Výsledky vyhledávání - Anna O. Basile

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  1. 1
    Informatics and machine learning to define the phenotype

    Informatics and machine learning to define the phenotype Autor Anna O. Basile, Marylyn D. Ritchie

    Vydáno 2018
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  2. 2
    High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

    High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios Autor 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

    Vydáno 2021
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  3. 3
    Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state

    Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state Autor Fahad Paryani, Ji‐Sun Kwon, Christopher Ng, Kelly Jakubiak, Nacoya Madden, Kenneth Ofori, Alice Tang, Hong Lü, Shengnan Xia, Juncheng Li, Aayushi Mahajan, Shawn M. Davidson, Anna O. Basile, Caitlin P. McHugh, Jean Paul Vonsattel, Richard A. Hickman, Michael C. Zody, David E. Housman, James E. Goldman, Andrew S. Yoo, Vilas Menon, Osama Al‐Dalahmah

    Vydáno 2024
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  4. 4
    High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

    High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios Autor 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

    Vydáno 2022
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  5. 5
    Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation

    Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation Autor Jonas A. Gustafson, Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe, Lei Yang, Anthony A Snead, Phillip A. Richmond, Wouter De Coster, Nathan D. Olson, Andrea Guarracino, Qiuhui Li, Angela L Miller, Joy Goffena, Zachery Anderson, Sophie Storz, S. Ward, Maisha Sinha, Claudia Gonzaga‐Jauregui, Wayne E. Clarke, Anna O. Basile, André Corvelo, Catherine Reeves, Adrienne Helland, Rajeeva Musunuri, Mahler Revsine, Karynne Patterson, Cate Paschal, Christina Zakarian, Sara Goodwin, Tanner Jensen, E. Robb, W. Richard McCombie, Fritz J. Sedlazeck, Justin M. Zook, Stephen B. Montgomery, Erik Garrison, Mikhail Kolmogorov, Michael C. Schatz, Richard N. McLaughlin, Harriet Dashnow, Michael C. Zody, Matthew Loose, Miten Jain, Evan E. Eichler, Danny E. Miller

    Vydáno 2024
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  6. 6
    Haplotype-resolved diverse human genomes and integrated analysis of structural variation

    Haplotype-resolved diverse human genomes and integrated analysis of structural variation Autor 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

    Vydáno 2021
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  7. 7
    A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

    A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies Autor Yoonjung Yoonie Joo, Ky’Era V. Actkins, Jennifer A. Pacheco, Anna O. Basile, Robert J. Carroll, David R. Crosslin, Felix R. Day, Joshua C. Denny, Digna R. Velez Edwards, Hákon Hákonarson, John B. Harley, Scott J. Hebbring, Kevin Ho, Gail P. Jarvik, Michelle R. Jones, Tugce Karaderi, Frank Mentch, Cindy Meun, Bahram Namjou, Sarah A. Pendergrass, Marylyn D. Ritchie, Ian B. Stanaway, Margrit Urbanek, Theresa L. Walunas, Johanna L. Smith, Rex L. Chisholm, Abel Kho, Lea K. Davis, M. Geoffrey Hayes, Felix R. Day, Tugce Karaderi, Michelle R. Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Mägi, Richa Saxena, Triin Laisk-Podar, Margrit Urbanek, M. Geoffrey Hayes, Guðmar Þorleifsson, Juan Fernández‐Tajes, Anubha Mahajan, Benjamin H. Mullin, Bronwyn Stuckey, Timothy D. Spector, Scott G. Wilson, Mark O. Goodarzi, Lea K. Davis, Barbara Obermeyer-Pietsch, André G. Uitterlinden, Verneri Anttila, Benjamin M. Neale, Marjo‐Riitta Järvelin, Bart C.J.M. Fauser, Irina Kowalska, Jenny A. Visser, Marianne Anderson, Ken K. Ong, Elisabet Stener‐Victorin, David A. Ehrmann, Richard S. Legro, Andres Salumets, Mark I. McCarthy, Laure Morin‐Papunen, Unnur Þorsteinsdóttir, Hreinn Stefánsson, Unnur Styrkársdóttir, John R. B. Perry, Andrea Dunaif, Joop S.E. Laven, Steve Franks, Cecilia M. Lindgren, Corrine K. Welt

    Vydáno 2020
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