## Abstract Genotype error can greatly reduce the power of a genetic study. For family data, genotype error can be assessed by examining marker data for nonβMendelian inconsistencies, closely linked markers for double recombination events, and consistency of duplicate genotypes. For caseβcontrol da
Proofreading genotyping assays and electrochemical detection of SNPs
β Scribed by Garry C. King; Daniel A. Di Giusto; Wjatschesslaw A. Wlassoff; Susanne Giesebrecht; Eleanor Flening; Gregory D. Tyrelle
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 172 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1059-7794
No coin nor oath required. For personal study only.
β¦ Synopsis
For the Mutation Detection 2003 Special Issue
The use of proofreading DNA polymerases in genotyping assays offers the prospect of improved performance.
To this end, we have recently used compatible DNA polymerases, protected primers, and substrates to implement proofreading single base extension (P-SBE) and proofreading allele-specific extension (PRASE) assays. Key aspects of the P-SBE and related proofreading assay formats are described here. For transduction of genotyping reactions into physical signals, electrochemical SBE implementations may offer simple, inexpensive assays in electrode array or electrophoretic formats. We have developed electrochemically-labeled nucleotides and electrode detection methods with a view to these applications. Detection of electrochemically-labeled SBE products on an oligonucleotide-modified gold electrode surface is demonstrated. Hum Mutat 23:420-425, 2004 r 2004 Wiley-Liss, Inc.
π SIMILAR VOLUMES
## Communicated by Ann-Christine Syva Β¨nen Utilizing the results of extensive single nucleotide polymorphism (SNP) studies in humans, stimulated by the International HapMap Project, we present evidence that SNPs are not randomly spaced across the genome, but are somewhat clustered. This observatio