Resultats de la cerca - David R. Rank

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  1. 1
    A flexible and efficient template format for circular consensus sequencing and SNP detection

    A flexible and efficient template format for circular consensus sequencing and SNP detection per Kevin Travers, Chen-Shan Chin, David R. Rank, John Eid, Steve Turner

    Publicat 2010
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  2. 2
    Sequencing the unsequenceable: Expanded CGG-repeat alleles of the fragile X gene

    Sequencing the unsequenceable: Expanded CGG-repeat alleles of the fragile X gene per Erick Loomis, John Eid, Paul Peluso, Jun Yin, Luke Hickey, David R. Rank, Sarah A. McCalmon, Randi J. Hagerman, Flora Tassone, Paul J. Hagerman

    Publicat 2012
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  3. 3
    A draft phased assembly of the diploid Cascade hop (<i>Humulus lupulus</i>) genome

    A draft phased assembly of the diploid Cascade hop (<i>Humulus lupulus</i>) genome per Lillian K. Padgitt‐Cobb, Sarah B. Kingan, Jackson Wells, Justin Elser, Brent A. Kronmiller, Daniel Moore, Gregory T. Concepcion, Paul Peluso, David R. Rank, Pankaj Jaiswal, John A. Henning, David A. Hendrix

    Publicat 2021
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  4. 4
    Highly accurate long-read HiFi sequencing data for five complex genomes

    Highly accurate long-read HiFi sequencing data for five complex genomes per Ting Hon, Kristin Mars, Greg Young, Yu‐Chih Tsai, Joseph W. Karalius, Jane M. Landolin, Nicholas Maurer, David Kudrna, Michael A. Hardigan, Cynthia Steiner, Steven J. Knapp, Doreen Ware, Beth Shapiro, Paul Peluso, David R. Rank

    Publicat 2020
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  5. 5
    Long-read, whole-genome shotgun sequence data for five model organisms

    Long-read, whole-genome shotgun sequence data for five model organisms per Kristi E. Kim, Paul Peluso, Primo Babayan, P. Jane Yeadon, Charles Yu, William W. Fisher, Chen-Shan Chin, Nicole A. Rapicavoli, David R. Rank, Joaquim Li, David Catcheside, S Celniker, Adam M. Phillippy, Casey Bergman, Jane M. Landolin

    Publicat 2014
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  6. 6
    Highly-accurate long-read sequencing improves variant detection and assembly of a human genome

    Highly-accurate long-read sequencing improves variant detection and assembly of a human genome per Aaron M. Wenger, Paul Peluso, William J. Rowell, Pi-Chuan Chang, Richard Hall, Gregory T. Concepcion, Jana Ebler, Arkarachai Fungtammasan, Alexey Kolesnikov, Nathan D. Olson, Armin Töpfer, Michael Alonge, Medhat Mahmoud, Y. Qian, Chen-Shan Chin, Adam M. Phillippy, Michael C. Schatz, Gene Myers, Mark A. DePristo, Jue Ruan, Tobias Marschall, Fritz J. Sedlazeck, Justin M. Zook, Heng Li, Sergey Koren, Andrew Carroll, David R. Rank, Michael W. Hunkapiller

    Publicat 2019
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  7. 7
    Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

    Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome per Aaron M. Wenger, Paul Peluso, William J. Rowell, Pi-Chuan Chang, Richard Hall, Gregory T. Concepcion, Jana Ebler, Arkarachai Fungtammasan, Alexey Kolesnikov, Nathan D. Olson, Armin Töpfer, Michael Alonge, Medhat Mahmoud, Yufeng Qian, Chen-Shan Chin, Adam M. Phillippy, Michael C. Schatz, Gene Myers, Mark A. DePristo, Jue Ruan, Tobias Marschall, Fritz J. Sedlazeck, Justin M. Zook, Heng Li, Sergey Koren, Andrew Carroll, David R. Rank, Michael W. Hunkapiller

    Publicat 2019
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  8. 8
    Origins of the<i>E. coli</i>Strain Causing an Outbreak of Hemolytic–Uremic Syndrome in Germany

    Origins of the<i>E. coli</i>Strain Causing an Outbreak of Hemolytic–Uremic Syndrome in Germany per David A. Rasko, Dale R. Webster, Jason W. Sahl, Ali Bashir, Nadia Boisen, Flemming Scheutz, Ellen E. Paxinos, Robert Sebra, Chen-Shan Chin, D Iliopoulos, Aaron A. Klammer, Paul Peluso, Lawrence Lee, Andrey Kislyuk, James W. Bullard, Andrew Kasarskis, Susanna Wang, John Eid, David R. Rank, Julia C. Redman, Susan R. Steyert, Jakob Frimodt-Møller, Carsten Struve, Andreas Munk Petersen, Karen A. Krogfelt, James P. Nataro, Eric E. Schadt, Matthew K. Waldor

    Publicat 2011
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  9. 9
    Improved maize reference genome with single-molecule technologies

    Improved maize reference genome with single-molecule technologies per Yinping Jiao, Paul Peluso, Jinghua Shi, Tiffany Y Liang, Michelle C. Stitzer, Bo Wang, Michael S. Campbell, Joshua C. Stein, Xuehong Wei, Chen-Shan Chin, Katherine E. Guill, Michael Regulski, Sunita Kumari, Andrew Olson, Jonathan I. Gent, Kevin Schneider, Thomas Wolfgruber, Michael R. May, Nathan M. Springer, Eric Antoniou, W. Richard McCombie, Gernot G. Presting, Michael D. McMullen, Jeffrey Ross‐Ibarra, R. Kelly Dawe, Alex Hastie, David R. Rank, Doreen Ware

    Publicat 2017
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