Результати пошуку - Tim Fennell

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  1. 1
    ContEst: estimating cross-contamination of human samples in next-generation sequencing data

    ContEst: estimating cross-contamination of human samples in next-generation sequencing data за авторством Kristian Cibulskis, Aaron McKenna, Tim Fennell, Eric Banks, Mark A. DePristo, Gad Getz

    Опубліковано 2011
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  2. 2
    Fast and accurate kinship estimation using sparse SNPs in relatively large database searches

    Fast and accurate kinship estimation using sparse SNPs in relatively large database searches за авторством June Snedecor, Tim Fennell, Seth Stadick, Nils Homer, Joana Antunes, Kathryn M. Stephens, Cydne Holt

    Опубліковано 2022
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  3. 3
    The Sequence Alignment/Map format and SAMtools

    The Sequence Alignment/Map format and SAMtools за авторством Heng Li, Robert E. Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gábor Marth, Gonçalo R. Abecasis, Richard Durbin

    Опубліковано 2009
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  4. 4
    A framework for variation discovery and genotyping using next-generation DNA sequencing data

    A framework for variation discovery and genotyping using next-generation DNA sequencing data за авторством Mark A. DePristo, Eric Banks, Ryan Poplin, Kiran Garimella, Jared Maguire, Christopher Hartl, Anthony Philippakis, Guillermo del Angel, Manuel A. Rivas, Matt Hanna, Aaron McKenna, Tim Fennell, Andrew Kernytsky, Andrey Sivachenko, Kristian Cibulskis, Stacey Gabriel, David Altshuler, Mark J. Daly

    Опубліковано 2011
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  5. 5
    Scaling accurate genetic variant discovery to tens of thousands of samples

    Scaling accurate genetic variant discovery to tens of thousands of samples за авторством Ryan Poplin, Valentín Ruano-Rubio, Mark A. DePristo, Tim Fennell, Mauricio O. Carneiro, Géraldine A. Van der Auwera, David E. Kling, Laura D. Gauthier, Ami Levy‐Moonshine, David Roazen, Khalid Shakir, Joel Thibault, Sheila Chandran, Chris Whelan, Monkol Lek, Stacey Gabriel, Mark J. Daly, Ben Neale, Daniel G. MacArthur, Eric Banks

    Опубліковано 2017
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  6. 6
    Exome Sequencing,<i>ANGPTL3</i>Mutations, and Familial Combined Hypolipidemia

    Exome Sequencing,<i>ANGPTL3</i>Mutations, and Familial Combined Hypolipidemia за авторством Kiran Musunuru, James P. Pirruccello, Ron Do, Gina M. Peloso, Candace Guiducci, Carrie Sougnez, Kiran Garimella, Sheila Fisher, Justin Abreu, Andrew J. Barry, Tim Fennell, Eric Banks, Lauren Ambrogio, Kristian Cibulskis, Andrew Kernytsky, Elena González, Nicholas Rudzicz, James C. Engert, Mark A. DePristo, Mark J. Daly, Jonathan C. Cohen, Helen H. Hobbs, David Altshuler, Gustav Schonfeld, Stacey Gabriel, Pin Yue, Sekar Kathiresan

    Опубліковано 2010
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  7. 7
    Drug-sensitive<i>FGFR2</i>mutations in endometrial carcinoma

    Drug-sensitive<i>FGFR2</i>mutations in endometrial carcinoma за авторством Amit Dutt, Helga B. Salvesen, Tzu-Hsiu Chen, Alex H. Ramos, Robert C. Onofrio, Charlie Hatton, Richard Nicoletti, Wendy Winckler, Rupinder Grewal, Megan Hanna, Nicolas Wyhs, Liuda Ziaugra, Daniel J. Richter, Jone Trovik, Ingeborg B. Engelsen, Ingunn M. Stefansson, Tim Fennell, Kristian Cibulskis, Michael C. Zody, Lars A. Akslen, Stacey B. Gabriel, Kwok‐Kin Wong, William R. Sellers, Matthew Meyerson, Heidi Greulich

    Опубліковано 2008
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  8. 8
    A polygenic burden of rare disruptive mutations in schizophrenia

    A polygenic burden of rare disruptive mutations in schizophrenia за авторством Shaun Purcell, Jennifer L. Moran, Menachem Fromer, Douglas M. Ruderfer, Nadia Solovieff, Panos Roussos, Colm Ó'Dúshláine, Kimberly Chambert, Sarah E. Bergen, Anna K. Kähler, Laramie E. Duncan, Eli Stahl, Giulio Genovese, Esperanza Fernández, Mark O. Collins, Noboru H. Komiyama, Jyoti S. Choudhary, Patrik K. E. Magnusson, Eric Banks, Khalid Shakir, Kiran Garimella, Tim Fennell, Mark A. DePristo, Seth G. N. Grant, Stephen J. Haggarty, Stacey Gabriel, Edward M. Scolnick, Eric S. Lander, Christina M. Hultman, Patrick F. Sullivan, Steven A. McCarroll, Pamela Sklar

    Опубліковано 2014
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  9. 9
    Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

    Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease за авторством Manuel A. Rivas, Mélissa Beaudoin, Agnès Gardet, Christine Stevens, Yashoda Sharma, Hu Zhang, Gabrielle Boucher, Stephan Ripke, David Ellinghaus, Noël P. Burtt, Tim Fennell, Andrew Kirby, Anna Latiano, Philippe Goyette, Todd J. Green, Jonas Halfvarson, Talin Haritunians, Joshua M. Korn, Finny G. Kuruvilla, Caroline Lagacé, Benjamin M. Neale, Ken Sin Lo, L. Philip Schumm, Leif Törkvist, Marla C. Dubinsky, Steven R. Brant, Mark S. Silverberg, Richard H. Duerr, David Altshuler, Stacey Gabriel, Guillaume Lettre, André Franke, Mauro D’Amato, Dermot McGovern, Judy H. Cho, John D. Rioux, Ramnik J. Xavier, Mark J. Daly

    Опубліковано 2011
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  10. 10
    Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy

    Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy за авторством Jordi Barretina, Barry S. Taylor, Shantanu Banerji, Alexis Ramos, Mariana Lagos‐Quintana, Penelope DeCarolis, Kinjal Shah, Nicholas D. Socci, Barbara A. Weir, Alan L. Ho, Derek Y. Chiang, Boris Reva, Craig H. Mermel, Gad Getz, Yevgenyi Antipin, Rameen Beroukhim, John E. Major, Charlie Hatton, Richard Nicoletti, Megan Hanna, Ted Sharpe, Tim Fennell, Kristian Cibulskis, Robert C. Onofrio, Tsuyoshi Saito, Neerav Shukla, Christopher Lau, Sven Nelander, Serena J. Silver, Carrie Sougnez, Agnès Viale, Wendy Winckler, Robert G. Maki, Levi A. Garraway, Alex E. Lash, Heidi Greulich, David E. Root, William R. Sellers, Gary K. Schwartz, Cristina R. Antonescu, Eric S. Lander, Harold Varmus, Marc Ladanyi, Chris Sander, Matthew Meyerson, Samuel Singer

    Опубліковано 2010
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  11. 11
    Patterns and rates of exonic de novo mutations in autism spectrum disorders

    Patterns and rates of exonic de novo mutations in autism spectrum disorders за авторством Benjamin M. Neale, Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo, Chiao‐Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov, Paz Polak, Seungtai Yoon, Jared Maguire, Emily L. Crawford, Nicholas G. Campbell, Evan Geller, Otto Valladares, Chad Schafer, Han Liu, Tuo Zhao, Guiqing Cai, Jayon Lihm, Ruth Dannenfelser, Omar Jabado, Zuleyma Peralta, Uma Nagaswamy, Donna M. Muzny, Jeffrey G. Reid, Irene Newsham, Yuanqing Wu, Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly

    Опубліковано 2012
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  12. 12
    Somatic mutations affect key pathways in lung adenocarcinoma

    Somatic mutations affect key pathways in lung adenocarcinoma за авторством Li Ding, Gad Getz, David A. Wheeler, Elaine R. Mardis, Michael D. McLellan, Kristian Cibulskis, Carrie Sougnez, Heidi Greulich, Donna M. Muzny, Margaret Morgan, Lucinda Fulton, Robert S. Fulton, Qunyuan Zhang, Michael C. Wendl, Michael S. Lawrence, David E. Larson, Ken Chen, David J. Dooling, Aniko Sabo, Alicia Hawes, Hua Shen, Shalini N. Jhangiani, Lora Lewis, Otis Hall, Yiming Zhu, Tittu Mathew, Yanru Ren, Jiqiang Yao, Steven E. Scherer, Kerstin Clerc, Ginger Metcalf, Brian Ng, Aleksandar Milosavljevic, Manuel L. Gonzalez‐Garay, John R. Osborne, Rick Meyer, Xiaoqi Shi, Yuzhu Tang, Daniel C. Koboldt, Ling Lin, Rachel M. Abbott, Tracie L. Miner, Craig Pohl, Ginger Fewell, Carrie A. Haipek, Heather K. Schmidt, Brian H. Dunford-Shore, Aldi T. Kraja, Seth D. Crosby, Christopher S. Sawyer, Tammi L. Vickery, Sacha N Sander, Jody S. Robinson, Wendy Winckler, Jennifer Baldwin, Lucian R. Chirieac, Amit Dutt, Tim Fennell, Megan Hanna, Bruce E. Johnson, Robert C. Onofrio, Roman K. Thomas, Giovanni Tonon, Barbara A. Weir, Xiao‐Jun Zhao, Liuda Ziaugra, Michael C. Zody, Thomas J. Giordano, Mark B. Orringer, Jack A. Roth, Margaret R. Spitz, Ignacio I. Wistuba, Bradley A. Ozenberger, Peter J. Good, Andrew C. Chang, David G. Beer, Mark A. Watson, Marc Ladanyi, Stephen Broderick, Akihiko Yoshizawa, William D. Travis, William Pao, Michael A. Province, George M. Weinstock, Harold Varmus, Stacey Gabriel, Eric S. Lander, Richard A. Gibbs, Matthew Meyerson, Richard K. Wilson

    Опубліковано 2008
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  13. 13
    Demographic history and rare allele sharing among human populations

    Demographic history and rare allele sharing among human populations за авторством Simon Gravel, Brenna M. Henn, Ryan N. Gutenkunst, Amit Indap, Gábor Marth, Andrew G. Clark, Fuli Yu, Richard A. Gibbs, Carlos D. Bustamante, David L. Altshuler, Richard Durbin, Gonçalo R. Abecasis, David Bentley, Aravinda Chakravarti, Andrew G. Clark, Francis S. Collins, Francisco M. De La Vega, Peter Donnelly, Michael D. Miller, Paul Flicek, Stacey Gabriel, Richard A. Gibbs, Bartha Maria Knoppers, Eric S. Lander, Hans Lehrach, Elaine R. Mardis, Gil McVean, Debbie A. Nickerson, Leena Peltonen, Alan J. Schafer, Stephen T. Sherry, Jun Wang, Richard K. Wilson, Richard A. Gibbs, David Rio Deiros, Mike Metzker, Donna M. Muzny, Jeff Reid, David A. Wheeler, Jun Wang, Jingxiang Li, Min Jian, Guoqing Li, Ruiqiang Li, Huiqing Liang, Geng Tian, Bó Wáng, Jian Wang, Wei Wang, Huanming Yang, Xiuqing Zhang, Huisong Zheng, Eric S. Lander, David L. Altshuler, Lauren Ambrogio, Toby Bloom, Kristian Cibulskis, Tim Fennell, Stacey Gabriel, David B. Jaffe, Erica Shefler, Carrie Sougnez, David Bentley, Niall Gormley, Sean Humphray, Zoya Kingsbury, Paula Koko-Gonzales, Jennifer Stone, Kevin McKernan, Gina L. Costa, Jeffry K. Ichikawa, Clarence Lee, Ralf Sudbrak, Hans Lehrach, Tatiana Borodina, Andreas Dahl, Alexey N. Davydov, P Marquardt, Florian Mertes, Wilfiried Nietfeld, Philip Rosenstiel, Stefan Schreiber, Aleksey V. Soldatov, Bernd Timmermann, Marius Tolzmann, Michael D. Miller, Jason P. Affourtit, Dana Ashworth, Said Attiya, Melissa Bachorski, Eli Buglione, Adam Burke, Amanda Caprio, Christopher Celone, Andrew G. Clark, David Conners, Brian Desany, Lisa Gu, Lorri Guccione, Kalvin Kao

    Опубліковано 2011
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  14. 14
    Integrated genomic analyses of ovarian carcinoma

    Integrated genomic analyses of ovarian carcinoma за авторством Debra Bell, Andrew Berchuck, Michael J. Birrer, Jeremy Chien, D. W. Cramer, Fanny Dao, Rajiv Dhir, Philip J. DiSaia, Hani Gabra, Pat Glenn, A. K. Godwin, Jenny Gross, L Hartmann, Mei Huang, David G. Huntsman, Mary Iacocca, Marcin Imieliński, Steve E. Kalloger, Beth Y. Karlan, Douglas A. Levine, G.B. Mills, Carl Morrison, David G. Mutch, Narciso Olvera, Sandra Oršulić, Kay J. Park, Nicholas J. Petrelli, Brenda Rabeno, Janet S. Rader, Branimir I. Šikić, Karen Smith‐McCune, Anil K. Sood, David D.L. Bowtell, Robert Penny, Joseph R. Testa, Kuo-Ching Chang, Huyen Dinh, Jennifer Drummond, Gerald Fowler, Preethi H. Gunaratne, Alicia Hawes, C. Kovar, Lora Lewis, M. B. Morgan, Irene Newsham, Jireh Santibanez, J. G. Reid, Lisa R. Treviño, Y. Q. Wu, M. Wang, Donna M. Muzny, David A. Wheeler, Richard A. Gibbs, Gaddy Getz, Michael S. Lawrence, Kristian Cibulskis, Andrey Sivachenko, Carrie Sougnez, Douglas Voet, Jennifer Wilkinson, Theodora Bloom, Kristin Ardlie, Tim Fennell, Jennifer Baldwin, Stacey Gabriel, Eric S. Lander, Li Ding, Robert S. Fulton, Daniel C. Koboldt, Michael D. McLellan, Todd Wylie, John R. Walker, M. O'Laughlin, David J. Dooling, Lucinda Fulton, Ryan Abbott, Nathan D. Dees, Q. Zhang, Cyriac Kandoth, Michael C. Wendl, William Schierding, Dejun Shen, Christopher Harris, Heather K. Schmidt, Joelle Kalicki, Kim D. Delehaunty, Catrina C. Fronick, Ryan Demeter, Lisa L. Cook, John W. Wallis, Liwei Lin, Vincent Magrini, James S. Hodges, James M. Eldred, S. M. Smith, Craig Pohl, Fabio Vandin, Benjamin J. Raphael, George M. Weinstock, Elaine R. Mardis

    Опубліковано 2011
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  15. 15
    Comprehensive genomic characterization defines human glioblastoma genes and core pathways

    Comprehensive genomic characterization defines human glioblastoma genes and core pathways за авторством Roger E. McLendon, Allan H. Friedman, D D Bigner, Erwin G. Van Meir, Daniel J. Brat, Gena M. Mastrogianakis, Jeffrey J. Olson, Tom Mikkelsen, Norman L. Lehman, Ken Aldape, W.K. Alfred Yung, Oliver Bögler, John N. Weinstein, Scott Vandenberg, Mitchel S. Berger, Michael D. Prados, Donna M. Muzny, Margaret Morgan, Stephen W. Scherer, Aniko Sabo, Lynn Nazareth, Lora Lewis, Otis Hall, Yiming Zhu, Yanru Ren, Omar Alvi, Jiqiang Yao, Alicia Hawes, Shalini N. Jhangiani, Gerald Fowler, Anthony San Lucas, Christie Kovar, Andrew Cree, Huyen Dinh, Jireh Santibanez, Vandita Joshi, Manuel L. Gonzalez‐Garay, Christopher A. Miller, Aleksandar Milosavljevic, L A Donehower, David A. Wheeler, Richard A. Gibbs, Kristian Cibulskis, Carrie Sougnez, Tim Fennell, Scott Mahan, Jane Wilkinson, Liuda Ziaugra, Robert C. Onofrio, Toby Bloom, Robert Nicol, Kristin Ardlie, Jennifer Baldwin, Stacey Gabriel, Eric S. Lander, Jun Li, Robert S. Fulton, Michael D. McLellan, John Wallis, David E. Larson, Xiaoqi Shi, Rachel M. Abbott, Lucinda Fulton, Ken Chen, Daniel C. Koboldt, Michael C. Wendl, Rick Meyer, Yuzhu Tang, Ling Lin, John R. Osborne, Brian H. Dunford-Shore, Tracie L. Miner, Kim D. Delehaunty, Chris Markovic, G.M. Swift, William Courtney, Craig Pohl, Scott Abbott, Amy Hawkins, Shin Leong, Carrie A. Haipek, Heather K. Schmidt, Maddy Wiechert, Tammi L. Vickery, S. P. Scott, David J. Dooling, Asif Chinwalla, George M. Weinstock, Elaine R. Mardis, Richard K. Wilson, Gad Getz, Wendy Winckler, Roel G.W. Verhaak, Michael S. Lawrence, Michael O’Kelly, Jim Robinson, Gabriele Alexe, Rameen Beroukhim, Scott L. Carter, Derek Y. Chiang

    Опубліковано 2008
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