Resultats de la cerca - Jon W. Teague

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  1. 1
    cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing

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

    Publicat 2015
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  2. 2
    cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data

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

    Publicat 2016
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  3. 3
    The Catalogue of Somatic Mutations in Cancer (COSMIC)

    The Catalogue of Somatic Mutations in Cancer (COSMIC) per Simon Forbes, Gurpreet Bhamra, Sally Bamford, Elisabeth Dawson, Chai Yin Kok, Jody Clements, Andrew Menzies, Jon W. Teague, P. Andrew Futreal, Michael R. Stratton

    Publicat 2008
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  4. 4
    The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

    The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website per Sally Bamford, Elisabeth Dawson, Simon Forbes, Jody Clements, Roger Pettett, Ahmet Doǧan, Adrienne M. Flanagan, Jon W. Teague, PA Futreal, Michael R. Stratton, Richard Wooster

    Publicat 2004
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  5. 5
    COSMIC 2005

    COSMIC 2005 per Simon Forbes, Jody Clements, Elisabeth Dawson, Sally Bamford, Tony Webb, Ahmet Doǧan, Adrienne M. Flanagan, Jon W. Teague, Richard Wooster, PA Futreal, Michael R. Stratton

    Publicat 2006
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  6. 6
    ascatNgs: Identifying Somatically Acquired Copy‐Number Alterations from Whole‐Genome Sequencing Data

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

    Publicat 2016
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  7. 7
    Mutations in the <i>RSK2(RPS6KA3)</i> gene cause Coffin–Lowry syndrome and nonsyndromic X‐linked mental retardation

    Mutations in the <i>RSK2(RPS6KA3)</i> gene cause Coffin–Lowry syndrome and nonsyndromic X‐linked mental retardation per Michael Field, Patrick Tarpey, J Boyle, Sarah Edkins, Judith Goodship, Ying Luo, Jennifer A. Moon, Jon W. Teague, MR Stratton, PA Futreal, Richard Wooster, FL Raymond, Gillian Turner

    Publicat 2006
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  8. 8
    COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer

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

    Publicat 2009
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  9. 9
    Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation

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

    Publicat 2008
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  10. 10
    A survey of homozygous deletions in human cancer genomes

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

    Publicat 2005
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  11. 11
    COSMIC: exploring the world's knowledge of somatic mutations in human cancer

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

    Publicat 2014
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  12. 12
    Data mining using the Catalogue of Somatic Mutations in Cancer BioMart

    Data mining using the Catalogue of Somatic Mutations in Cancer BioMart per Rebecca Shepherd, Simon Forbes, David Beare, Sally Bamford, Charlotte G. Cole, S. Ward, Nidhi Bindal, Paramasamy Gunasekaran, Mingming Jia, Chai Yin Kok, Kwong‐Sak Leung, Andrew Menzies, Adam P. Butler, Jon W. Teague, Peter J. Campbell, Michael R. Stratton, PA Futreal

    Publicat 2011
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  13. 13
    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 UK (SUMMIT): a prospective, longitudinal cohort study

    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... per Jennifer Dickson, Helen Hall, Carolyn Horst, Sophie Tisi, Priyam Verghese, Anne-Marie Mullin, Jon W. Teague, Laura Farrelly, Vicky Bowyer, Kylie Gyertson, Fanta Bojang, Claire Levermore, Tania Anastasiadis, John McCabe, Neal Navani, Arjun Nair, Anand Devaraj, Allan Hackshaw, Samantha L. Quaife, Sam M. Janes

    Publicat 2023
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  14. 14
    Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

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

    Publicat 2008
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  15. 15
    Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes

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

    Publicat 2012
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  16. 16
    Genomic Classification and Prognosis in Acute Myeloid Leukemia

    Genomic Classification and Prognosis in Acute Myeloid Leukemia per Elli Papaemmanuil, Moritz Gerstung, Lars Bullinger, Verena I. Gaidzik, Peter Paschka, Nicola D. Roberts, Nicola Potter, Michael Heuser, Felicitas Thol, Niccolò Bolli, Gunes Gundem, Peter Van Loo, Iñigo Martincorena, Peter Ganly, Laura Mudie, Stuart McLaren, Sarah O’Meara, Keiran Raine, David Jones, Jon W. Teague, Adam P. Butler, Mel Greaves, Arnold Ganser, Konstanze Döhner, Richard F. Schlenk, Hartmut Döhner, Peter J. Campbell

    Publicat 2016
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  17. 17
    SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome

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

    Publicat 2008
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  18. 18
    The patterns and dynamics of genomic instability in metastatic pancreatic cancer

    The patterns and dynamics of genomic instability in metastatic pancreatic cancer per Peter J. Campbell, Shinichi Yachida, Laura Mudie, Philip J. Stephens, Erin Pleasance, Lucy Stebbings, Laura Morsberger, Calli Latimer, Stuart McLaren, Meng-Lay Lin, David J. McBride, Ignacio Varela, Serena Nik‐Zainal, Catherine Leroy, Mingming Jia, Andrew Menzies, Adam P. Butler, Jon W. Teague, Constance A. Griffin, John H. Burton, Harold Swerdlow, Michael A. Quail, Michael R. Stratton, Christine A. Iacobuzio‐Donahue, P. Andrew Futreal

    Publicat 2010
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  19. 19
    Single-cell paired-end genome sequencing reveals structural variation per cell cycle

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

    Publicat 2013
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  20. 20
    Analysis of the genomic landscape of multiple myeloma highlights novel prognostic markers and disease subgroups

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

    Publicat 2018
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