نتائج البحث - Scott E. Devine
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The SIR2 gene family, conserved from bacteria to humans, functions in silencing, cell cycle progression, and chromosome stability. حسب Carrie Baker Brachmann, Joyce M. Sherman, Scott E. Devine, Ewan Cameron, Lorraine Pillus, Jef D. Boeke
منشور في 1995Artigo -
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The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology حسب Eugene J. Gardner, Vincent Kwok Lim Lam, Daniel Harris, Nelson T. Chuang, Emma C. Scott, W. Stephen Pittard, Ryan E. Mills, Scott E. Devine
منشور في 2017Artigo -
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Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs حسب Tsung-Yu Lu, Katherine M. Munson, Alexandra P. Lewis, Qihui Zhu, Luke J. Tallon, Scott E. Devine, Charles Lee, Evan E. Eichler, Mark Chaisson
منشور في 2021Artigo -
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Natural genetic variation caused by small insertions and deletions in the human genome حسب 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
منشور في 2011Artigo -
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Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads حسب 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
منشور في 2020Artigo -
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Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies حسب 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
منشور في 2021Artigo -
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Pulmonary Nontuberculous Mycobacterial Infection. A Multisystem, Multigenic Disease حسب 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
منشور في 2015Artigo -
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High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios حسب 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
منشور في 2022Artigo -
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Haplotype-resolved diverse human genomes and integrated analysis of structural variation حسب 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
منشور في 2021Artigo -
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An integrated map of structural variation in 2,504 human genomes حسب 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
منشور في 2015Artigo -
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Multi-platform discovery of haplotype-resolved structural variation in human genomes حسب 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
منشور في 2017Pré-impressão
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Genome
Computational biology
Genotype
Single-nucleotide polymorphism
1000 Genomes Project
Human genome
Indel
Structural variation
Haplotype
Reference genome
DNA sequencing
Evolutionary biology
Genetic variation
Cell biology
Human genetic variation
Sociology
Biochemistry
Cell nucleus
Computer science
Demography
Genomics
INDEL Mutation
Nuclear localization sequence
Nuclear transport
Population
Transposable element
Allele