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Missing phenotype data imputation in pedigree data analysis.

机译:在谱系数据分析中缺少表型数据插补。

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摘要

Mapping complex traits or phenotypes with small genetic effects, whose phenotypes may be modulated by temporal trends in families are challenging. Detailed and accurate data must be available on families, whether or not the data were collected over time. Missing data complicate matters in pedigree analysis, especially in the case of a longitudinal pedigree analysis. Because most analytical methods developed for the analysis of longitudinal pedigree data require no missing data, the researcher is left with the option of dropping those cases (individuals) with missing data from the analysis or imputing values for the missing data. We present the use of data augmentation within Bayesian polygenic and longitudinal polygenic models to produce k complete datasets. The data augmentation, or imputation step of the Markov chain Monte Carlo, takes into account the observed familial information and the observed subject information available at other time points. These k complete datasets can then be used to fit single time point or longitudinal pedigree models. By producing a set of k complete datasets and thus k sets of parameter estimates, the total variance associated with an estimate can be partitioned into a within-imputation and a between-imputation component. The method is illustrated using the Genetic Analysis Workshop simulated data. Genet. Epidemiol. 2007. (c) 2007 Wiley-Liss, Inc.
机译:映射具有较小遗传效应的复杂性状或表型,其表型可能受到家庭时间趋势的调节,这具有挑战性。无论是否随时间收集数据,都必须提供有关家庭的详细而准确的数据。缺少数据会使谱系分析变得复杂,尤其是在纵向谱系分析的情况下。因为开发用于分析纵向谱系数据的大多数分析方法都不需要缺失数据,所以研究人员可以选择从分析中删除具有缺失数据的案例(个人)或为缺失数据估算值。我们目前在贝叶斯多基因和纵向多基因模型内使用数据增强来产生k个完整的数据集。马尔可夫链蒙特卡洛的数据扩充或估算步骤考虑了观察到的家族信息和在其他时间点可用的观察到的受试者信息。然后,可以使用这k个完整的数据集来拟合单个时间点或纵向谱系模型。通过生成一组k个完整的数据集,从而生成k组参数估计值,可以将与估计值相关的总方差划分为输入内分量和输入间分量。使用遗传分析研讨会仿真数据说明了该方法。基因流行病。 2007(c)2007 Wiley-Liss,Inc.

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