학술논문
Whole-genome shotgun assembly and comparison of human genome assemblies
Document Type
Author Abstract
Author
Istrail, Sorin; Sutton, Granger G.; Florea, Liliana; Halpern, Aaron L.; Mobarry, Clark M.; Lippert, Ross; Walenz, Brian; Shatkay, Hagit; Dew, Ian; Miller, Jason R.; Flanigan, Michael J.; Edwards, Nathan J.; Bolanos, Randall; Fasulo, Daniel; Halldorsson, Bjarni V.; Hannenhalli, Sridhar; Turner, Russell; Yooseph, Shibu; Lu, Fu; Nusskern, Deborah R.; Shue, Bixiong Chris; Zheng, Xiangqun Holly; Zhong, Fei; Delcher, Arthur L.; Huson, Daniel H.; Kravitz, Saul A.; Mouchard, Laurent; Reinert, Knut; Remington, Karin A.; Clark, Andrew G.; Waterman, Michael S.; Eichler, Evan E.; Adams, Mark D.; Hunkapiller, Michael W.; Myers, Eugene W.; Venter, J. Craig
Source
Proceedings of the National Academy of Sciences of the United States. Feb 17, 2004, Vol. 101 Issue 7, p1916, 6 p.
Subject
Language
English
ISSN
0027-8424
Abstract
We report a whole-genome shotgun assembly (called WGSA) of the human genome generated at Celera in 2001. The Celera-generated shotgun data set consisted of 27 million sequencing reads organized in pairs by virtue of end-sequencing 2-kbp, 10-kbp, and 50-kbp inserts from shotgun clone libraries. The quality-trimmed reads covered the genome 5.3 times, and the inserts from which pairs of reads were obtained covered the genome 39 times. With the nearly complete human DNA sequence [National Center for Biotechnology Information (NCBI) Build 34] now available, it is possible to directly assess the quality, accuracy, and completeness of WGSA and of the first reconstructions of the human genome reported in two landmark papers in February 2001 [Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) Science 291, 1304-1351; International Human Genome Sequencing Consortium (2001) Nature 409, 860-921]. The analysis of WGSA shows 97% order and orientation agreement with NCBI Build 34, where most of the 3% of sequence out of order is due to scaffold placement problems as opposed to assembly errors within the scaffolds themselves. In addition, WGSA fills some of the remaining gaps in NCBI Build 34. The early genome sequences all covered about the same amount of the genome, but they did so in different ways. The Celera results provide more order and orientation, and the consortium sequence provides better coverage of exact and nearly exact repeats.