| Literature DB >> 15782173 |
Sarah Shaw Murray1, Arnold Oliphant, Richard Shen, Celeste McBride, Rhoberta J Steeke, Stuart G Shannon, Todd Rubano, Bahram G Kermani, Jian-Bing Fan, Mark S Chee, Mark S T Hansen.
Abstract
We have developed a highly informative set of single-nucleotide polymorphism (SNP) assays designed for linkage mapping of the human genome. These assays were developed on a robust multiplexed assay system to provide a combination of very high accuracy and data completeness with high throughput for linkage studies. The linkage panel is comprised of approximately 4,700 SNPs with 0.39 average minor allele frequency and 624-kb average spacing. Based on almost 2 million genotypes, data quality was shown to be extremely high, with a 99.94% call rate, >99.99% reproducibility and 99.995% genotypes consistent with mendelian inheritance. We constructed a genetic map with an average 1.5-cM resolution using series of 28 CEPH pedigrees. The relative information content of this panel was higher than those of commonly used STR marker panels. The potent combination of this SNP linkage panel with the multiplexed assay system provides a previously unattainable level of performance for linkage studies.Entities:
Mesh:
Year: 2004 PMID: 15782173 DOI: 10.1038/nmeth712
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547