Murray Sarah Shaw, Oliphant Arnold, Shen Richard, McBride Celeste, Steeke Rhoberta J, Shannon Stuart G, Rubano Todd, Kermani Bahram G, Fan Jian-Bing, Chee Mark S, Hansen Mark S T
Illumina, Inc., 9885 Towne Centre Drive, San Diego, California 92121-1975, USA.
Nat Methods. 2004 Nov;1(2):113-7. doi: 10.1038/nmeth712. Epub 2004 Oct 21.
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.
我们开发了一套信息量丰富的单核苷酸多态性(SNP)检测方法,用于人类基因组的连锁图谱绘制。这些检测方法是在一个强大的多重检测系统上开发的,旨在为连锁研究提供极高的准确性、数据完整性以及高通量的组合。该连锁分析板由约4700个SNP组成,平均次要等位基因频率为0.39,平均间距为624 kb。基于近200万个基因型,数据质量显示极高,检出率为99.94%,重复性>99.99%,且99.995%的基因型符合孟德尔遗传规律。我们使用28个CEPH家系构建了平均分辨率为1.5 cM的遗传图谱。该分析板的相对信息含量高于常用的STR标记分析板。这种SNP连锁分析板与多重检测系统的有效结合为连锁研究提供了前所未有的性能水平。