首页> 外文会议>Lateral Thinking: The Evolution of Human Handedness (Workshop) >Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies
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Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies

机译:手中的多层遗传模型在解释家庭数据并与基因组关联研究兼容时非常类似于单轨模型

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Right- and left-handedness run in families, show greater concordance in monozygotic than dizygotic twins, and are well described by single-locus Mendelian models. Here we summarize a large genome-wide association study (GWAS) that finds no significant associations with handedness and is consistent with a meta-analysis of GWASs. The GWAS had 99% power to detect a single locus using the conventional criterion of P < 5 × 10~(?8) for the single locusmodels ofMcManus and Annett. The strong conclusion is that handedness is not controlled by a single genetic locus. A consideration of the genetic architecture of height, primary ciliary dyskinesia, and intelligence suggests that handedness inheritance can be explained by a multilocus variant of the McManus DC model, classical effects on family and twins being barely distinguishable from the single locus model. Based on the ENGAGE meta-analysis of GWASs, we estimate at least 40 loci are involved in determining handedness.
机译:右手和左撇子在家庭中运行,在单一程度上表现出更大的一致性,而不是Dizygotic Twins,并通过单个轨道孟德尔模型进行了很好的描述。在这里,我们总结了一个大型基因组关联研究(GWA),该研究没有与手腕的显着关联,并且与Gwass的Meta分析一致。 GWA有99%的动力来检测单个基因座,用于使用Manus和Annett的单个LocusModels的P <5×10〜(?8)的传统标准。强烈的结论是,手中不受单一遗传基因座控制。考虑到高度,主要睫状体障碍和智力的遗传建筑,表明,手工遗传可以通过McManus DC模型的多点变种来解释,对家庭和双胞胎的古典效果从单个基因座模型几乎没有区分。基于GWAS的接合元分析,我们估计至少40个基因座参与了决定性的。

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