Hakutulokset - Jennifer Becq
- Näytetään 1 - 16 yhteensä 16 tuloksesta
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A Benchmark of Parametric Methods for Horizontal Transfers Detection Tekijä Jennifer Becq, Cécile Churlaud, Patrick Deschavanne
Julkaistu 2010Artigo -
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Genomic Variation among Contemporary Pseudomonas aeruginosa Isolates from Chronically Infected Cystic Fibrosis Patients Tekijä Jade C. S. Chung, Jennifer Becq, Louise Fraser, Ole Schulz-Trieglaff, Nicholas J. Bond, J. Foweraker, Kenneth D. Bruce, Geoffrey Smith, Martin Welch
Julkaistu 2012Artigo -
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Whole-Genome Sequencing for Rapid Susceptibility Testing of <i>M. tuberculosis</i> Tekijä Claudio U. Köser, Josephine M. Bryant, Jennifer Becq, M. Estée Török, Matthew J. Ellington, Marc A. Martı́-Renom, Andrew Carmichael, Julian Parkhill, Geoffrey Smith, Sharon J. Peacock
Julkaistu 2013Carta -
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Rapid single-colony whole-genome sequencing of bacterial pathogens Tekijä Claudio U. Köser, Louise Fraser, Alexandros Ioannou, Jennifer Becq, M.J. Ellington, Matthew T. G. Holden, Sandra Reuter, M. Estée Török, Stephen D. Bentley, Julian Parkhill, N. A. Gormley, Geoffrey Smith, Sharon J. Peacock
Julkaistu 2013Artigo -
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Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns Tekijä Anna Schuh, Jennifer Becq, Sean Humphray, Adrian Alexa, Adam Burns, Ruth Clifford, Stephan M. Feller, Russell Grocock, Shirley Henderson, Irina Khrebtukova, Zoya Kingsbury, Shujun Luo, David J. McBride, Lisa Murray, Toshi Menju, Adele Timbs, Mark T. Ross, Jenny C. Taylor, David Bentley
Julkaistu 2012Artigo -
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Analysis of Circulating Tumor DNA to Monitor Metastatic Breast Cancer Tekijä Sarah‐Jane Dawson, Dana W.Y. Tsui, Muhammed Murtaza, Heather Biggs, Oscar M. Rueda, Suet‐Feung Chin, Mark Dunning, Davina Gale, Tim Forshew, Betania Mahler‐Araujo, Sabrina Rajan, Sean Humphray, Jennifer Becq, David Halsall, Matthew Wallis, David Bentley, Carlos Caldas, Nitzan Rosenfeld
Julkaistu 2013Artigo -
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Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups Tekijä Adam Burns, Reem Alsolami, Jennifer Becq, Basile Stamatopoulos, Adele Timbs, Dara Bruce, Pauline Robbe, Dimitris Vavoulis, Ruth Clifford, Maité Cabes, Hélène Dreau, Jenny C. Taylor, Samantha J.L. Knight, Robert Månsson, D. R. Bentley, Renée Beekman, José I. Martı́n-Subero, Elı́as Campo, Richard S. Houlston, Kate Ridout, Anna Schuh
Julkaistu 2017Artigo -
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Glioblastoma adaptation traced through decline of an IDH1 clonal driver and macro-evolution of a double-minute chromosome Tekijä Francesco Favero, Nicholas McGranahan, Maximilian P Salm, Nicolai J. Birkbak, Zack Sanborn, Stephen C. Benz, Jennifer Becq, John F. Peden, Zoya Kingsbury, R.J. Grocok, Sean Humphray, D. R. Bentley, Bradley Spencer‐Dene, Alice Gutteridge, M. Brada, Sébastien Roger, Pierre‐Yves Dietrich, Tim Forshew, Marco Gerlinger, Andrew Rowan, Gordon Stamp, Aron C. Eklund, Zoltán Szállási, Charles Swanton
Julkaistu 2015Artigo -
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Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project Tekijä Pauline Robbe, Niko Popitsch, Samantha J.L. Knight, Pavlos Antoniou, Jennifer Becq, Miao He, Alexander Kanapin, Anastasia Samsonova, Dimitrios V. Vavoulis, Mark T. Ross, Zoya Kingsbury, Maité Cabes, Sara D.C. Ramos, Suzanne Page, Hélène Dreau, Kate Ridout, J. Louise Jones, Alice Tuff-Lacey, Shirley Henderson, Joanne Mason, Francesca M. Buffa, Clare Verrill, David Maldonado‐Pérez, Ioannis Roxanis, Elena Collantes, Lisa Browning, Sunanda Dhar, Stephen Damato, S. J. Davies, Mark J. Caulfield, David Bentley, Jenny C. Taylor, Clare Turnbull, Anna Schuh
Julkaistu 2018Artigo -
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Epigenetic regulator genes direct lineage switching in <i>MLL/AF4</i> leukemia Tekijä Ricky Tirtakusuma, Katarzyna Szołtysek, Paul Milne, Vasily V. Grinev, Anetta Ptasinska, Paulynn Suyin Chin, Claus Meyer, Sirintra Nakjang, Jayne Y. Hehir‐Kwa, Daniel Williamson, Pierre Cauchy, Peter Keane, Salam A. Assi, Minoo Ashtiani, Sophie G. Kellaway, Maria Rosaria Imperato, Fotini Vogiatzi, Elizabeth K. Schweighart, Shan Lin, Mark Wunderlich, Janine Stutterheim, Alexander Komkov, Elena Zerkalenkova, Paul Evans, Hesta McNeill, Alex Elder, Natalia Martinez-Soria, Sarah Fordham, Yuzhe Shi, Lisa J. Russell, Deepali Pal, Alexandra Smith, Zoya Kingsbury, Jennifer Becq, Cornelia Eckert, Oskar A. Haas, Peter Carey, Simon Bailey, Roderick Skinner, Natalia Miakova, Matthew Collin, Venetia Bigley, Muzlifah Haniffa, Rolf Marschalek, Christine J. Harrison, Catherine Cargo, Denis M. Schewe, Yulia Olshanskaya, Michael J. Thirman, Peter N. Cockerill, James C. Mulloy, Helen J. Blair, Josef Vormoor, James M. Allan, Constanze Bonifer, Olaf Heidenreich, Simon Bomken
Julkaistu 2022Artigo -
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Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer Tekijä Elizabeth P. Murchison, Ole Schulz-Trieglaff, Zemin Ning, Ludmil B. Alexandrov, Markus Bauer, Beiyuan Fu, Matthew M. Hims, Zhihao Ding, Sergii Ivakhno, Caitlin M. Stewart, Bee Ling Ng, Wendy S.W. Wong, Bronwen Aken, Simon White, Amber E. Alsop, Jennifer Becq, Graham R. Bignell, R. Keira Cheetham, William Cheng, Thomas R. Connor, Anthony J. Cox, Zhiping Feng, Yong Gu, Russell Grocock, Simon R. Harris, Irina Khrebtukova, Zoya Kingsbury, Mark Kowarsky, Alexandre Kreiss, Shujun Luo, John Marshall, David J. McBride, Lisa Murray, Anne‐Maree Pearse, Keiran Raine, Isabelle Rasolonjatovo, Richard J. Shaw, Philip Tedder, Carolyn Tregidgo, Albert J. Vilella, David C. Wedge, GM Woods, Niall Gormley, Sean Humphray, Gary P. Schroth, Geoffrey Smith, Kevin P. Hall, Stephen M. J. Searle, Nigel P. Carter, Anthony T. Papenfuss, P. Andrew Futreal, Peter J. Campbell, Fengtang Yang, David Bentley, Dirk J. Evers, Michael R. Stratton
Julkaistu 2012Artigo -
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Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma Tekijä Caryn S. Ross-Innes, Jennifer Becq, Andrew Warren, R. Keira Cheetham, Helen Northen, Maria O’Donovan, Shalini Malhotra, Massimiliano di Pietro, Sergii Ivakhno, Miao He, Jamie Weaver, Andy G. Lynch, Zoya Kingsbury, Mark T. Ross, Sean Humphray, David Bentley, Rebecca C. Fitzgerald, Stephen J. Hayes, Yeng Ang, Ian Welch, Shaun R. Preston, Sarah Oakes, Vicki Save, Richard J. E. Skipworth, Olga Tucker, Jim Davies, Charles Crichton, Christian Schusterreiter, Tim Underwood, Fergus Noble, Bernard Stacey, Jamie Kelly, James D. Byrne, Annette Haydon, Donna Sharland, Jack Owsley, Hugh Barr, Jesper Lagergren, James Gossage, Andrew Davies, Robert C. Mason, Fuju Chang, Janine Zylstra, Grant Sanders, Tim Wheatley, Richard Berrisford, Tim Bracey, Catherine Harden, David Bunting, Tom Roques, Jenny Nobes, Suat Loo, Mike Lewis, Ed Cheong, Oliver Priest, Simon L. Parsons, Irshad Soomro, Philip Kaye, J. Saunders, Junxiong Pang, Neil T. Welch, James Catton, John P. Duffy, Krish Ragunath, Laurence Lovat, Rehan Haidry, Haroon Miah, Sarah Kerr, Victor Eneh, Rommel Butawan, Tom Roques, Michael Lewis, Edward Cheong, Bhaskar Kumar, Laszlo Igali, Sharon Walton, Adela Dann, Peter Safranek, Andrew Hindmarsh, Vijayendran Sudjendran, Michael Scott, Alison D. Cluroe, Ahmad Miremadi, Betania Mahler‐Araujo, Barbara Nutzinger, Christopher J. Peters, Zarah Abdullahi, Jason Crawte, Shona MacRae, Ayesha Noorani, Rachael Fels Elliott, Lawrence Bower, Paul A. Edwards, Simon Tavaré, Matthew Eldridge, Jan Bornschein, Maria Secrier, Yeng Ang, J. Robert O’Neill, Kasia Adamczuk
Julkaistu 2015Artigo -
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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Tekijä Jenny C. Taylor, Hilary C. Martin, Stefano Lise, John Broxholme, Jean‐Baptiste Cazier, Andy Rimmer, Alexander Kanapin, Gerton Lunter, Simon Fiddy, Chris Allan, A.R. Aricescu, Moustafa Attar, Christian Babbs, Jennifer Becq, David Beeson, Celeste Bento, P Bignell, Edward Blair, Veronica J. Buckle, Katherine R. Bull, Ondřej Cais, Holger Cario, Helen Chapel, Richard R. Copley, Richard J. Cornall, Jude Craft, Karin Dahan, Emma E. Davenport, Calliope A. Dendrou, Olivier Devuyst, Aimée L Fenwick, Jonathan Flint, Lars Fugger, Rodney D. Gilbert, Anne Goriely, Angie Green, Ingo H. Greger, Russell Grocock, Anja V. Gruszczyk, Robert Hastings, Edouard Hatton, Douglas R. Higgs, Adrian V. S. Hill, Chris Holmes, Malcolm F. Howard, Linda Hughes, Peter Humburg, David H. Johnson, Fredrik Karpe, Zoya Kingsbury, Usha Kini, Julian C. Knight, Jonathan Krohn, Sarah Lamble, Craig B. Langman, Lorne Lonie, Joshua Luck, Davis J. McCarthy, Simon J. McGowan, Mary Frances McMullin, Kerry A. Miller, Lisa Murray, Andrea H. Németh, M. Andrew Nesbit, David Nutt, Elizabeth Ormondroyd, Annette Oturai, Alistair T. Pagnamenta, Smita Y. Patel, Melanie J. Percy, Nayia Petousi, Paolo Piazza, Siân E. Piret, Guadalupe Polanco‐Echeverry, Niko Popitsch, Fiona Powrie, Christopher W. Pugh, Lynn Quek, Peter A. Robbins, Kathryn Robson, Alexandra Russo, Natasha Sahgal, Pauline A. van Schouwenburg, Anna Schuh, Earl D. Silverman, Alison Simmons, Per Soelberg Sørensen, Elizabeth Sweeney, John Taylor, Rajesh V. Thakker, Ian Tomlinson, Amy Trebes, Stephen R.F. Twigg, Holm H. Uhlig, Paresh Vyas, Tim J. Vyse, Steven A. Wall, Hugh Watkins, Michael P. Whyte, Lorna Witty
Julkaistu 2015Artigo
Työkalut:
Liittyvät aiheet
Biology
Genetics
Gene
Genome
Computational biology
Medicine
Cancer
DNA sequencing
Computer science
Internal medicine
Bacteria
Cancer research
Genotype
Leukemia
Lineage (genetic)
Mutation
Pathology
Somatic cell
Tuberculosis
Whole genome sequencing
Chronic lymphocytic leukemia
Engineering
Evolutionary biology
Gene expression
Genotyping
Horizontal gene transfer
Indel
Microbiology
Mycobacterium tuberculosis
Single-nucleotide polymorphism