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The Sequence of the Human Genome [PDF]
Science, 2001 A 2.91-billion base pair (bp) consensus sequence of the euchromatic portion of the human genome was generated by the whole-genome shotgun sequencing method. The 14.8-billion bp DNA sequence was generated over 9 months from 27,271,853 high-quality sequence reads (5.11-fold coverage of the genome) from both ends of plasmid clones made from the DNA of ...J. Venter, M. Adams, E. Myers, Peter W. Li, R. Mural, G. Sutton, Hamilton O. Smith, M. Yandell, C. Evans, R. Holt, J. Gocayne, P. Amanatides, R. Ballew, D. Huson, J. Wortman, Qing Zhang, C. Kodira, Xiangqun H. Zheng, Lin Chen, M. Skupski, G. Subramanian, P. Thomas, Jinghui Zhang, George L. Gabor Miklos, C. Nelson, S. Broder, A. Clark, Joe Nadeau, V. McKusick, N. Zinder, A. Levine, R. Roberts, M. Simon, C. Slayman, M. Hunkapiller, Randall A. Bolanos, A. Delcher, I. Dew, D. Fasulo, M. Flanigan, L. Florea, A. Halpern, S. Hannenhalli, S. Kravitz, S. Levy, C. Mobarry, K. Reinert, K. Remington, J. Abu-Threideh, E. Beasley, Kendra Biddick, Vivien R. Bonazzi, R. Brandon, M. Cargill, Ishwar Chandramouliswaran, R. Charlab, Kabir Chaturvedi, Z. Deng, V. D. Francesco, P. Dunn, K. Eilbeck, C. Evangelista, A. Gabrielian, W. Gan, Wangmao Ge, F. Gong, Z. Gu, P. Guan, T. J. Heiman, Maureen E. Higgins, Rui-Ru Ji, Zhaoxi Ke, K. Ketchum, Z. Lai, Yi-Ting Lei, Zhenya Li, Jiayin Li, Yong Liang, Xiaoying Lin, Fu Lu, G. Merkulov, N. Milshina, Helen M. Moore, Ashwinikumar K. Naik, Vaibhav A. Narayan, Beena A. Neelam, D. Nusskern, D. Rusch, S. Salzberg, Wei Shao, B. Shue, Jingtao Sun, Zhen Y. Wang, Aihui Wang, Xin Wang, Jian Wang, M. Wei, R. Wides, Chunlin Xiao, Chunhua Yan, Alison Yao, J. Ye, M. Zhan, Weiqing Zhang, Hongyu Zhang, Qi Zhao, Lian-rong Zheng, F. Zhong, W. Zhong, Shiaoping C. Zhu, Shaying Zhao, Dennis A Gilbert, Suzanna Baumhueter, G. Spier, Christine Carter, A. Cravchik, T. Woodage, Feroze Ali, H. An, A. Awe, D. Baldwin, H. Baden, Mary Barnstead, I. Barrow, K. Beeson, D. Busam, Amy L. Carver, A. Center, Ming-Ming Cheng, Liz Curry, S. Danaher, L. Davenport, Raymond Desilets, S. Dietz, K. Dodson, L. Doup, S. Ferriera, Neha Garg, Andres Gluecksmann, Britney Hart, Jason Haynes, C. Haynes, C. Heiner, S. Hladun, D. Hostin, J. Houck, T. Howland, C. Ibegwam, Jeffery E. Johnson, F. Kalush, Lesley Kline, Shashi B. Koduru, Amy Love, Felecia Mann, D. May, Steven McCawley, T. McIntosh, Ivy McMullen, M. Moy, Linda Moy, B. Murphy, K. Nelson, C. Pfannkoch, Eric C. Pratts, V. Puri, Hina-Ur-Razaq Qureshi, Matt Reardon, Robert Rodriguez, Y. Rogers, Deanna L. Romblad, Bob Ruhfel, Richard T. Scott, Cynthia D. Sitter, Michelle Smallwood, Erin Stewart, R. Strong, Ellen Suh, R. Thomas, Ni Ni Tint, S. Tse, C. Vech, Gary Wang, J. Wetter, Sherita M. Williams, Monica S. Williams, Sandra M. Windsor, E. Winn-Deen, Keriellen Wolfe, J. Zaveri, K. Zaveri, J. F. Abril, R. Guigó, M. Campbell, K. Sjolander, Brian Karlak, A. Kejariwal, H. Mi, B. Lazareva, Thomas Hatton, A. Narechania, Karen Diemer, A. Muruganujan, Nan Guo, Shinji Sato, V. Bafna, S. Istrail, R. Lippert, R. Schwartz, B. Walenz, Shibu Yooseph, D. Allen, A. Basu, J. Baxendale, L. Blick, Marcelo Caminha, John Carnes-Stine, Parris Caulk, Yen-Hui Chiang, My D. Coyne, C. Dahlke, A. D. Mays, M. Dombroski, Michael Donnelly, Dale Ely, Shiva Esparham, C. Fosler, Harold C. Gire, S. Glanowski, K. Glasser, A. Glodek, M. Gorokhov, K. Graham, Barry Gropman, M. Harris, Jeremy Heil, Scott Henderson, Jeffrey Hoover, D. Jennings, Catherine Jordan, J. Jordan, John R. Kasha, Leonid Kagan, C. Kraft, A. Levitsky, Mark Lewis, Xiangjun Liu, John Lopez, Daniel S. Ma, William H. Majoros, J. McDaniel, Sean Murphy, Matthew Newman, Trung Nguyen, N. Nguyen, Marc Nodell, S. Pan, Jim Peck, Marshall W. Peterson, William Rowe, Robert Sanders, J. Scott, M. Simpson, Thomas Smith, A. Sprague, Timothy B. Stockwell, Russell Turner, E. Venter, Mei Wang, M. Wen, David Wu, Mitchell M. Wu, Ashley Xia, A. Zandieh, Xiaohong Zhu +273 moresemanticscholar +7 more sourcesWhole-genome sequencing [PDF]
Practical Neurology, 2021 The costs of whole-genome sequencing have rapidly decreased, and it is being increasingly deployed in large-scale clinical research projects and introduced into routine clinical care. This will lead to rapid diagnoses for patients with genetic disease but also introduces uncertainty because of the diversity of human genomes and the potential ...Huw R Morris, Henry Houlden, James Polkeopenaire +4 more sourcesGenomic sequencing. [PDF]
Proceedings of the National Academy of Sciences, 1984 Unique DNA sequences can be determined directly from mouse genomic DNA. A denaturing gel separates by size mixtures of unlabeled DNA fragments from complete restriction and partial chemical cleavages of the entire genome. These lanes of DNA are transferred and UV-crosslinked to nylon membranes.Church, George, Gilbert, Walteropenaire +4 more sourcesSequencing technologies and genome sequencing [PDF]
Journal of Applied Genetics, 2011 The high-throughput - next generation sequencing (HT-NGS) technologies are currently the hottest topic in the field of human and animals genomics researches, which can produce over 100 times more data compared to the most sophisticated capillary sequencers based on the Sanger method.Pareek, Chandra Shekhar, Smoczyński, Rafał, Tretyn, Andrzej +2 moreopenaire +4 more sourcesOf Mice and Genome Sequence [PDF]
Cell, 2001 Availability of the mouse genome sequence will have a major impact on the study of vertebrate evolution, mammalian biology, and animal models of human disease. Resources to explore genome biology in mice will maximize the effect of this watershed event.Hamilton, B A, Frankel, W Nopenaire +3 more sourcesSequencing the Human Genome [PDF]
Science, 1986 The title of the report by R. Myerowitz and N. Hogikyan on page 1646 of the issue of 27 June was incorrect. It should have been "Different mutations in Ashkenazi Jews and non-Jewish French Canadians with Tay-Sachs disease."James Bruce Walsh, Jon Marksopenaire +6 more sourcesGenome sequences: Genome sequence of a model prokaryote [PDF]
Current Biology, 1997 The complete Escherichia coli genome sequence is now known; it should greatly facilitate the analysis of other genomes, but a lot remains to be learnt about E. coli itself. About half the genes were previously uncharacterized, but expanding databases and improving analysis methods will help predict their functions.openaire +3 more sourcesOn the sequencing of the human genome [PDF]
Proceedings of the National Academy of Sciences, 2002 Two recent papers using different approaches reported draft sequences of the human genome. The international Human Genome Project (HGP) used the hierarchical shotgun approach, whereas Celera Genomics adopted the whole-genome shotgun (WGS) approach. Here, we analyze whether the latter paper provides a meaningful test of the WGS approach on a mammalian ...Waterston, Robert H., Lander, Eric S., Sulston, John E. +2 moreopenaire +3 more sourcesDraft Genome Sequence of Frankia sp. Strain CN3, an Atypical, Noninfective (Nod–) Ineffective (Fix–) Isolate from Coriaria nepalensis [PDF]
, 2013 We report here the genome sequence of Frankia sp. strain CN3, which was isolated from Coriaria nepalensis. This genome sequence is the first from the fourth lineage of Frankia, strains of which are unable to reinfect actinorhizal plants.Beauchemin, Nicholas, Bruce, David, Chain, Patrick, Chen, Amy, Deshpande, Shweta, Detter, Chris, Furnholm, Teal, Ghodhbane-Gtari, Faten, Goodwin, Lynne, Gtari, Maher, Han, Cliff, Han, James, Huntemann, Marcel, Ivanova, Natalia, Kyrpides, Nikos, Land, Miriam L., Markowitz, Victor, Mavrommatis, Kostas, Nolan, Matt, Nouioui, Imen, Pagani, Ioanna, Pati, Amrita, Pitluck, Sam, Santos, Catarina L., Sen, Arnab, Sur, Saubashya, Szeto, Ernest, Tavares, Fernando, Teshima, Hazuki, Thakur, Subarna, Tisa, Louis S., Wall, Luis, Walston Davenport, Karen, Woyke, Tanja +33 morecore +2 more sources