Single Nucleotide Polymorphism Mapping Using Genome-Wide Unique Sequences
Abstract
As more and more genomic DNAs are sequenced to characterize human genetic variations, the demand for a very fast and accurate method to genomically position these DNA sequences is high. We have developed a new mapping method that does not require sequence alignment. In this method, we first identified DNA fragments of 15 bp in length that are unique in the human genome and then used them to position single nucleotide polymorphism (SNP) sequences. By use of four desktop personal computers with AMD K7 (1 GHz) processors, our new method mapped more than 1.6 million SNP sequences in 20 hr and achieved a very good agreement with mapping results from alignment-based methods.
Footnotes
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↵1 Corresponding author.
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E-MAIL mjhwang{at}ibms.sinica.edu.tw; FAX (886) 2-2788-7641.
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Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.224502. Article published online before print in June 2002.
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- Received November 19, 2001.
- Accepted April 8, 2002.
- Cold Spring Harbor Laboratory Press
