Resultados de procura - Danny E. Miller

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  1. 1
    Applications of long-read sequencing to Mendelian genetics

    Applications of long-read sequencing to Mendelian genetics por Francesco Mastrorosa, Danny E. Miller, Evan E. Eichler

    Publicado 2023
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  2. 2
    Highly Contiguous Genome Assemblies of 15 <i>Drosophila</i> Species Generated Using Nanopore Sequencing

    Highly Contiguous Genome Assemblies of 15 <i>Drosophila</i> Species Generated Using Nanopore Sequencing por Danny E. Miller, Cynthia Staber, Julia Zeitlinger, R. Scott Hawley

    Publicado 2018
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  3. 3
    Local Inversion Heterozygosity Alters Recombination throughout the Genome

    Local Inversion Heterozygosity Alters Recombination throughout the Genome por K. Nicole Crown, Danny E. Miller, Jeff Sekelsky, R. Scott Hawley

    Publicado 2018
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  4. 4
    Female Meiosis: Synapsis, Recombination, and Segregation in <i>Drosophila melanogaster</i>

    Female Meiosis: Synapsis, Recombination, and Segregation in <i>Drosophila melanogaster</i> por Stacie E. Hughes, Danny E. Miller, Angela L Miller, R. Scott Hawley

    Publicado 2018
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  5. 5
    Advances in the discovery and analyses of human tandem repeats

    Advances in the discovery and analyses of human tandem repeats por Mark Chaisson, Arvis Sulovari, Paul N. Valdmanis, Danny E. Miller, Evan E. Eichler

    Publicado 2023
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  6. 6
    Rapid Low-Cost Assembly of the <i>Drosophila melanogaster</i> Reference Genome Using Low-Coverage, Long-Read Sequencing

    Rapid Low-Cost Assembly of the <i>Drosophila melanogaster</i> Reference Genome Using Low-Coverage, Long-Read Sequencing por Edwin Solares, Mahul Chakraborty, Danny E. Miller, Shannon Kalsow, Kate Hall, Anoja Perera, J. J. Emerson, R. Scott Hawley

    Publicado 2018
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  7. 7
    Long live the king: chromosome-level assembly of the lion (Panthera leo) using linked-read, Hi-C, and long-read data

    Long live the king: chromosome-level assembly of the lion (Panthera leo) using linked-read, Hi-C, and long-read data por Ellie E. Armstrong, Ryan W. Taylor, Danny E. Miller, Christopher B. Kaelin, Gregory S. Barsh, Elizabeth A. Hadly, Dmitri A. Petrov

    Publicado 2020
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  8. 8
    Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes

    Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes por Cate Paschal, Miranda Galey, Anita Beck, Madelyn A. Gillentine, Jaya Narayanan, Nikhita Damaraju, Joy Goffena, Sophie Storz, Danny E. Miller

    Publicado 2025
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  9. 9
    Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

    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... por 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

    Publicado 2021
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  10. 10
    Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast Meiosis

    Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast Meiosis por 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

    Publicado 2015
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  11. 11
    Corolla Is a Novel Protein That Contributes to the Architecture of the Synaptonemal Complex of <i>Drosophila</i>

    Corolla Is a Novel Protein That Contributes to the Architecture of the Synaptonemal Complex of <i>Drosophila</i> por 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

    Publicado 2014
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  12. 12
    A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

    A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development por 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

    Publicado 2024
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  13. 13
    3-hour genome sequencing and targeted analysis to rapidly assess genetic risk

    3-hour genome sequencing and targeted analysis to rapidly assess genetic risk por 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

    Publicado 2024
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  14. 14
    SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns

    SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns por 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

    Publicado 2025
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  15. 15
    A complete reference genome improves analysis of human genetic variation

    A complete reference genome improves analysis of human genetic variation por 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

    Publicado 2021
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  16. 16
    A complete reference genome improves analysis of human genetic variation

    A complete reference genome improves analysis of human genetic variation por 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

    Publicado 2022
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  17. 17
    Curated variation benchmarks for challenging medically relevant autosomal genes

    Curated variation benchmarks for challenging medically relevant autosomal genes por 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

    Publicado 2022
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  18. 18
    Highly contiguous assemblies of 101 drosophilid genomes

    Highly contiguous assemblies of 101 drosophilid genomes por 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

    Publicado 2021
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  19. 19
    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 por 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

    Publicado 2024
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  20. 20
    Targeted long-read sequencing identifies missing disease-causing variation

    Targeted long-read sequencing identifies missing disease-causing variation por 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

    Publicado 2021
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