自交系单子对遗传力和连锁方差成分估计的贡献。

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Human Heredity Pub Date : 2018-01-01 Epub Date: 2018-11-02 DOI:10.1159/000492830
Lucy Blondell, August Blackburn, Mark Z Kos, John Blangero, Harald H H Göring
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引用次数: 0

摘要

目的:血缘关系的一个有趣的结果是,近交系的单子成为遗传变异的信息。我们确定了近交系对遗传力和连锁的方差成分分析的贡献。方法:利用数量性状方差成分分析的统计理论,确定近交系单系对遗传力和连锁的似然比检验的预期贡献。结果:在方差成分模型中,近交单例对遗传性测试的贡献相对较小,但对连锁测试的贡献很大。对于小到中等的数量性状位点(QTL)效应和近亲交配的水平(这是许多人类群体中首选的结合形式),近亲繁殖的单子代可以携带非近亲繁殖的兄弟姐妹对的近25%的信息。在实验动物种群、非人类灵长类动物种群和一些人类亚种群的高度近亲繁殖环境中,近亲繁殖的单胎相对于兄弟姐妹的贡献可超过50%。结论:自交系个体,即使与样本的其他成员隔离,也可以有助于方差成分估计和遗传力和连锁的检验。在一定条件下,近交系单子的信息量可以接近非近交系同胞对的信息量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Contribution of Inbred Singletons to Variance Component Estimation of Heritability and Linkage.

Objectives: An interesting consequence of consanguinity is that the inbred singleton becomes informative for genetic variance. We determine the contribution of an inbred singleton to variance component analysis of heritability and linkage.

Methods: Statistical theory for the power of variance component analysis of quantitative traits is used to determine the expected contribution of an inbred singleton to likelihood-ratio tests of heritability and linkage.

Results: In variance component models, an inbred singleton contributes relatively little to a test of heritability but can contribute substantively to a test of linkage. For small-to-moderate quantitative trait locus (QTL) effects and a level of inbreeding comparable to matings between first cousins (the preferred form of union in many human populations), an inbred singleton can carry nearly 25% of the information of a non-inbred sib pair. In more highly inbred contexts available with experimental animal populations, nonhuman primate colonies, and some human subpopulations, the contribution of an inbred singleton relative to a sib pair can exceed 50%.

Conclusions: Inbred individuals, even in isolation from other members of a sample, can contribute to variance component estimation and tests of heritability and linkage. Under certain conditions, the informativeness of the inbred singleton can approach that of a non-inbred sib pair.

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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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