Genome Research scroll

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Published online before print March 12, 2003, 10.1101/gr.886203
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
GR-8862Rv1
13/4/717    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Miller, R. D.
Right arrow Articles by Kwok, P.-Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Miller, R. D.
Right arrow Articles by Kwok, P.-Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Vol 13, Issue 4, 717-720, April 2003

METHODS

Efficient High-Throughput Resequencing of Genomic DNA

Raymond D. Miller, Shenghui Duan, Elizabeth G. Lovins1, Ellen F. Kloss and Pui-Yan Kwok1,2

Washington University, Division of Dermatology, St. Louis, Missouri 63110, USA

Targeted resequencing of genomic DNA from organisms such as humans is an important tool enabling experimental access to variation within the species and between similar species. Taking full advantage of the reference genome sequences in designing robust, specific PCR assays and using stringent conditions, resequencing can be done efficiently without purification of the PCR product. By using a 10-fold greater amount of one primer when setting up the PCR initially in a new version of asymmetric PCR, one simply adds the rest of the sequencing reagents at the end of PCR and allows the sequencing reaction to proceed, with the excess PCR primer serving as the sequencing primer. We demonstrated that this streamlined protocol can be used with PCR products up to 1300 bp and had up to a 97% success rate in high-throughput analysis of allele frequencies for >30,000 single-nucleotide polymorphisms (SNPs). SNP primers and characterization results are provided at http://snp.wustl.edu.


1 Present address: University of California, San Francisco, Cardiovascular Research Institute, San Francisco, California 94143-0130, USA.

2 Corresponding author.

E-MAIL kwok{at}cvrimail.ucsf.edu; FAX (415) 476-2283.

Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.886203. Article published online before print in March 2003.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
N. Whiteford, N. Haslam, G. Weber, A. Prugel-Bennett, J. W. Essex, P. L. Roach, M. Bradley, and C. Neylon
An analysis of the feasibility of short read sequencing
Nucleic Acids Res., November 7, 2005; 33(19): e171 - e171.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
P. R. Haddrill, K. R. Thornton, B. Charlesworth, and P. Andolfatto
Multilocus patterns of nucleotide variability and the demographic and selection history of Drosophila melanogaster populations
Genome Res., June 1, 2005; 15(6): 790 - 799.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
R. L. Margraf, S. Page, M. Erali, and C. T. Wittwer
Single-Tube Method for Nucleic Acid Extraction, Amplification, Purification, and Sequencing
Clin. Chem., October 1, 2004; 50(10): 1755 - 1761.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
D. L. Halligan, A. Eyre-Walker, P. Andolfatto, and P. D. Keightley
Patterns of Evolutionary Constraints in Intronic and Intergenic DNA of Drosophila
Genome Res., February 1, 2004; 14(2): 273 - 279.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
J. W. Watters, E. F. Kloss, D. C. Link, T. A. Graubert, and H. L. McLeod
A mouse-based strategy for cyclophosphamide pharmacogenomic discovery
J Appl Physiol, October 1, 2003; 95(4): 1352 - 1360.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Genes Dev. Learn. Mem.
Protein Science RNA Genome Res.