Search Results - Scott E. Devine
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Small insertions and deletions (INDELs) in human genomes by Julienne M. Mullaney, Ryan E. Mills, W. Stephen Pittard, Scott E. Devine
Published 2010Revisão -
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Natural genetic variation caused by small insertions and deletions in the human genome by Ryan E. Mills, W. Stephen Pittard, Julienne M. Mullaney, Umar Farooq, Todd Creasy, Anup Mahurkar, David M. Kemeza, Daniel S. Strassler, Chris P. Ponting, Caleb Webber, Scott E. Devine
Published 2011Artigo -
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Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads by David Porubský, Peter Ebert, Peter A. Audano, Mitchell R. Vollger, William T. Harvey, Pierre Marijon, Jana Ebler, Katherine M. Munson, Melanie Sorensen, Arvis Sulovari, Marina Haukness, Maryam Ghareghani, Peter M. Lansdorp, Benedict Paten, Scott E. Devine, Ashley D. Sanders, Charles Lee, Mark Chaisson, Jan O. Korbel, Evan E. Eichler, Tobias Marschall
Published 2020Artigo -
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Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies by Xuefang Zhao, Ryan L. Collins, Wan‐Ping Lee, Alexandra M. Weber, Yukyung Jun, Qihui Zhu, Ben Weisburd, Yongqing Huang, Peter A. Audano, Harold Wang, Mark Walker, Chelsea Lowther, Jack Fu, Mark Gerstein, Scott E. Devine, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Mark Chaisson, Charles Lee, Ryan E. Mills, Harrison Brand, Michael E. Talkowski
Published 2021Artigo -
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Pulmonary Nontuberculous Mycobacterial Infection. A Multisystem, Multigenic Disease by Eva P. Szymanski, Janice M. Leung, Cedar Fowler, Carissa Haney, Amy P. Hsu, Fei Chen, Priya Duggal, Andrew J. Oler, Ryan McCormack, Eckhard R. Podack, Rebecca A. Drummond, Michail S. Lionakis, Sarah K. Browne, D. Rebecca Prevots, Michael R. Knowles, Gary Cutting, Xinyue Liu, Scott E. Devine, Claire M. Fraser, Hervé Tettelin, Kenneth N. Olivier, Steven M. Holland
Published 2015Artigo -
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High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios by Marta Byrska-Bishop, Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison Regier, André Corvelo, Wayne E. Clarke, Rajeeva Musunuri, Kshithija Nagulapalli, Susan Fairley, Alexi Runnels, Lara Winterkorn, Ernesto Lowy, Paul Flicek, Søren Germer, Harrison Brand, Ira M. Hall, Michael E. Talkowski, Giuseppe Narzisi, Michael C. Zody, Evan E. Eichler, Jan O. Korbel, Charles Lee, Tobias Marschall, Scott E. Devine, William T. Harvey, Weichen Zhou, Ryan E. Mills, Tobias Rausch, Sushant Kumar, Can Alkan, Fereydoun Hormozdiari, Zechen Chong, Yu Chen, Xiaofei Yang, Jiadong Lin, Mark Gerstein, Kai Ye, Qihui Zhu, Feyza Yilmaz, Chunlin Xiao
Published 2022Artigo -
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Haplotype-resolved diverse human genomes and integrated analysis of structural variation by Peter Ebert, Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubský, Marc Jan Bonder, Arvis Sulovari, Jana Ebler, Weichen Zhou, Rebecca Serra Mari, Feyza Yilmaz, Xuefang Zhao, PingHsun Hsieh, Joyce Lee, Sushant Kumar, Jiadong Lin, Tobias Rausch, Yu Chen, Jingwen Ren, Martín Santamarina, Wolfram Höps, Hufsah Ashraf, Nelson T. Chuang, Xiaofei Yang, Katherine M. Munson, Alexandra P. Lewis, Susan Fairley, Luke J. Tallon, Wayne E. Clarke, Anna O. Basile, Marta Byrska-Bishop, André Corvelo, Uday S. Evani, Tsung-Yu Lu, Mark Chaisson, Junjie Chen, Chong Li, Harrison Brand, Aaron M. Wenger, Maryam Ghareghani, William T. Harvey, Benjamin Raeder, Patrick Hasenfeld, Allison Regier, Haley Abel, Ira M. Hall, Paul Flicek, Oliver Stegle, Mark Gerstein, José M. C. Tubío, Zepeng Mu, Yang Li, Xinghua Shi, Alex Hastie, Kai Ye, Zechen Chong, Ashley D. Sanders, Michael C. Zody, Michael E. Talkowski, Ryan E. Mills, Scott E. Devine, Charles Lee, Jan O. Korbel, Tobias Marschall, Evan E. Eichler
Published 2021Artigo -
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An integrated map of structural variation in 2,504 human genomes by Peter H. Sudmant, Tobias Rausch, Eugene J. Gardner, Robert E. Handsaker, Alexej Abyzov, John Huddleston, Yan Zhang, Kai Ye, Goo Jun, Markus Hsi-Yang Fritz, Miriam K. Konkel, Ankit Malhotra, Adrian M. Stütz, Xinghua Shi, Francesco Paolo Casale, Jieming Chen, Fereydoun Hormozdiari, Gargi Dayama, Ken Chen, Maika Malig, Mark Chaisson, Klaudia Walter, Sascha Meiers, Seva Kashin, Erik Garrison, Adam Auton, Hugo Y. K. Lam, Xinmeng Jasmine Mu, Can Alkan, Danny Antaki, Taejeong Bae, Eliza Cerveira, Peter S. Chines, Zechen Chong, Laura Clarke, Elif Dal, Li Ding, Sarah B. Emery, Xian Fan, Madhusudan Gujral, Fatma Kahveci, Jeffrey M. Kidd, Yu Kong, Eric-Wubbo Lameijer, Shane McCarthy, Paul Flicek, Richard A. Gibbs, Gábor Marth, Christopher E. Mason, Androniki Menelaou, Donna M. Muzny, Bradley J. Nelson, Amina Noor, Nicholas F. Parrish, Matthew Pendleton, Andrew Quitadamo, Benjamin Raeder, Eric E. Schadt, Xian Mallory, Andreas Schlattl, Robert Sebra, Andrey A. Shabalin, Andreas Untergasser, Jerilyn A. Walker, Min Wang, Fuli Yu, Chengsheng Zhang, Jing Zhang, Xiangqun Zheng-Bradley, Wanding Zhou, Thomas Zichner, Jonathan Sebat, Mark A. Batzer, Steven A. McCarroll, Ryan E. Mills, Mark Gerstein, Ali Bashir, Oliver Stegle, Scott E. Devine, Charles Lee, Evan E. Eichler, Jan O. Korbel
Published 2015Artigo -
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Multi-platform discovery of haplotype-resolved structural variation in human genomes by Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, Ankit Malhotra, David Porubský, Tobias Rausch, Eugene J. Gardner, Oscar L. Rodriguez, Li Guo, Ryan L. Collins, Xian Fan, Jia Wen, Robert E. Handsaker, Susan Fairley, Zev Kronenberg, Xiangmeng Kong, Fereydoun Hormozdiari, Dillon Lee, Aaron M. Wenger, Alex Hastie, Danny Antaki, Peter A. Audano, Harrison Brand, Stuart Cantsilieris, Han Cao, Eliza Cerveira, Chong Chen, Xintong Chen, Chen-Shan Chin, Zechen Chong, Nelson T. Chuang, Christine Lambert, Deanna M. Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur R. Galeev, David U. Gorkin, Madhusudan Gujral, Victor Guryev, Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Jong Eun Lee, Joyce Lee, Wan‐Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine A. Viaud‐Martinez, Sascha Meiers, Katherine M. Munson, Fábio C. P. Navarro, Bradley J. Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy Wing Chun Pang, Yunjiang Qiu, Gabriel Rosanio, Xian Mallory, Adrian M. Stütz, Diana C.J. Spierings, Alistair Ward, AnneMarie E. Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy, Sergei Yakneen, Steven A. McCarroll, Goo Jun, Li Ding, Chong‐Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark Gerstein, Pui‐Yan Kwok, Peter M. Lansdorp, Gábor Marth, Jonathan Sebat, Xinghua Shi, Ali Bashir, Kai Ye, Scott E. Devine, Michael E. Talkowski, Ryan E. Mills, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Charles Lee
Published 2017Pré-impressão
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Biology
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Single-nucleotide polymorphism
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Haplotype
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DNA sequencing
Evolutionary biology
Genetic variation
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INDEL Mutation
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