Resultats de la cerca - Martin Pollard

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  1. 1
    Long reads: their purpose and place

    Long reads: their purpose and place per Martin Pollard, Deepti Gurdasani, Alexander J. Mentzer, Tarryn Porter, Manjinder S. Sandhu

    Publicat 2018
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  2. 2
    Twelve years of SAMtools and BCFtools

    Twelve years of SAMtools and BCFtools per Petr Danecek, James Bonfield, Jennifer Liddle, John Marshall, Valeriu Ohan, Martin Pollard, Andrew Whitwham, Thomas Keane, Shane McCarthy, Robert M. Davies, Heng Li

    Publicat 2021
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  3. 3
    Deep Roots for Aboriginal Australian Y Chromosomes

    Deep Roots for Aboriginal Australian Y Chromosomes per Anders Bergström, Nano Nagle, Yuan Chen, Shane McCarthy, Martin Pollard, Qasim Ayub, Stephen Wilcox, Leah Wilcox, Roland A.H. van Oorschot, Peter McAllister, Lesley Williams, Yali Xue, R. John Mitchell, Chris Tyler‐Smith

    Publicat 2016
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  4. 4
    Very low-depth whole-genome sequencing in complex trait association studies

    Very low-depth whole-genome sequencing in complex trait association studies per Arthur Gilly, Lorraine Southam, Dániel Süveges, Karoline Kuchenbaecker, Rachel Moore, Giorgio Melloni, Konstantinos Hatzikotoulas, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Jeremy Schwartzentruber, Petr Danecek, Britt Kilian, Martin Pollard, Xiangyu Ge, Emmanouil Tsafantakis, George Dedoussis, Eleftheria Zeggini

    Publicat 2018
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  5. 5
    Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

    Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7 per Yang Luo, Katrina M. de Lange, Luke Jostins, Loukas Moutsianas, Joshua C. Randall, Nicholas A. Kennedy, Christopher A Lamb, Shane McCarthy, Tariq Ahmad, Cathryn Edwards, Eva Serra, Ailsa Hart, C J Hawkey, John Mansfield, Craig Mowat, William G. Newman, Sam Nichols, Martin Pollard, Jack Satsangi, Alison Simmons, Mark Tremelling, Holm H. Uhlig, David C. Wilson, James Lee, Natalie J. Prescott, Charlie W. Lees, Christopher G. Mathew, Miles Parkes, Jeffrey C. Barrett, Carl A. Anderson

    Publicat 2017
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  6. 6
    The African Genome Variation Project shapes medical genetics in Africa

    The African Genome Variation Project shapes medical genetics in Africa per Deepti Gurdasani, Tommy Carstensen, Fasil Tekola‐Ayele, Luca Pagani, Ioanna Tachmazidou, Konstantinos Hatzikotoulas, Savita Karthikeyan, Louise Iles, Martin Pollard, Ananyo Choudhury, Graham R. S. Ritchie, Yali Xue, Jennifer L. Asimit, Rebecca N. Nsubuga, Elizabeth Young, Cristina Pomilla, Katja Kivinen, Kirk A. Rockett, Anatoli Kamali, Ayo P. Doumatey, Gershim Asiki, Janet Seeley, Fatoumatta Sisay-Joof, Muminatou Jallow, Stephen Tollman, Ephrem Mekonnen, Rosemary Ekong, Tamiru Oljira, Neil Bradman, Kalifa Bojang, Michèle Ramsay, Adebowale Adeyemo, Endashaw Bekele, Ayesha A. Motala, Shane A. Norris, Fraser Pirie, Pontiano Kaleebu, Dominic Kwiatkowski, Chris Tyler‐Smith, Charles N. Rotimi, Eleftheria Zeggini, Manjinder S. Sandhu

    Publicat 2014
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  7. 7
    Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa

    Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa per Deepti Gurdasani, Tommy Carstensen, Segun Fatumo, Guanjie Chen, Chris S. Franklin, Javier Prado-Martinez, Heleen Bouman, Federico Abascal, Marc Haber, Ioanna Tachmazidou, Iain Mathieson, Kenneth Ekoru, Marianne K. DeGorter, Rebecca N. Nsubuga, Chris Finan, Eleanor Wheeler, Li Chen, D.N. Cooper, Stephan Schiffels, Yuan Chen, Graham R. S. Ritchie, Martin Pollard, Mary D Fortune, Alexander J. Mentzer, Erik Garrison, Anders Bergström, Konstantinos Hatzikotoulas, Adebowale Adeyemo, Ayo P. Doumatey, Heather Elding, Louise V. Wain, Georg Ehret, Paul L. Auer, Charles Kooperberg, Alexander P. Reiner, Nora Franceschini, Dermot Maher, Stephen B. Montgomery, Carl Kadie, Chris Widmer, Yali Xue, Janet Seeley, Gershim Asiki, Anatoli Kamali, Elizabeth Young, Cristina Pomilla, Nicole Soranzo, Eleftheria Zeggini, Fraser Pirie, Andrew P. Morris, David Heckerman, Chris Tyler‐Smith, Ayesha A. Motala, Charles N. Rotimi, Pontiano Kaleebu, Inês Barroso, Manj S. Sandhu

    Publicat 2019
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  8. 8
    The DNA sequence and comparative analysis of human chromosome 5

    The DNA sequence and comparative analysis of human chromosome 5 per Jeremy Schmutz, Joel Martin, Astrid Terry, Olivier Couronne, Jane Grimwood, Steve Lowry, Laurie Gordon, Duncan Scott, Gary Xie, Wayne Huang, Uffe Hellsten, Mary Bao Tran-Gyamfi, Xinwei She, Shyam Prabhakar, Andrea Aerts, Michael R. Altherr, Eva Bajorek, Stacey Black, Elbert Branscomb, Chenier Caoile, Jean F. Challacombe, Yee Man Chan, Mirian Denys, John C. Detter, Julio Escobar, Dave Flowers, Dea Fotopulos, Tijana Glavina, María Gómez, Eidelyn Gonzales, David Goodstein, Igor V. Grigoriev, Matthew Groza, Nancy Hammon, Trevor Hawkins, Lauren E. Haydu, Sanjay Israni, Jamie Jett, Kristen Kadner, Heather Kimball, Arthur Kobayashi, Frederick Lopez, Yunian Lou, Diego Martinez, Catherine Medina, Jenna Morgan, Richard D. Nandkeshwar, James P. Noonan, Sam Pitluck, Martin Pollard, Paul Predki, James R. Priest, Lucı́a Ramı́rez, James Retterer, Álex Rodríguez, Stephanie Rogers, Asaf Salamov, Angelica Salazar, Nina Thayer, Hope Tice, Ming Jer Tsai, Anna Ustaszewska, Nu Vo, Jeremy Wheeler, Kevin Wu, Joan Yang, Mark Dickson, Jan‐Fang Cheng, Evan E. Eichler, Anne Olsen, L Pennacchio, Daniel S. Rokhsar, Paul Richardson, Susan Lucas, R Myers, Edward M. Rubin

    Publicat 2004
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  9. 9
    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing per Alejandro Sifrim, Marc‐Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H. Al Turki, Bernard Thienpont, Jeremy F. McRae, Tomas Fitzgerald, Tarjinder Singh, G. Jawahar Swaminathan, Elena Prigmore, Diana Rajan, Hashim Abdul‐Khaliq, Siddharth Banka, Ulrike Bauer, Jamie Bentham, Felix Berger, Shoumo Bhattacharya, Frances Bu’Lock, Natalie Canham, Irina-Gabriela Colgiu, Catherine Cosgrove, Helen Cox, Ingo Daehnert, Allan Daly, John Danesh, Alan Fryer, Marc Gewillig, Emma Hobson, Kirstin Hoff, Tessa Homfray, Anne-Karin Kahlert, Ami Ketley, Hans-Heiner Kramer, Katherine Lachlan, Anne Katrin Lampe, Jacoba Louw, Ashok Kumar Manickara, Dorin Manase, Karen McCarthy, Kay Metcalfe, Carmel Moore, Ruth Newbury‐Ecob, Seham Osman Babiker Omer, Willem H. Ouwehand, Soo‐Mi Park, Michael Parker, Thomas Pickardt, Martin Pollard, Leema Robert, David J. Roberts, Jennifer Sambrook, Kerry Setchfield, Brigitte Stiller, Chris Thornborough, Okan Toka, Hugh Watkins, Denise Williams, Michael Wright, Seema Mital, Piers E.F. Daubeney, Bernard Keavney, Judith Goodship, Riyadh Mahdi Abu-Sulaiman, Sabine Klaassen, Caroline F. Wright, Helen V. Firth, Jeffrey C. Barrett, Koenraad Devriendt, David Fitzpatrick, J. David Brook, Matthew E. Hurles

    Publicat 2016
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  10. 10
    A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

    A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis per Manuel A. Rivas, Daniel B. Graham, Patrick Sulem, Christine Stevens, A. Nicole Desch, Philippe Goyette, Daníel F. Guðbjartsson, Ingileif Jónsdóttir, Unnur Þorsteinsdóttir, Frauke Degenhardt, Sören Mucha, Mitja Kurki, Dalin Li, Mauro D’Amato, Vito Annese, Séverine Vermeire, Rinse K. Weersma, Jonas Halfvarson, Paulina Paavola–Sakki, Maarit Lappalainen, Monkol Lek, Beryl B. Cummings, Taru Tukiainen, Talin Haritunians, Leena Halme, Lotta L. E. Koskinen, Ashwin N. Ananthakrishnan, Yang Luo, Graham Heap, Marijn C. Visschedijk, Jeffrey C. Barrett, Kim de Lange, Cathryn Edwards, AL Hart, C J Hawkey, Luke Jostins, Nicholas A. Kennedy, Christopher A Lamb, James Lee, Charlie W. Lees, John Mansfield, Christopher G. Mathew, C. Mowatt, William G. Newman, Elaine Nimmo, Miles Parkes, Martin Pollard, Natalie J. Prescott, Jessica Randall, Daniel L Rice, Jack Satsangi, Alison Simmons, Mark Tremelling, Holm H. Uhlig, David C. Wilson, Clara Abraham, J ACHKAR, Alain Bitton, Gabrielle Boucher, Kenneth Croitoru, Phil Fleshner, Jürgen Glas, Subra Kugathasan, Johan Van Limbergen, Raquel Milgrom, Deborah D. Proctor, Miguel Regueiro, L. Philip Schumm, Yashoda Sharma, Joanne M. Stempak, Stephan R. Targan, M. H. Wang, Daniel G. MacArthur, Benjamin M. Neale, Tariq Ahmad, Carl A. Anderson, Steven R. Brant, Richard H. Duerr, Mark S. Silverberg, Judy H. Cho, Aarno Palotie, Päivi Saavalainen, Kimmo Kontula, Martti Färkkilâ, Dermot McGovern, André Franke, Kāri Stefánsson, John D. Rioux, Ramnik J. Xavier, Mark J. Daly

    Publicat 2016
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  11. 11
    The sequence and analysis of duplication-rich human chromosome 16

    The sequence and analysis of duplication-rich human chromosome 16 per Joel Martin, Cliff Han, Laurie Gordon, Astrid Terry, Shyam Prabhakar, Xinwei She, Gary Xie, Uffe Hellsten, Yee Man Chan, Michael R. Altherr, Olivier Couronne, Andrea Aerts, Eva Bajorek, Stacey Black, Heather Blumer, Elbert Branscomb, Nancy C. Brown, William Bruno, Judith M. Buckingham, David F. Callen, Connie S. Campbell, Mary L. Campbell, E.W. Campbell, Chenier Caoile, Jean F. Challacombe, Leslie Chasteen, Olga Chertkov, Han Chu, Mari Christensen, Lynn M. Clark, Judith D. Cohn, Mirian Denys, John C. Detter, Mark Dickson, Mira Dimitrijevic-Bussod, Julio Escobar, Joseph J. Fawcett, Dave Flowers, Dea Fotopulos, Tijana Glavina, María Lucía Gutiérrez Gómez, Eidelyn Gonzales, David Goodstein, Lynne Goodwin, Deborah L. Grady, Igor V. Grigoriev, Matthew Groza, Nancy Hammon, Trevor Hawkins, Lauren E. Haydu, C.E. Hildebrand, Wayne Huang, Sanjay Israni, Jamie Jett, Phillip B. Jewett, Kristen Kadner, Heather Kimball, Arthur Kobayashi, Marie-Claude Krawczyk, Tina Leyba, Jonathan L. Longmire, Frederick Lopez, Yunian Lou, Steve Lowry, Thom Ludeman, Chitra Manohar, Graham A. Mark, Kimberly L. Mcmurray, Linda Meincke, Jenna Morgan, Robert K. Moyzis, Mark Mundt, A. Christine Munk, Richard D. Nandkeshwar, Sam Pitluck, Martin Pollard, Paul Predki, B. Parson-Quintana, Lucı́a Ramı́rez, Sam Rash, James Retterer, Darrell Ricke, Donna L. Robinson, Álex Rodríguez, Asaf Salamov, Elizabeth Saunders, Duncan Scott, Timothy Shough, Raymond L. Stallings, Malinda Stalvey, Robert Sutherland, Roxanne Tapia, Judith G. Tesmer, Nina Thayer, Linda S. Thompson, Hope Tice, David C. Torney, Mary Bao Tran-Gyamfi, Ming Jer Tsai, Levy Ulanovsky

    Publicat 2004
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