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Published online before print
March 12, 2003, 10.1101/gr.886203
METHODS Efficient High-Throughput Resequencing of Genomic DNAWashington 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. 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.
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