| Literature DB >> 18251251 |
Lise Lotte Hansen1, Bo Eskerod Madsen, Kristina Pedersen, Carsten Wiuf.
Abstract
Single nucleotide polymorphisms (SNPs) are highly abundant in the genome and especially useful in the search for disease susceptibility genes via population-based association or linkage studies. Therefore, there is a strong need for high throughput and reliable methodologies to assess the SNP genotypes. Despite an unambiguous result of an SNP analysis, with the use of a commercial kit based on primer extension, subsequent sequencing analysis revealed that a proportion of the genotypes was not correctly assessed. The problem we have encountered may originate from specific structures in the genomic DNA sequence, rather than being a methodological problem.Mesh:
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Year: 2007 PMID: 18251251 DOI: 10.2144/000112675
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993