRONALD, Fiona E, ROWBOTTOM, Lynn, ELLIS, Anthony, SHAW, Joan M, LEIGH, Irene M, KELSELL, David P

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Abstract 2599: COSMIC Cancer Gene Census: expert descriptions across genes in oncogenesis von Sondka, Zbyslaw, Bamford, Sally, Cole, Charlotte G., Dawson, Elisabeth, Ponting, Laura, Stefancsik, Raymund, Ward, Sari A., Tate, John, Campbell, Peter J., Forbes, Simon A.

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Abstract 3284: COSMIC: Integrating and interpreting the world's knowledge of somatic mutations in cancer von Sondka, Zbyslaw, Bamford, Sally, Cole, Charlotte G., Dawson, Elisabeth, Ponting, Laura, Stefancsik, Raymund, Ward, Sari, Jubb, Harry C., Thompson, Sam, Beare, Dave, Bindal, Nidhi, Boutselakis, Charambulos, Fish, Peter, Harsha, Bhavana, Kok, Chai Yin, Ramshaw, Chris, Rye, Claire, Tate, John, Wang, Shicai, Campbell, Peter J., Forbes, Simon A.

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Abstract 5285: COSMIC: comprehensively exploring oncogenomics von Forbes, Simon A., Bindal, Nidhi, Beare, David, Bamford, Sally, Cole, Charlotte G., Ward, Sari, Leung, Kenric, Kok, Chai Yin, Jia, Mingming, De, Tisham, Sondka, Zbyslaw, Stratton, Michael R., Campbell, Peter J.

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A genome annotation-driven approach to cloning the human ORFeome von Collins, John E, Wright, Charmain L, Edwards, Carol A, Davis, Matthew P, Grinham, James A, Cole, Charlotte G, Goward, Melanie E, Aguado, Begoña, Mallya, Meera, Mokrab, Younes, Huckle, Elizabeth J, Beare, David M, Dunham, Ian

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Fine-Mapping, Genomic Organization, and Transcript Analysis of the Human Ubiquitin-Conjugating Enzyme Gene UBE2L3 von Moynihan, Terry P., Cole, Charlotte G., Dunham, Ian, O'Neil, Lisa, Markham, Alexander F., Robinson, Philip A.

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PRENATAL TESTING FOR DUCHENNE AND BECKER MUSCULAR DYSTROPHY von Cole, CharlotteG, Coyne, Anita, Hart, KevinA, Sheridan, Richard, Walker, Alison, Johnson, Lynn, Hodgson, Shirley, Bobrow, Martin

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A high-density YAC contig map of human chromosome 22 von Collins, J E, Cole, C G, Smink, L J, Garrett, C L, Leversha, M A, Soderlund, C A, Maslen, G L, Everett, L A, Rice, K M, Coffey, A J

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Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer von Langan, Joanne E, Cole, Charlotte G, Huckle, Elisabeth J, Byrne, Shaun, McRonald, Fiona E, Rowbottom, Lynn, Ellis, Anthony

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Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach von Coffey, Alison J., Roberts, Roland G., Green, Eric D., Cole, Charlotte G., Butler, Rachel, Anand, Rakesh, Giannelli, Francesco, Bentley, David R.

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The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers von Sondka, Zbyslaw, Bamford, Sally, Cole, Charlotte G, Ward, Sari A, Dunham, Ian, Forbes, Simon A

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Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3 von FORBES, S. A, BRENNAN, L, RICHARDSON, M, COFFEY, A, COLE, C. G, GREGORY, S. G, BENTLEY, D. R, MUMM, S, MOORE, G. E, STANIER, P

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