Xing Jinchuan, Watkins W Scott, Zhang Yuhua, Witherspoon David J, Jorde Lynn B
Department of Human Genetics, Eccles Institute of Human Genetics, University of Utah, Salt Lake City, UT, 84112, USA.
Genomics. 2008 Dec;92(6):452-6. doi: 10.1016/j.ygeno.2008.08.007. Epub 2008 Sep 27.
Current microarray technology allows researchers to genotype a large number of SNPs with relatively small amounts of DNA. Nevertheless, researchers and clinicians still frequently face the problem of acquiring enough high-quality DNA for analysis. Whole-genome amplification (WGA) methods offer a solution for this problem, and earlier studies have shown that WGA samples perform reasonably well in small-scale genetic analyses (e.g. Affymetrix 10K array). To determine the performance of WGA products on a large-scale genotyping array, we compared the Affymetrix 250K array genotyping results of genomic DNA and their WGA products from four individuals. Our results indicate that WGA product performs well on the 250K array compared to genomic DNA, especially when using the BRLMM calling algorithm. WGA samples have high call rates (97.5% on average, compared to 99.4% for genomic DNA) and excellent concordance rates with their corresponding genomic DNA samples (98.7% on average). In addition, no apparent systematic genomic amplification bias can be detected. This study demonstrates that, although there is a slight decrease in the total call rates, WGA methods provide a reliable approach for increasing the amount of DNA samples for use with a common SNP genotyping array.
当前的微阵列技术使研究人员能够用相对少量的DNA对大量单核苷酸多态性(SNP)进行基因分型。然而,研究人员和临床医生仍然经常面临获取足够高质量DNA用于分析的问题。全基因组扩增(WGA)方法为解决这一问题提供了一种方案,早期研究表明,WGA样本在小规模基因分析(如Affymetrix 10K芯片)中表现良好。为了确定WGA产物在大规模基因分型芯片上的性能,我们比较了来自四个个体的基因组DNA及其WGA产物在Affymetrix 250K芯片上的基因分型结果。我们的结果表明,与基因组DNA相比,WGA产物在250K芯片上表现良好,尤其是在使用BRLMM调用算法时。WGA样本具有较高的检出率(平均97.5%,而基因组DNA为99.4%),并且与其相应的基因组DNA样本具有出色的一致性率(平均98.7%)。此外,未检测到明显的系统性基因组扩增偏差。这项研究表明,尽管总检出率略有下降,但WGA方法为增加用于常见SNP基因分型芯片的DNA样本量提供了一种可靠的方法。