Search Results - Danny E. Miller
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Long live the king: chromosome-level assembly of the lion (Panthera leo) using linked-read, Hi-C, and long-read data by Ellie E. Armstrong, Ryan W. Taylor, Danny E. Miller, Christopher B. Kaelin, Gregory S. Barsh, Elizabeth A. Hadly, Dmitri A. Petrov
Published 2020Artigo -
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Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Gen... by Kandamurugu Manickam, Monica R. McClain, Laurie Demmer, Sawona Biswas, Hutton M. Kearney, Jennifer Malinowski, Lauren Massingham, Danny E. Miller, Timothy W. Yu, Fuki M. Hisama
Published 2021Artigo -
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Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast Meiosis by Xiangyu Chen, Ray T. Suhandynata, Rima Sandhu, Beth Rockmill, Neeman Mohibullah, Hengyao Niu, Jason Liang, Hsiao-Chi Lo, Danny E. Miller, Huilin Zhou, G. Valentin Börner, Nancy M. Hollingsworth
Published 2015Artigo -
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Corolla Is a Novel Protein That Contributes to the Architecture of the Synaptonemal Complex of <i>Drosophila</i> by Kimberly A. Collins, Jay R. Unruh, Brian D. Slaughter, Zulin Yu, Cathleen M. Lake, Rachel J. Nielsen, Kimberly S Box, Danny E. Miller, Justin P. Blumenstiel, Anoja Perera, Kathryn E Malanowski, R. Scott Hawley
Published 2014Artigo -
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A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development by Andrea Wilderman, Eva D’haene, Machteld Baetens, Tara N. Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E. Miller, Miranda Galey, Kari M. Brown, Rolf W. Stottmann, Sarah Vergult, K. Nicole Weaver, Samantha A. Brugmann, Timothy C. Cox, Justin Cotney
Published 2024Artigo -
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3-hour genome sequencing and targeted analysis to rapidly assess genetic risk by Miranda Pg Zalusky, Jonas A. Gustafson, Stephanie C. Bohaczuk, Benjamin J. Mallory, Paxton Reed, Tara Wenger, Erika Beckman, Irene J. Chang, Cate Paschal, Jillian G. Buchan, Christina M. Lockwood, Mihai Puia‐Dumitrescu, Daniel R. Garalde, Joseph Guillory, Androo J. Markham, Michael J. Bamshad, Evan E. Eichler, Andrew B. Stergachis, Danny E. Miller
Published 2024Artigo -
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SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns by Tara Wenger, Abbey Scott, Lukas Kruidenier, Megan Sikes, Alexandra Keefe, Kati J. Buckingham, Colby T. Marvin, Kathryn M. Shively, Tamara Bacus, Olivia Sommerland, Kailyn Anderson, Heidi Gildersleeve, Chayna Davis, Jamie Love‐Nichols, Katherine E. MacDuffie, Danny E. Miller, Joon‐Ho Yu, Amy Snook, Britt Johnson, David L. Veenstra, Julia Parish-Morris, Kirsty McWalter, Kyle Retterer, Deborah Copenheaver, Bethany Friedman, Jane Juusola, Erin Ryan, Renee Varga, Dan Doherty, Katrina M. Dipple, Jessica X. Chong, Paul Kruszka, Michael J. Bamshad
Published 2025Artigo -
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A complete reference genome improves analysis of human genetic variation by Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, Melanie Kirsche, Samantha Zarate, Pavel Avdeyev, Dylan J. Taylor, Kishwar Shafin, Alaina Shumate, Chunlin Xiao, Justin Wagner, Jennifer McDaniel, Nathan D. Olson, Michael Sauria, Mitchell R. Vollger, Arang Rhie, Melissa Meredith, Skylar Martin, Joyce Lee, Sergey Koren, Jeffrey Rosenfeld, Benedict Paten, Ryan M. Layer, Chen-Shan Chin, Fritz J. Sedlazeck, Nancy F. Hansen, Danny E. Miller, Adam M. Phillippy, Karen H. Miga, Rajiv C. McCoy, Megan Y. Dennis, Justin M. Zook, Michael C. Schatz
Published 2021Pré-impressão -
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A complete reference genome improves analysis of human genetic variation by Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, Melanie Kirsche, Samantha Zarate, Pavel Avdeyev, Dylan J. Taylor, Kishwar Shafin, Alaina Shumate, Chunlin Xiao, Justin Wagner, Jennifer McDaniel, Nathan D. Olson, Michael Sauria, Mitchell R. Vollger, Arang Rhie, Melissa Meredith, Skylar Martin, Joyce Lee, Sergey Koren, Jeffrey Rosenfeld, Benedict Paten, Ryan M. Layer, Chen-Shan Chin, Fritz J. Sedlazeck, Nancy F. Hansen, Danny E. Miller, Adam M. Phillippy, Karen H. Miga, Rajiv C. McCoy, Megan Y. Dennis, Justin M. Zook, Michael C. Schatz
Published 2022Artigo -
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Curated variation benchmarks for challenging medically relevant autosomal genes by Justin Wagner, Nathan D. Olson, Lindsay Harris, Jennifer McDaniel, Haoyu Cheng, Arkarachai Fungtammasan, Yih-Chii Hwang, Richa Gupta, Aaron M. Wenger, William J. Rowell, Ziad Khan, Jesse Farek, Yiming Zhu, Aishwarya Pisupati, Medhat Mahmoud, Chunlin Xiao, Byunggil Yoo, Sayed Mohammad Ebrahim Sahraeian, Danny E. Miller, David Jáspez, José M. Lorenzo-Salazar, Adrián Muñoz‐Barrera, Luis A. Rubio‐Rodríguez, Carlos Flores, Giuseppe Narzisi, Uday S. Evani, Wayne E. Clarke, Joyce Lee, Christopher E. Mason, Stephen E. Lincoln, Karen H. Miga, Mark Ebbert, Alaina Shumate, Heng Li, Chen-Shan Chin, Justin M. Zook, Fritz J. Sedlazeck
Published 2022Artigo -
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Highly contiguous assemblies of 101 drosophilid genomes by Bernard Kim, Jeremy Wang, Danny E. Miller, Olga Barmina, Emily Delaney, Ammon Thompson, Aaron A. Comeault, David Peede, Emmanuel R. R. D’Agostino, Julianne Peláez, Jessica M. Aguilar, Diler Haji, Teruyuki Matsunaga, Ellie E. Armstrong, Molly Zych, Yoshitaka Ogawa, Marina Stamenković‐Radak, Mihailo Jelić, Marija Savić Veselinović, Marija Tanasković, Pavle Erić, Jian‐Jun Gao, Takehiro K. Katoh, Masanori J. Toda, Hideaki Watabe, Masayoshi Watada, Jeremy S. Davis, Leonie C. Moyle, Giulia Manoli, Enrico Bertolini, Vladimı́r Košťál, R. Scott Hawley, Aya Takahashi, Corbin D. Jones, Donald K. Price, Noah K. Whiteman, Artyom Kopp, Daniel R. Matute, Dmitri A. Petrov
Published 2021Artigo -
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Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation by 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
Published 2024Pré-impressão -
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Targeted long-read sequencing identifies missing disease-causing variation by Danny E. Miller, Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson, Alexandra P. Lewis, Edith P. Almanza Fuerte, Catherine R. Paschal, Tom Walsh, Jenny Thies, James T. Bennett, Ian Glass, Katrina M. Dipple, Karynne Patterson, Emily Bonkowski, Zoe Nelson, Audrey Squire, Megan Sikes, Erika Beckman, Robin L. Bennett, Dawn Earl, Winston Lee, Rando Allikmets, Seth J. Perlman, Penny Chow, Anne Hing, Tara Wenger, Margaret P Adam, Angela Sun, Christina Lam, Irene J. Chang, Xue Zou, Stephanie Austin, Erin Huggins, Alexias Safi, Apoorva K. Iyengar, Timothy E. Reddy, William H. Majoros, Andrew S. Allen, Gregory E. Crawford, Priya S. Kishnani, Mary‐Claire King, Tim Cherry, Jessica X. Chong, Michael J. Bamshad, Deborah A. Nickerson, Heather C. Mefford, Dan Doherty, Evan E. Eichler
Published 2021Artigo
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