首页> 美国卫生研究院文献>G3: GenesGenomesGenetics >Genome-Wide Association Study in Two Cohorts from a Multi-generational Mouse Advanced Intercross Line Highlights the Difficulty of Replication Due to Study-Specific Heterogeneity
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Genome-Wide Association Study in Two Cohorts from a Multi-generational Mouse Advanced Intercross Line Highlights the Difficulty of Replication Due to Study-Specific Heterogeneity

机译:来自多代小鼠高级交叉谱系的两个队列的全基因组关联研究突出了由于研究特定的异质性而导致的复制困难

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摘要

There has been extensive discussion of the “Replication Crisis” in many fields, including genome-wide association studies ( ). We explored replication in a mouse model using an advanced intercross line ( ), which is a multigenerational intercross between two inbred strains. We re-genotyped a previously published cohort of LG/J x SM/J AIL mice (F ; n = 428) using a denser marker set and genotyped a new cohort of AIL mice (F ; n = 600) for the first time. We identified 36 novel genome-wide significant loci in the F and 25 novel loci in the F cohort. The subset of traits that were measured in both cohorts (locomotor activity, body weight, and coat color) showed high genetic correlations, although the SNP heritabilities were slightly lower in the F cohort. For this subset of traits, we attempted to replicate loci identified in either F or F in the other cohort. Coat color was robustly replicated; locomotor activity and body weight were only partially replicated, which was inconsistent with our power simulations. We used a random effects model to show that the partial replications could not be explained by Winner’s Curse but could be explained by study-specific heterogeneity. Despite this heterogeneity, we performed a mega-analysis by combining F and F cohorts (n = 1,028), which identified four novel loci associated with locomotor activity and body weight. These results illustrate that even with the high degree of genetic and environmental control possible in our experimental system, replication was hindered by study-specific heterogeneity, which has broad implications for ongoing concerns about reproducibility.
机译:在许多领域,包括全基因组关联研究(),都对“复制危机”进行了广泛的讨论。我们使用高级交叉线()探索了小鼠模型中的复制,该交叉线是两个近交菌株之间的多代交叉。我们使用更密集的标记集对先前发表的LG / J x SM / J AIL小鼠队列(F; n = 428)进行基因分型,并首次对新的AIL小鼠队列(F; n = 600)进行基因分型。我们确定了F中的36个新的基因组范围内的重要基因座和F队列中的25个新的基因座。在两个队列中测量的性状的子集(运动能力,体重和毛色)显示出高度的遗传相关性,尽管在F队列中SNP遗传力略低。对于此特征子集,我们尝试复制在另一个队列中的F或F中识别出的基因座。外套颜色被强烈复制;运动活动和体重仅被部分复制,这与我们的功率模拟不一致。我们使用随机效应模型表明,部分重复不能由Winner的诅咒来解释,而可以由特定于研究的异质性来解释。尽管存在这种异质性,我们还是通过结合F和F队列(n = 1,028)进行了大规模分析,该队列确定了四个与运动活动和体重相关的新基因座。这些结果说明,即使在我们的实验系统中可能进行高度的遗传和环境控制,复制仍会受到特定于研究的异质性的阻碍,异质性对人们对可重复性的持续关注具有广泛的意义。

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