Search Results - Teague, Jon 

VAGrENT: Variation Annotation Generator by Menzies, Andy, Teague, Jon W., Butler, Adam P., Davies, Helen, Tarpey, Patrick, Nik-Zainal, Serena, Campbell, Peter J.

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cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data by Jones, David, Raine, Keiran M., Davies, Helen, Tarpey, Patrick S., Butler, Adam P., Teague, Jon W., Nik-Zainal, Serena, Campbell, Peter J.

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cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing by Raine, Keiran M., Hinton, Jonathan, Butler, Adam P., Teague, Jon W., Davies, Helen, Tarpey, Patrick, Nik-Zainal, Serena, Campbell, Peter J.

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ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data by Raine, Keiran M., Van Loo, Peter, Wedge, David C., Jones, David, Menzies, Andrew, Butler, Adam P., Teague, Jon W., Tarpey, Patrick, Nik-Zainal, Serena, Campbell, Peter J.

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Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation by Molinari, Florence, Foulquier, François, Tarpey, Patrick S., Morelle, Willy, Boissel, Sarah, Teague, Jon, Edkins, Sarah, Futreal, P. Andrew, Stratton, Michael R., Turner, Gillian, Matthijs, Gert, Gecz, Jozef, Munnich, Arnold, Colleaux, Laurence

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COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer by Forbes, Simon A., Tang, Gurpreet, Bindal, Nidhi, Bamford, Sally, Dawson, Elisabeth, Cole, Charlotte, Kok, Chai Yin, Jia, Mingming, Ewing, Rebecca, Menzies, Andrew, Teague, Jon W., Stratton, Michael R., Futreal, P. Andrew

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Mining cancer genomes in COSMIC by Jia, Mingming, Forbes, Simon A, Beare, David, Bindal, Nidhi, Gunasekaran, Prasad, Leung, Kenric, Kok, Chai Yin, Bamford, Sally, Cole, Charlotte, Ward, Sari, Teague, Jon, Stratton, Michael R, Campbell, Peter, Futreal, Andrew

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COSMIC: the catalogue of somatic mutations in cancer by Bindal, Nidhi, Forbes, Simon A, Beare, David, Gunasekaran, Prasad, Leung, Kenric, Kok, Chai Yin, Jia, Mingming, Bamford, Sally, Cole, Charlotte, Ward, Sari, Teague, Jon, Stratton, Michael R, Campbell, Peter, Futreal, Andrew P

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A survey of homozygous deletions in human cancer genomes by Cox, Charles, Bignell, Graham, Greenman, Chris, Stabenau, Arne, Warren, William, Stephens, Philip, Davies, Helen, Watt, Stephen, Teague, Jon, Edkins, Sara, Birney, Ewan, Easton, Douglas F., Wooster, Richard, Futreal, P. Andrew, Stratton, Michael R.

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COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer by Forbes, Simon A., Bindal, Nidhi, Bamford, Sally, Cole, Charlotte, Kok, Chai Yin, Beare, David, Jia, Mingming, Shepherd, Rebecca, Leung, Kenric, Menzies, Andrew, Teague, Jon W., Campbell, Peter J., Stratton, Michael R., Futreal, P. Andrew

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Data mining using the Catalogue of Somatic Mutations in Cancer BioMart by 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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COSMIC: exploring the world's knowledge of somatic mutations in human cancer by Forbes, Simon A., Beare, David, Gunasekaran, Prasad, Leung, Kenric, Bindal, Nidhi, Boutselakis, Harry, Ding, Minjie, Bamford, Sally, Cole, Charlotte, Ward, Sari, Kok, Chai Yin, Jia, Mingming, De, Tisham, Teague, Jon W., Stratton, Michael R., McDermott, Ultan, Campbell, Peter J.

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Polygenic in vivo validation of cancer mutations using transposons by Chew, Su Kit, Lu, Dong, Campos, Lia S, Scott, Kenneth L, Saci, Abdel, Wang, Juexuan, Collinson, Adam, Raine, Keiran, Hinton, Jonathan, Teague, Jon W, Jones, David, Menzies, Andrew, Butler, Adam P, Gamble, John, O’Meara, Sarah, McLaren, Stuart, Chin, Lynda, Liu, Pentao, Futreal, P Andrew

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Uptake of invitations to a lung health check offering low-dose CT lung cancer screening among an ethnically and socioeconomically diverse population at risk of lung cancer in the U... by Dickson, Jennifer L, Hall, Helen, Horst, Carolyn, Tisi, Sophie, Verghese, Priyam, Mullin, Anne-Marie, Teague, Jon, Farrelly, Laura, Bowyer, Vicky, Gyertson, Kylie, Bojang, Fanta, Levermore, Claire, Anastasiadis, Tania, McCabe, John, Navani, Neal, Nair, Arjun, Devaraj, Anand, Hackshaw, Allan, Quaife, Samantha L, Janes, Sam M

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The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene by Schwartz, Charles E, Tarpey, Patrick S, Lubs, Herbert A, Verloes, Alain, May, Melanie M, Risheg, Hiba, Friez, Michael J, Futreal, P Andrew, Edkins, Sarah, Teague, Jon, Briault, Sylvain, Skinner, Cindy, Bauer‐Carlin, Astrid, Simensen, Richard J, Joseph, Sumy M, Jones, Julie R, Gecz, Josef, Stratton, Michael R, Raymond, F Lucy, Stevenson, Roger E

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Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes by McBride, David J, Etemadmoghadam, Dariush, Cooke, Susanna L, Alsop, Kathryn, George, Joshy, Butler, Adam, Cho, Juok, Galappaththige, Danushka, Greenman, Chris, Howarth, Karen D, Lau, King W, Ng, Charlotte K, Raine, Keiran, Teague, Jon, Wedge, David C, Cancer Study Group, Australian Ovarian, Caubit, Xavier, Stratton, Michael R, Brenton, James D, Campbell, Peter J, Futreal, P Andrew, Bowtell, David DL

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SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome by Gilfillan, Gregor D., Selmer, Kaja K., Roxrud, Ingrid, Smith, Raffaella, Kyllerman, Mårten, Eiklid, Kristin, Kroken, Mette, Mattingsdal, Morten, Egeland, Thore, Stenmark, Harald, Sjøholm, Hans, Server, Andres, Samuelsson, Lena, Christianson, Arnold, Tarpey, Patrick, Whibley, Annabel, Stratton, Michael R., Futreal, P. Andrew, Teague, Jon, Edkins, Sarah, Gecz, Jozef, Turner, Gillian, Raymond, F. Lucy, Schwartz, Charles, Stevenson, Roger E., Undlien, Dag E., Strømme, Petter

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Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing by Campbell, Peter J, Stephens, Philip J, Pleasance, Erin D, O’Meara, Sarah, Li, Heng, Santarius, Thomas, Stebbings, Lucy A, Leroy, Catherine, Edkins, Sarah, Hardy, Claire, Teague, Jon W, Menzies, Andrew, Goodhead, Ian, Turner, Daniel J, Clee, Christopher M, Quail, Michael A, Cox, Antony, Brown, Clive, Durbin, Richard, Hurles, Matthew E, Edwards, Paul A W, Bignell, Graham R, Stratton, Michael R, Futreal, P Andrew

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Single-cell paired-end genome sequencing reveals structural variation per cell cycle by Voet, Thierry, Kumar, Parveen, Van Loo, Peter, Cooke, Susanna L., Marshall, John, Lin, Meng-Lay, Zamani Esteki, Masoud, Van der Aa, Niels, Mateiu, Ligia, McBride, David J., Bignell, Graham R., McLaren, Stuart, Teague, Jon, Butler, Adam, Raine, Keiran, Stebbings, Lucy A., Quail, Michael A., D’Hooghe, Thomas, Moreau, Yves, Futreal, P. Andrew, Stratton, Michael R., Vermeesch, Joris R., Campbell, Peter J.

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Analysis of the genomic landscape of multiple myeloma highlights novel prognostic markers and disease subgroups by Bolli, Niccolo, Biancon, Giulia, Moarii, Matahi, Gimondi, Silvia, Li, Yilong, de Philippis, Chiara, Maura, Francesco, Sathiaseelan, Vijitha, Tai, Yu-Tzu, Mudie, Laura, O’Meara, Sarah, Raine, Keiran, Teague, Jon W., Butler, Adam P., Carniti, Cristiana, Gerstung, Moritz, Bagratuni, Tina, Kastritis, Efstathios, Dimopoulos, Meletios, Corradini, Paolo, Anderson, Kenneth C., Moreau, Philippe, Minvielle, Stephane, Campbell, Peter J., Papaemmanuil, Elli, Avet-Loiseau, Herve, Munshi, Nikhil C.

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