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CONSERTING: integrating copy-number analysis with structural-variation detection de réir Xiang Chen, Pankaj Gupta, Jianmin Wang, Joy Nakitandwe, Kathryn G. Roberts, James Dalton, Matthew Parker, Samir Patel, Linda Holmfeldt, Debbie Payne, John Easton, Jing Ma, Michael Rusch, Gang Wu, Aman Patel, Suzanne J. Baker, Michael A. Dyer, Sheila Shurtleff, Stephen Espy, Stanley Pounds, James R. Downing, David W. Ellison, Charles G. Mullighan, Jinghui Zhang

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Single-molecule analysis reveals widespread structural variation in multiple myeloma de réir Aditya Gupta, Michael Place, Steven Goldstein, Deepayan Sarkar, Shiguo Zhou, Konstantinos Potamousis, Jaehyup Kim, Claire Flanagan, Yang Li, Michael A. Newton, Natalie S. Callander, Peiman Hematti, Emery H. Bresnick, Jian Ma, Fotis Asimakopoulos, David C. Schwartz

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Detection of Genomic Structural Variants from Next-Generation Sequencing Data de réir Lorenzo Tattini, Romina D’Aurizio, Alberto Magi

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BreakDancer: Identification of Genomic Structural Variation from Paired‐End Read Mapping de réir Xian Fan, Travis E. Abbott, David E. Larson, Ken Chen

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Human Structural Variation: Mechanisms of Chromosome Rearrangements de réir Brooke Weckselblatt, M. Katharine Rudd

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Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation de réir Harrison Brand, Ryan L. Collins, Carrie Hanscom, Jill A. Rosenfeld, Vamsee Pillalamarri, Matthew R. Stone, Fontina Kelley, Tamara Mason, Lauren Margolin, Stacey Eggert, Elyse Mitchell, Jennelle C. Hodge, James F. Gusella, Stephan Sanders, Michael E. Talkowski

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A large and diverse collection of bovine genome sequences from the Canadian Cattle Genome Project de réir Paul Stothard, Xiaoping Liao, Adriano S. Arantes, M. De Pauw, Colin J. Coros, Graham Plastow, Mehdi Sargolzaei, John J. Crowley, J. A. Basarab, Flávio S. Schenkel, S. S. Moore, Stephen P. Miller

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Spontaneous sequence duplication within an open reading frame of the pneumococcal type 3 capsule locus causes high‐frequency phase variation de réir Richard Waite, J. K. Struthers, Christopher G. Dowson

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Genome-Wide Study of Structural Variants in Bovine Holstein, Montbéliarde and Normande Dairy Breeds de réir Mekki Boussaha, Diane Esquerré, Johanna Barbieri, Anis Djari, Alain Pinton, Rabia Letaïef, Gérald Salin, Fréderic Escudié, Alain Roulet, Sébastien Fritz, Franck Samson, Cécile Grohs, Maria Bernard, Christophe Klopp, Didier Boichard, Dominique Rocha

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An integrated map of structural variation in 2,504 human genomes de réir 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

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Whole Genome Distribution and Ethnic Differentiation of Copy Number Variation in Caucasian and Asian Populations de réir Jian Li, Tie‐Lin Yang, Liang Wang, Han Yan, Yin‐Ping Zhang, Yan Guo, Feng Pan, Zhixin Zhang, Yumei Peng, Qi Zhou, Wei‐Guang Li, Xue-Zhen Zhu, Hongyi Deng, Shawn Levy, Christopher J. Papasian, Betty M. Drees, James J. Hamilton, Robert R. Recker, Jing Cheng, Hong‐Wen Deng

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Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly de réir Yingrui Li, Hancheng Zheng, Ruibang Luo, Honglong Wu, Hongmei Zhu, Ruiqiang Li, Hongzhi Cao, Boxin Wu, Shujia Huang, Haojing Shao, Hanzhou Ma, Fan Zhang, Shuijian Feng, Wei Zhang, Hongli Du, Geng Tian, Jingxiang Li, Xiuqing Zhang, Songgang Li, Lars Bolund, Karsten Kristiansen, Adam J. de Smith, Alexandra I. F. Blakemore, Lachlan Coin, Huanming Yang, Jian Wang, Jun Wang

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Prescribing Personalized Nutrition for Cardiovascular Health: Are We Ready? de réir Shanil Juma, Victorine Imrhan, Parakat Vijayagopal, Chandan Prasad

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Sequence-based characterization of structural variation in the mouse genome de réir Binnaz Yalcin, Kim Wong, Avigail Agam, Martin Goodson, Thomas Keane, Xiangchao Gan, Christoffer Nellåker, Leo Goodstadt, Jérôme Nicod, Amarjit Bhomra, Polinka Hernandez-Pliego, Helen Whitley, James Cleak, Rebekah Dutton, Deborah Janowitz, Richard Mott, David J. Adams, Jonathan Flint

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Decoding complex patterns of genomic rearrangement in hepatocellular carcinoma de réir Julio Fernandez-Banet, Nikki P. Lee, Kin Chan, Huan Gao, Xiao Liu, Wing‐Kin Sung, Winnie Tan, Sheung Tat Fan, Ronnie T.P. Poon, Shiyong Li, Keith A. Ching, Paul A. Rejto, Mao Mao, Zhengyan Kan

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Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches de réir Haley Abel, Eric J. Duncavage

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Genome-Wide Mapping of Copy Number Variation in Humans: Comparative Analysis of High Resolution Array Platforms de réir Rajini Haraksingh, Alexej Abyzov, Mark Gerstein, Alexander E. Urban, M Snyder

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Evolution of variation in presence and absence of genes in bacterial pathways de réir Andrew Francis, Mark M. Tanaka

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Tandem Repeats and G-Rich Sequences Are Enriched at Human CNV Breakpoints de réir Promita Bose, Karen Hermetz, Karen N. Conneely, M. Katharine Rudd

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Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders de réir Harrison Brand, Vamsee Pillalamarri, Ryan L. Collins, Stacey Eggert, Colm Ó'Dúshláine, Ellen B. Braaten, Matthew R. Stone, Kimberly Chambert, Nathan D. Doty, Carrie Hanscom, Jill A. Rosenfeld, Hillary L. Ditmars, Jessica E. Blais, Ryan E. Mills, Charles Lee, James F. Gusella, Steven A. McCarroll, Jordan W. Smoller, Michael E. Talkowski, Alysa E. Doyle

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