Closing gaps in the human genome with fosmid resources generated from multiple individuals-Reference-Cited by-同舟云学术

Closing gaps in the human genome with fosmid resources generated from multiple individuals

Published:2007-12-23 Issue:1 Volume:40 Page:96-101
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Bovee Donald,Zhou Yang,Haugen Eric,Wu Zaining,Hayden Hillary S,Gillett Will,Tuzun Eray,Cooper Gregory M,Sampas Nick,Phelps Karen,Levy Ruth,Morrison V Anne,Sprague James,Jewett Donald,Buckley Danielle,Subramaniam Sandhya,Chang Jean,Smith Douglas R,Olson Maynard V,Eichler Evan E,Kaul Rajinder

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2007.34.pdf

Reference27 articles.

1. International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome. Nature 431, 931–945 (2004).

2. Eichler, E.E., Clark, R.A. & She, X. An assessment of the sequence gaps: unfinished business in a finished human genome. Nat. Rev. Genet. 5, 345–354 (2004).

3. Bailey, J.A. et al. Recent segmental duplications in the human genome. Science 297, 1003–1007 (2002).

4. Istrail, S. et al. Whole genome shotgun assembly and comparison of human genome assemblies. Proc. Natl. Acad. Sci. USA 101, 1916–1921 (2004).

5. Sebat, J. et al. Large-scale copy number polymorphism in human genome. Science 305, 525–528 (2004).

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