Automatable SNP assay
-
Correspondence: Jonathan B Weitzman jonathanweitzman@hotmail.com
Genome Biology 2001, 2:spotlight-20010227-01 doi:10.1186/gb-spotlight-20010227-01
The electronic version of this article is the complete one and can be found online at:
| Published: | 27 February 2001 |
© 2001 BioMed Central Ltd
Research news
In the February 27 Proceedings of the National Academy of Sciences, Bartlett et al. describe a simple technique for single-nucleotide polymorphism (SNP) analysis that could be easily automated for high-throughput SNP typing (Proc Natl Acad Sci USA 2001, 98:2694-2697). The fluorescence technique (which the authors dub ADMI, alkaline-mediated differential interaction) is adapted from the amplification-refractory mutation system (ARMS)-PCR and exploits the double-stranded DNA-specific dye SYBR green I, combined with detection at buffered high pH conditions. The technique is inexpensive, automatable, simple and robust, making it ideal for high-throughput applications. Bartlett et al. tested the performance of the assay using 32 sequence-specific primer mixes to identify HLA genotypes of 80 independent lymphoblastoid cell lines.
References
-
Proceedings of the National Academy of Sciences
-
[http://www.ncbi.nlm.nih.gov/SNP/index.html] webcite
A Database of Single Nucleotide Polymorphisms
-
Tissue typing the HLA-A locus from genomic DNA by sequence-specific PCR: comparison of HLA genotype and surface expression on colorectal tumor cell lines.
PubMed Abstract | Publisher Full Text | PubMed Central Full Text