Département de Mathématiques et de Statistiques, Université Laval, Québec, G1K7P4, QC, Canada.
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S52. doi: 10.1186/1471-2156-6-S1-S52.
This paper deals with the detection of significant linkage for quantitative traits using a variance components approach. Microsatellite markers were obtained for the Genetic Analysis Workshop 14 Collaborative Study on the Genetics of Alcoholism data. Ethnic heterogeneity, highly skewed quantitative measures, and a high rate of missing values are all present in this dataset and well known to impact upon linkage analysis. This makes it a good candidate for investigation.
As expected, we observed a number of changes in LOD scores, especially for chromosomes 1, 7, and 18, along with the three factors studied. A dramatic example of such changes can be found in chromosome 7. Highly significant linkage to one of the quantitative traits became insignificant when a proper normalizing transformation of the trait was used and when analysis was carried out on an ethnically homogeneous subset of the original pedigrees.
In agreement with existing literature, transforming a trait to ensure normality using a Box-Cox transformation is highly recommended in order to avoid false-positive linkages. Furthermore, pedigrees should be sorted by ethnic groups and analyses should be carried out separately. Finally, one should be aware that the inclusion of covariates with a high rate of missing values reduces considerably the number of subjects included in the model. In such a case, the loss in power may be large. Imputation methods are then recommended.
本文采用方差分量法检测数量性状的显著连锁。微卫星标记取自遗传分析工作坊 14 关于酒精中毒遗传的协作研究数据。该数据集存在种族异质性、高度偏态的定量测量和高缺失值率,这些都对连锁分析有影响,因此是一个很好的研究对象。
正如预期的那样,我们观察到连锁分析的 LOD 评分发生了一些变化,特别是在染色体 1、7 和 18 以及所研究的三个因素上。这种变化的一个显著例子可以在染色体 7 上找到。当对该性状进行 Box-Cox 转换以确保正态性,并对原始家系的同一种族同质子集进行分析时,一个与一个数量性状高度显著的连锁关系变得不显著。
与现有文献一致,建议使用 Box-Cox 转换对性状进行正态化转换,以避免假阳性连锁。此外,应按种族对家系进行排序,并分别进行分析。最后,应注意到,包含缺失值率较高的协变量会大大减少模型中包含的受试者数量。在这种情况下,可能会出现较大的效能损失。因此建议使用插补方法。