Hsueh W C, Göring H H, Blangero J, Mitchell B D
Department of Genetics, Southwest Foundation for Biomedical Research, P.O. Box 760549, San Antonio, TX 78245, USA.
Genet Epidemiol. 2001;21 Suppl 1:S473-8. doi: 10.1002/gepi.2001.21.s1.s473.
Replication of linkage signals from independent samples is considered an important step toward verifying the significance of linkage signals in studies of complex traits. The purpose of this empirical investigation was to examine the variability in the precision of localizing a quantitative trait locus (QTL) by analyzing multiple replicates of a simulated data set with the use of variance components-based methods. Specifically, we evaluated across replicates the variation in both the magnitude and the location of the peak lod scores. We analyzed QTLs whose effects accounted for 10-37% of the phenotypic variance in the quantitative traits. Our analyses revealed that the precision of QTL localization was directly related to the magnitude of the QTL effect. For a QTL with effect accounting for > 20% of total phenotypic variation, > 90% of the linkage peaks fall within 10 cM from the true gene location. We found no evidence that, for a given magnitude of the lod score, the presence of interaction influenced the precision of QTL localization.
来自独立样本的连锁信号复制被认为是在复杂性状研究中验证连锁信号显著性的重要一步。本实证研究的目的是通过使用基于方差成分的方法分析模拟数据集的多个复制品,来检验定位数量性状基因座(QTL)精度的变异性。具体而言,我们在各复制品中评估了峰值lod分数的大小和位置的变化。我们分析了其效应占数量性状表型方差10%-37%的QTL。我们的分析表明,QTL定位的精度与QTL效应的大小直接相关。对于效应占总表型变异>20%的QTL,>90%的连锁峰值落在距真实基因位置10 cM范围内。我们没有发现证据表明,对于给定大小的lod分数,互作的存在会影响QTL定位的精度。