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改进对个体对之间关系的推断。

Improved inference of relationship for pairs of individuals.

作者信息

Epstein M P, Duren W L, Boehnke M

机构信息

Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Am J Hum Genet. 2000 Nov;67(5):1219-31. doi: 10.1016/S0002-9297(07)62952-8. Epub 2000 Oct 13.

DOI:10.1016/S0002-9297(07)62952-8
PMID:11032786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1288564/
Abstract

Linkage analyses of genetic diseases and quantitative traits generally are performed using family data. These studies assume the relationships between individuals within families are known correctly. Misclassification of relationships can lead to reduced or inappropriately increased evidence for linkage. Boehnke and Cox (1997) presented a likelihood-based method to infer the most likely relationship of a pair of putative sibs. Here, we modify this method to consider all possible pairs of individuals in the sample, to test for additional relationships, to allow explicitly for genotyping error, and to include X-linked data. Using autosomal genome scan data, our method has excellent power to differentiate monozygotic twins, full sibs, parent-offspring pairs, second-degree (2 degrees ) relatives, first cousins, and unrelated pairs but is unable to distinguish accurately among the 2 degrees relationships of half sibs, avuncular pairs, and grandparent-grandchild pairs. Inclusion of X-linked data improves our ability to distinguish certain types of 2 degrees relationships. Our method also models genotyping error successfully, to judge by the recovery of MZ twins and parent-offspring pairs that are otherwise misclassified when error exists. We have included these extensions in the latest version of our computer program RELPAIR and have applied the program to data from the Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus (FUSION) study.

摘要

遗传疾病和数量性状的连锁分析通常使用家系数据进行。这些研究假定家系内个体之间的关系是正确已知的。关系的错误分类可能导致连锁证据减少或不恰当地增加。Boehnke和Cox(1997年)提出了一种基于似然性的方法来推断一对假定同胞最可能的关系。在此,我们对该方法进行修改,以考虑样本中所有可能的个体对,检测其他关系,明确考虑基因分型错误,并纳入X连锁数据。使用常染色体基因组扫描数据,我们的方法在区分同卵双胞胎、全同胞、亲子对、二级亲属、一级表亲以及无关个体对方面具有出色的效能,但无法准确区分半同胞、叔侄对和祖孙对的二级关系。纳入X连锁数据提高了我们区分某些类型二级关系的能力。我们的方法还成功地对基因分型错误进行了建模,这可通过同卵双胞胎和亲子对在存在错误时被误分类后的恢复情况来判断。我们已将这些扩展纳入我们计算机程序RELPAIR的最新版本,并将该程序应用于芬兰 - 美国非胰岛素依赖型糖尿病调查(FUSION)研究的数据。

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