Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Raymond D. Miller"'
Publikováno v:
BioTechniques, Vol 32, Iss 6S, Pp S28-S32 (2002)
To achieve high-throughput analysis of allele frequencies in human SNPs, we have developed automated methods for designing PCR and DNA sequencing primers. We found we could run the PCR assays at quite stringent, uniform conditions. The design process
Externí odkaz:
https://doaj.org/article/4268aff000ed498eb115beebdb6af93c
Autor:
Joseph A Ross, Daniel C Koboldt, Julia E Staisch, Helen M Chamberlin, Bhagwati P Gupta, Raymond D Miller, Scott E Baird, Eric S Haag
Publikováno v:
PLoS Genetics, Vol 7, Iss 7, p e1002174 (2011)
The nematode Caenorhabditis briggsae is an emerging model organism that allows evolutionary comparisons with C. elegans and exploration of its own unique biological attributes. To produce a high-resolution C. briggsae recombination map, recombinant i
Externí odkaz:
https://doaj.org/article/1205429703fa4fcd94c534a1127e592d
Autor:
LaDeana W Hillier, Raymond D Miller, Scott E Baird, Asif Chinwalla, Lucinda A Fulton, Daniel C Koboldt, Robert H Waterston
Publikováno v:
PLoS Biology, Vol 5, Iss 7, p e167 (2007)
To determine whether the distinctive features of Caenorhabditis elegans chromosomal organization are shared with the C. briggsae genome, we constructed a single nucleotide polymorphism-based genetic map to order and orient the whole genome shotgun as
Externí odkaz:
https://doaj.org/article/4a9fc8e6c0b94e84b49bd469afed13f4
Autor:
Jessica Watkin, Stacey Gabriel, Norio Niikawa, Michael Boehnke, Lincoln Stein, Karen Kennedy, Mark Leppert, Renzong Qiu, John Stewart, Peter E. Chen, Panos Deloukas, Wei Huang, Deborah A. Nickerson, Fuli Yu, Sarah E. Hunt, Ming Xiao, Francis S. Collins, Fiona Cunningham, Stephen F. Schaffner, Yoshimitsu Fukushima, Jonathan Marchini, Troy Duster, Jane Peterson, Koki Sorimachi, Michael Feolo, Bruce S. Weir, Paul L'Archevêque, Raymond D. Miller, Hongguang Wang, Toyin Aniagwu, Mildred K. Cho, Darryl Macer, Qingrun Zhang, Paul K.H. Tam, Ardavan Kanani, Guy Bellemare, Thomas D. Willis, Mark Shillito, Martin Leboeuf, Lynn F. Zacharia, Pilar N. Ossorio, Charmaine D.M. Royal, Paul Hardenbol, Yusuke Nakamura, Maria Jasperse, Pui-Yan Kwok, Mark S. Guyer, Bin Liu, Leonid Kruglyak, Huanming Yang, Aravinda Chakravarti, John W. Belmont, Ellen Wright Clayton, Jane Rogers, Arnold Oliphant, Jack Spiegel, Houcan Zhang, Stephen T. Sherry, Vincent Ferretti, Julio Licinio, Toshihiro Tanaka, Richard R. Hudson, Mary M.Y. Waye, Lon R. Cardon, Elke Jordan, Gonçalo R. Abecasis, Kazuto Kato, Vivian Ota Wang, Gilean McVean, Lawrence M. Sung, Don Powell, Patricia A. Marshall, Patricia Spallone, Lan Yang Ch'Ang, Alastair Kent, James C. Mullikin, Eric S. Lander, Lucinda Fulton, Michael S. Phillips, Jeffrey Tze Fei Wong, David Valle, Fanny Chagnon, Semyon Kruglyak, Tatsuhiko Tsunoda, Hua Han, John P. Rice, David J. Cutler, Mark J. Daly, Peter Donnelly, Yan Shen, Jean E. McEwen, Andrew P. Morris, Richard Seabrook, Luana Galver, Thomas J. Hudson, Chibuzor Nkwodimmah, Clement Adebamowo, Lisa D. Brooks, Arthur L. Holden, Robert L. Nussbaum, David R. Bentley, Jeffrey C. Long, Nancy L. Saccone, Michael Dunn, Charles N. Rotimi, Sarah S. Murray, Richard A. Gibbs, Simon Myers, George M. Weinstock, Bartha Maria Knoppers, Takashi Fujita, Julie A. Douglas, Georgia M. Dunston, Richard K. Wilson, Sharon F. Terry, Kazuo Todani, Akihiro Sekine, Barbara Skene, Martin Godbout, David Altshuler, Bruce W. Birren, Lynn B. Jorde, Mark S. Chee, Olayemi Matthew, Erica Sodergren, Lap-Chee Tsui, Changqing Zeng, John C. Wallenburg, Missy Dixon, Gudmundur A. Thorisson, Ichiro Matsuda, Andrei Verner, Carl S. Kashuk, Eiji Yoshino, Patricia Taillon-Miller, Morris W. Foster, Satoshi Tanaka, Alexandre Montpetit, Yoichi Tanaka, Denise L. Lind, Eric H. Lai, Eiko Suda, Shenghui Duan
The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b68509775c60ce3a8e33fadcb656b72
https://ora.ox.ac.uk/objects/uuid:64fb68cf-6299-4b37-9248-e41084f26570
https://ora.ox.ac.uk/objects/uuid:64fb68cf-6299-4b37-9248-e41084f26570
Autor:
Raymond D. Miller, Daniel C. Koboldt
Publikováno v:
Genomics: Essential Methods
Autor:
Ryan Christensen, Michael Elashoff, Robert B. Belshe, Patricia Taillon-Miller, Daniel C. Koboldt, Nancy L. Saccone, Jianhua Guo, Samuel L. Stanley, Sharon E. Frey, Raymond D. Miller
Publikováno v:
The Journal of Infectious Diseases. 196:212-219
We hypothesized that individuals who develop fever after smallpox vaccination have genetically determined differences in their immune responses to vaccinia virus. We looked for an association between the development of fever and single-nucleotide pol
Publikováno v:
Human Mutation. 27:249-254
Utilizing the results of extensive single nucleotide polymorphism (SNP) studies in humans, stimulated by the International HapMap Project, we present evidence that SNPs are not randomly spaced across the genome, but are somewhat clustered. This obser
Autor:
Marko Babjuk, Timothy Barder, Douglas M. Potter, Raymond D. Miller, Thu-Suong Van Le, Robert H. Getzenberg
Publikováno v:
Urology. 66:1256-1260
Available online 16 December 2005 This article has been retracted: please see Elsevier Policy on Article Withdrawal ( http://www.elsevier.com/locate/withdrawalpolicy ). This article has been retracted at the request of the Authors. Two potential issu
Autor:
Mark Leppert, Aravinda Chakravarti, Charmaine D.M. Royal, Sarah S. Murray, Renzong Qiu, Panos Deloukas, Renwu Wang, David A. Hinds, Barbara E. Stranger, Xiaoli Tang, Huanming Yang, John W. Belmont, Nigel P. Carter, Huy Nguyen, William Mak, Kazuto Kato, Shiran Pasternak, Chaohua Li, Jeffrey C. Barrett, Lon R. Cardon, Vincent Ferretti, Atsushi Nagashima, Peter E. Chen, Stephen F. Schaffner, Hongbo Fu, Zhu Chen, Siqi Liu, John Burton, Paul Hardenbol, Gudmundur A. Thorisson, Yusuke Nakamura, Mark Griffiths, Imtiaz Yakub, Eiko Suda, Gonçalo R. Abecasis, Carl S. Kashuk, Qingrun Zhang, Yoshimitsu Fukushima, Karen Kennedy, Sarah E. Hunt, Yi Wang, Norio Niikawa, Ichiro Matsuda, Lynn F. Zacharia, Lalitha Krishnan, Zhen Wang, Stéphanie Roumy, C M Clee, David J. Cutler, Albert V. Smith, Lincoln Stein, Simon Myers, Jane Peterson, Jun Zhou, Yozo Ohnishi, Weihua Guan, Matthew Stephens, Xiaoyan Xiong, Julian Maller, Houcan Zhang, Pui-Yan Kwok, Mark S. Guyer, Liuda Ziaugra, Jonathan Witonsky, Matthew C. Jones, Stacey Gabriel, You-Qiang Song, Daochang An, Haifeng Wang, Gilean McVean, Lawrence M. Sung, Zhijian Yao, Yan Shen, Yangfan Liu, George M. Weinstock, Ludmila Pawlikowska, Erica Sodergren, Mark T. Ross, Andrew Boudreau, Toshihiro Tanaka, Thomas D. Willis, Weitao Hu, Kelly A. Frazer, Li Jin, Robert W. Plumb, Paul I.W. de Bakker, Hongbin Zhao, Wei Lin, Sarah Sims, Richard A. Gibbs, Maura Faggart, Michael Feolo, Dennis G. Ballinger, Xun Chu, Lucinda Fulton, Marcos Delgado, Ellen Winchester, Wei Huang, Fuli Yu, Christianne R. Bird, Shaun Purcell, Jessica Roy, Dongmei Cai, Launa M. Galver, Bartha Maria Knoppers, Emmanouil T. Dermitzakis, Gao Yang, Takashi Morizono, Rachel Barry, Kirsten McLay, Daryl J. Thomas, Steve McCarroll, Jonathan Marchini, Daniel J. Richter, Andy Peiffer, Patricia Taillon-Miller, Richard K. Wilson, Stephen Kwok-Wing Tsui, Jian-Bing Fan, Lisa D. Brooks, Laura L. Stuve, Paul L'Archevêque, David M. Evans, Clémentine Sallée, Peter Donnelly, Hong Xue, Hui Zhao, Charles N. Rotimi, Jean E. McEwen, J. Tze Fei Wong, Hao Pan, Alastair Kent, Brendan Blumenstiel, Qing Li, Weiwei Sun, L. Kang, Colin Freeman, John Stewart, Chibuzor Nkwodimmah, Morris W. Foster, Don Powell, Leonardo Bottolo, Raymond D. Miller, Stephen T. Sherry, Francis S. Collins, Donna M. Muzny, Jun Yu, Ike Ajayi, Hua Han, Pardis C. Sabeti, Hongguang Wang, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Guy Bellemare, Zhaohui S. Qin, H. B. Hu, Jane Rogers, Thomas J. Hudson, Mark J. Daly, Andrew P. Morris, Supriya Gupta, Ming Xiao, Patrick Varilly, Nick Patterson, Akihiro Sekine, Chris C. A. Spencer, Jonathan Morrison, Missy Dixon, Paul K.H. Tam, Jian Wang, Matthew Defelice, Susana Eyheramendy, Michael Shi, Yungang He, Ellen Wright Clayton, Richa Saxena, Heather M. Munro, Arthur L. Holden, Yayun Shen, Christine P. Bird, Bruce W. Birren, Itsik Pe'er, David R. Bentley, Lynne V. Nazareth, Pamela Whittaker, Pak C. Sham, Amy L. Camargo, David A. Wheeler, Koji Saeki, Martin Godbout, David Altshuler, Liang Xu, Ying Wang, David Willey, Alexandre Montpetit, Shin Lin, Michael S. Phillips, Changqing Zeng, Clement Adebamowo, John C. Wallenburg, Mark S. Chee, Ben Fry, Erich Stahl, Melissa Parkin, Rhian Gwilliam, Andrei Verner, Patrick J. Nailer, Lap-Chee Tsui, Bo Zhang, Fanny Chagnon, David R. Cox, Jack Spiegel, Jamie Moore, Vivian Ota Wang, Patricia A. Marshall, Takuya Kitamoto, Bruce S. Weir, Darryl Macer, Geraldine M. Clarke, Robert C. Onofrio, Mary M.Y. Waye, Wei Wang, Suzanne M. Leal, James C. Mullikin, Toyin Aniagwu, Daniel C. Koboldt, Mary Goyette, Martin Leboeuf, Isaac F. Adewole, Ruth Jamieson, Arnold Oliphant, Jessica Watkin, Jean François Olivier
Publikováno v:
Europe PubMed Central
Inherited genetic variation has a critical but as yet largely uncharacterized role in human disease. Here we report a public database of common variation in the human genome: more than one million single nucleotide polymorphisms (SNPs) for which accu
Autor:
Elizabeth G. Lovins, Gira J Shah, J Rebecca White, David W Morris, M. A. Donaldson, Michael A Mockler, Chad E Callahan, Sangmee Ahn Jo, Sima Maggan, Shobha Varde, Yeon-Kyeong Yoo, Stacey E Ford, Benjamin J Carey, Chan Park, Angela M Forman, Sung Chul Jung, Andrew J Reinhart, Maria L Lundy, Nicholas Addleman, Pui-Yan Kwok, Ravi Sachidanandam, Sun Mi In, Stephanie L Restine, Craig A. Gelfand, Nicholas Pavelka, Jennifer M Kuebler, Carolina Elosua, Cheryl L Conley, Hamid A Bhatti, Inho Jo, Michael S. Phillips, Vram Derohannessian, Stephanie A Livingston, Daniel C. Koboldt, Ellen F. Kloss, Kuchan Kimm, Rachel A Donaldson, Jong-Keuk Lee, Amy Walters, Adrienne B Perkins, J. F. Studebaker, Fengshen Kuo, Diana L Jackson, Nicole M Grecco, Mark J Hozza, Bermseok Oh, Eric P Nachtman, Kathryn E Scott, Jessica A Lathrop, Michael T Boyce-Jacino, Susan M Gutendorf, Wendy Ankener, Sook Kim, Matthew R Minton, Kathy L Leis, Jong Eun Lee, Cricket R Hock, Chang-Wook Park, Soyoung Hur, Justin M Cyr, Jatana M Tate, Steven V Alfisi, Raymond D. Miller
Publikováno v:
Genomics. 86:117-126
Here we report a large, extensively characterized set of single-nucleotide polymorphisms (SNPs) covering the human genome. We determined the allele frequencies of 55,018 SNPs in African Americans, Asians (Japanese-Chinese), and European Americans as