Division of Biostatistics and Bioinformatics, National Health Research Institutes, Miaoli, Taiwan, ROC.
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S89. doi: 10.1186/1471-2156-6-S1-S89.
We conducted genome-wide linkage scans using both microsatellite and single-nucleotide polymorphism (SNP) markers. Regions showing the strongest evidence of linkage to alcoholism susceptibility genes were identified. Haplotype analyses using a sliding-window approach for SNPs in these regions were performed. In addition, we performed a genome-wide association scan using SNP data. SNPs in these regions with evidence of association (P <or= 0.0001) were identified. We found that the general patterns for nonparametric linkage (NPL) scores from SNP and microsatellite genome scans are fairly consistent; however, the peaks of the NPL scores are mostly higher in the SNP-based scan than those using microsatellite markers, which might be located at different regions. Furthermore, SNPs identified from linkage screens were not so strongly associated with alcoholism (the most significant SNP had a p-value of 0.030) as those identified from association genomic screening (the most significant SNP had a p-value of 2.0 x 10(-8)).
我们使用微卫星和单核苷酸多态性 (SNP) 标记进行了全基因组连锁扫描。确定了与酒精中毒易感性基因最强连锁证据的区域。对这些区域中 SNP 进行了滑动窗口方法的单体型分析。此外,我们还使用 SNP 数据进行了全基因组关联扫描。确定了具有关联证据的这些区域中的 SNP(P <= 0.0001)。我们发现,来自 SNP 和微卫星基因组扫描的非参数连锁 (NPL) 分数的总体模式相当一致;然而,基于 SNP 的扫描中的 NPL 分数峰值大多高于使用微卫星标记的那些,这可能位于不同的区域。此外,从连锁屏幕中鉴定的 SNP 与酒精中毒的相关性不如从关联基因组筛选中鉴定的 SNP 强(最显著的 SNP 的 p 值为 0.030)(最显著的 SNP 的 p 值为 2.0 x 10(-8))。