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Correlation between Relatives given Complete Genotypes: from Identity by Descent to Identity by Function

机译:给定完整基因型的亲戚之间的相关性:从后裔身份到功能身份

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摘要

In classical quantitative genetics, the correlation between the phenotypes of individuals with unknown genotypes and a known pedigree relationship is expressed in terms of probabilities of IBD states. In existing approaches to the inverse problem where genotypes are observed but pedigree relationships are not, dependence between phenotypes is either modeled as Bayesian uncertainty or mapped to an IBD model via inferred relatedness parameters. Neither approach yields a relationship between genotypic similarity and phenotypic similarity with a probabilistic interpretation corresponding to a generative model. We introduce a generative model for diploid allele effect based on the classic infinite allele mutation process. This approach motivates the concept of IBF (Identity by Function). The phenotypic covariance between two individuals given their diploid genotypes is expressed in terms of functional identity states. The IBF parameters define a genetic architecture for a trait without reference to specific alleles or population. Given full genome sequences, we treat a gene-scale functional region, rather than a SNP, as a QTL, modeling patterns of dominance for multiple alleles. Applications demonstrated by simulation include phenotype and effect prediction and association, and estimation of heritability and classical variance components. A simulation case study of the Missing Heritability problem illustrates a decomposition of heritability under the IBF framework into Explained and Unexplained components.
机译:在经典的定量遗传学中,基因型未知的个体的表型与已知的谱系关系之间的相关性以IBD状态的概率表示。在观察到基因型但没有谱系关系的反问题的现有方法中,将表型之间的依赖性建模为贝叶斯不确定性或通过推断的相关性参数映射到IBD模型。两种方法都不会在基因型相似性和表型相似性之间产生与对应于生成模型的概率解释之间的关系。我们介绍了基于经典无限等位基因突变过程的二倍体等位基因效应的生成模型。这种方法激发了IBF(身份按功能)的概念。给定其二倍体基因型的两个个体之间的表型协方差以功能同一性状态表示。 IBF参数定义了性状的遗传结构,而无需参考特定的等位基因或种群。给定完整的基因组序列,我们将基因规模的功能区而不是SNP视为QTL,为多个等位基因建立优势模式。通过仿真证明的应用包括表型和效果预测与关联,以及遗传力和经典方差分量的估计。对遗失性遗传问题的模拟案例研究表明,在IBF框架下,遗传性分解为解释性和无法解释性的组件。

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