Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Brad Sickler"'
Autor:
Rob Knight, David T.W. Wong, Peter De Hoff, Phillip G. Febbo, Kelly M. Schiabor Barrett, Jimmy M. Ramirez, Alexandre Bolze, Eric McDonald, Louise C. Laurent, Ezra Kurzban, David M. Becker, Michael Worobey, Emily Spencer, Marc Laurent, Duncan MacCannell, Kimberly Gietzen, Venice Servellita, Aaron Harding, Catelyn Anderson, Phoebe Seaver, Marc A. Suchard, Magnus Isaksson, Shashank Sathe, Brett Austin, Tracy Basler, Candace Wang, Holly Valentine, Simon R. White, Jason Nguyen, Sharoni Jacobs, Charles Y. Chiu, Laura D. Hughes, Mark Zeller, James T. Lu, Karthik Gangavarapu, Refugio Robles-Sikisaka, Kristian G. Andersen, Charlotte Rivera-Garcia, Kelly Hoon, Brad Sickler, Gene W. Yeo, Brendan B. Larsen, Nicole L. Washington, Eileen de Feo, Xueqing Wang, Jingtao Liu, Efren Sandoval, Omid Bakhtar, Jay Antico, Elizabeth T. Cirulli, Geraint Levan, William E. Lee, Tyler Cassens, Xianding Deng
Publikováno v:
Cell, vol 184, iss 10
Cell
Cell
The highly transmissible B.1.1.7 variant of SARS-CoV-2, first identified in the United Kingdom, has gained a foothold across the world. Using S gene target failure (SGTF) and SARS-CoV-2 genomic sequencing, we investigated the prevalence and dynamics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6156b6175639d01493ddbb60f74960c
https://escholarship.org/uc/item/2rw0t09q
https://escholarship.org/uc/item/2rw0t09q
Autor:
Omid Bakhtar, Jay Antico, Brendan B. Larsen, Catelyn Anderson, Louise C. Laurent, Brett Austin, Nicole L. Washington, Simon R. White, Kelly M. Schiabor Barrett, Geraint Levan, Kristian G. Andersen, Eileen de Feo, Phoebe Seaver, Magnus Isaksson, Xianding Deng, Sharoni Jacobs, William E. Lee, Ezra Kurzban, Peter De Hoff, Candace Wang, Emily Spencer, Venice Servellita, Phil Febbo, Michael Worobey, Shashank Sathe, Kelly Hoon, Brad Sickler, David T.W. Wong, Jimmy M. Ramirez, Gene W. Yeo, Karthik Gangavarapu, Kimberly Gietzen, Jingtao Liu, Xueqing Wang, Efren Sandoval, Aaron Harding, Holly Valentine, Eric McDonald, Marc A. Suchard, Mark Zeller, Charlotte Rivera-Garcia, Charles Y. Chiu, Elizabeth T. Cirulli, David M. Becker, Marc Laurent, James T. Lu, Refugio Robles-Sikisaka, Jason Nguyen, Tracy Basler, Rob Knight, Alexandre Bolze, Tyler Cassens, Laura D. Hughes
Publikováno v:
medRxiv
medRxiv, vol 2, iss 02-09
medRxiv, vol 2, iss 02-09
Author(s): Washington, Nicole L; Gangavarapu, Karthik; Zeller, Mark; Bolze, Alexandre; Cirulli, Elizabeth T; Schiabor Barrett, Kelly M; Larsen, Brendan B; Anderson, Catelyn; White, Simon; Cassens, Tyler; Jacobs, Sharoni; Levan, Geraint; Nguyen, Jason
Autor:
Ripan S Malhi, Brad Sickler, Dawei Lin, Jessica Satkoski, Raul Y Tito, Debbie George, Sreetharan Kanthaswamy, David Glenn Smith
Publikováno v:
PLoS ONE, Vol 2, Iss 5, p e438 (2007)
We developed a novel method for identifying SNPs widely distributed throughout the coding and non-coding regions of a genome. The method uses large-scale parallel pyrosequencing technology in combination with bioinformatics tools. We used this method
Externí odkaz:
https://doaj.org/article/3c2e07e5b34a4c828d78832bc0ef16fd
Autor:
Brad Sickler
The human brain is incredibly complex. Both Christian and secular scholars alike affirm this fact, yet the traditional view of humanity as spiritual beings made in the image of God has come under increased pressure from humanistic and materialistic t
Autor:
Eric J. Small, Lawrence Fong, Karen E. Knudsen, Brad Sickler, Robert E. Reiter, Charles J. Ryan, Theodore C. Goldstein, Tomasz M. Beer, Martin E. Gleave, Rahul Aggarwal, Julian S. Gehring, Rajdeep Das, John Shon, Scott M. Dehm, Alan Ashworth, David A. Quigley, Ha X. Dang, Terence W. Friedlander, R. Keira Cheetham, Denise Playdle, Paul Lloyd, Serafim Batzoglou, Jack F. Youngren, Jin Zhang, Nathan A. Lack, Adam Foye, Felix Y. Feng, Jörg Hakenberg, Adina M. Bailey, Owen N. Witte, Abhijit Parolia, Scott A. Tomlins, Travis J. Barnard, Donavan T. Cheng, Jiaoti Huang, Li Zhang, P. G. Febbo, Alexander W. Wyatt, Kim N. Chi, Matthew Rettig, Vishal Kothari, Daniel E. Spratt, Housheng Hansen He, Haolong Li, George Thomas, Arnold Liao, Shuang G. Zhao, Hui Li, Joshua M. Stuart, Won Kim, Primo N. Lara, Christopher G. Maher, Jonathan Chou, Joshi J. Alumkal, Amina Zoubeidi, Marc D. Perry, Ruhollah Moussavi-Baygi, Luke A. Gilbert, Arul M. Chinnaiyan, Christopher P. Evans, Hani Goodarzi, Marcin Cieslik, Kyle Kai-How Farh
Publikováno v:
Cell, vol 174, iss 3
Quigley, DA; Dang, HX; Zhao, SG; Lloyd, P; Aggarwal, R; Alumkal, JJ; et al.(2018). Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer. Cell, 174(3), 758-769.e9. doi: 10.1016/j.cell.2018.06.039. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/796124qb
Quigley, DA; Dang, HX; Zhao, SG; Lloyd, P; Aggarwal, R; Alumkal, JJ; et al.(2018). Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer. Cell, 174(3), 758-769.e9. doi: 10.1016/j.cell.2018.06.039. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/796124qb
© 2018 Elsevier Inc. While mutations affecting protein-coding regions have been examined across many cancers, structural variants at the genome-wide level are still poorly defined. Through integrative deep whole-genome and -transcriptome analysis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1928a409b1341bcafb393804416865b5
https://escholarship.org/uc/item/796124qb
https://escholarship.org/uc/item/796124qb
Autor:
Jodi A. Scheffler, Earl Taliercio, Candace H. Haigler, Jonathan F. Wendel, Andrew H. Paterson, Karl Haller, Yeisoo Yu, Jin Ying Guo, Jinfeng Suo, Margaret L. Pierce, Randell Allen, Curtis G. Wilkerson, Michael E. Sparks, Ricky Turley, Jamie Hatfield, Natalya Klueva, Xiao-Ya Chen, Stefan R. Schulze, Aladdin B. Arpat, Deshui Zhang, Hyeran Kim, Rod A. Wing, Jordan M. Swanson, Margaret Essenberg, David Kudrna, Danny J. Llewellyn, Helen G. McFadden, Thea A. Wilkins, Joshua A. Udall, Caitriona Dowd, Elizabeth S. Dennis, Yingru Wu, Cari Soderlund, Brad Sickler, Ryan A. Rapp, Paxton Payton
Publikováno v:
Genome Research. 16:441-450
Approximately 185,000GossypiumEST sequences comprising >94,800,000 nucleotides were amassed from 30 cDNA libraries constructed from a variety of tissues and organs under a range of conditions, including drought stress and pathogen challenges. These l
Autor:
Julianno B. M. Sambatti, Brad Sickler
Publikováno v:
Molecular Ecology Notes. 6:594-596
We have developed two pieces of Perl and Python codes to calculate the natural log of lambda, a quantity that expresses deviations from Hardy–Weinberg equilibrium, and R, a weighted correlation coefficient between alleles of locus pairs as a quanti
Publikováno v:
Modern Clinical Molecular Techniques ISBN: 9781461421696
With the advent of massively parallel sequencing (MPS) technologies, it is now possible to sequence an entire human genome for about the price it would cost to sequence four or five genes at comparable accuracy using Sanger sequencing methods. In thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b9be223ae76bb29a7120abe797104ec
https://doi.org/10.1007/978-1-4614-2170-2_5
https://doi.org/10.1007/978-1-4614-2170-2_5
Autor:
Dawei Lin, Jessica Satkoski, David Glenn Smith, Ripan S. Malhi, Sreetharan Kanthaswamy, Debbie George, Brad Sickler, Raul Y. Tito
Publikováno v:
PLoS ONE
PLoS ONE, Vol 2, Iss 5, p e438 (2007)
PLoS ONE, Vol 2, Iss 5, p e438 (2007)
We developed a novel method for identifying SNPs widely distributed throughout the coding and non-coding regions of a genome. The method uses large-scale parallel pyrosequencing technology in combination with bioinformatics tools. We used this method
Autor:
Russell J. Kohel, Young-Hoon Park, David M. Stelly, Roy G. Cantrell, O. M. El-Shihy, Brad Sickler, Magdy S. Alabady, Thea A. Wilkins, John Z. Yu, Mauricio Ulloa
Publikováno v:
Molecular genetics and genomics : MGG. 274(4)
There is an immediate need for a high-density genetic map of cotton anchored with fiber genes to facilitate marker-assisted selection (MAS) for improved fiber traits. With this goal in mind, genetic mapping with a new set of microsatellite markers [c