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

por Travers, Kevin J., Chin, Chen-Shan, Rank, David R., Eid, John S., Turner, Stephen W.
Publicado 2010

Sequencing the unsequenceable: Expanded CGG-repeat alleles of the fragile X gene

por Loomis, Erick W., Eid, John S., Peluso, Paul, Yin, Jun, Hickey, Luke, Rank, David, McCalmon, Sarah, Hagerman, Randi J., Tassone, Flora, Hagerman, Paul J.
Publicado 2013

Application of genomics to toxicology research.

por Thomas, Russell S, Rank, David R, Penn, Sharron G, Zastrow, Gina M, Hayes, Kevin R, Hu, Tianhua, Pande, Kalyan, Lewis, Mark, Jovanovich, Stevan B, Bradfield, Christopher A
Publicado 2002

Fully Phased Sequence of a Diploid Human Genome Determined de Novo from the DNA of a Single Individual

por Soifer, llya, Fong, Nicole L., Yi, Nelda, Ireland, Andrea T., Lam, Irene, Sooknah, Matthew, Paw, Jonathan S., Peluso, Paul, Concepcion, Gregory T., Rank, David, Hastie, Alex R., Jojic, Vladimir, Ruby, J. Graham, Botstein, David, Roy, Margaret A.
Publicado 2020

Highly accurate long-read HiFi sequencing data for five complex genomes

por Hon, Ting, Mars, Kristin, Young, Greg, Tsai, Yu-Chih, Karalius, Joseph W., Landolin, Jane M., Maurer, Nicholas, Kudrna, David, Hardigan, Michael A., Steiner, Cynthia C., Knapp, Steven J., Ware, Doreen, Shapiro, Beth, Peluso, Paul, Rank, David R.
Publicado 2020

Long-read, whole-genome shotgun sequence data for five model organisms

por Kim, Kristi E, Peluso, Paul, Babayan, Primo, Yeadon, P. Jane, Yu, Charles, Fisher, William W, Chin, Chen-Shan, Rapicavoli, Nicole A, Rank, David R, Li, Joachim, Catcheside, David E. A, Celniker, Susan E, Phillippy, Adam M, Bergman, Casey M, Landolin, Jane M
Publicado 2014

Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution

por Melters, Daniël P, Bradnam, Keith R, Young, Hugh A, Telis, Natalie, May, Michael R, Ruby, J Graham, Sebra, Robert, Peluso, Paul, Eid, John, Rank, David, Garcia, José Fernando, DeRisi, Joseph L, Smith, Timothy, Tobias, Christian, Ross-Ibarra, Jeffrey, Korf, Ian, Chan, Simon WL
Publicado 2013

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

por Wenger, Aaron M., Peluso, Paul, Rowell, William J., Chang, Pi-Chuan, Hall, Richard J., Concepcion, Gregory T., Ebler, Jana, Fungtammasan, Arkarachai, Kolesnikov, Alexey, Olson, Nathan D., Töpfer, Armin, Alonge, Michael, Mahmoud, Medhat, Qian, Yufeng, Chin, Chen-Shan, Phillippy, Adam M., Schatz, Michael C., Myers, Gene, DePristo, Mark A., Ruan, Jue, Marschall, Tobias, Sedlazeck, Fritz J., Zook, Justin M., Li, Heng, Koren, Sergey, Carroll, Andrew, Rank, David R., Hunkapiller, Michael W.
Publicado 2019

Improved maize reference genome with single-molecule technologies

por Jiao, Yinping, Peluso, Paul, Shi, Jinghua, Liang, Tiffany, Stitzer, Michelle C., Wang, Bo, Campbell, Michael S., Stein, Joshua C., Wei, Xuehong, Chin, Chen-Shan, Guill, Katherine, Regulski, Michael, Kumari, Sunita, Olson, Andrew, Gent, Jonathan, Schneider, Kevin L., Wolfgruber, Thomas K., May, Michael R., Springer, Nathan M., Antoniou, Eric, McCombie, W. Richard, Presting, Gernot G., McMullen, Michael, Ross-Ibarra, Jeffrey, Dawe, R. Kelly, Hastie, Alex, Rank, David R., Ware, Doreen
Publicado 2017