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Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

机译:带有估算变异的遗传方差估计发现人体高度和体重指数的遗漏遗传力可以忽略不计

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摘要

We propose a method (GREML-LDMS) to estimate heritability for human complex traits in unrelated individuals using whole-genome sequencing data. We demonstrate using simulations based on whole-genome sequencing data that similar to 97% and similar to 68% of variation at common and rare variants, respectively, can be captured by imputation. Using the GREML-LDMS method, we estimate from 44,126 unrelated individuals that all similar to 17 million imputed variants explain 56% (standard error (s.e.) = 2.3%) of variance for height and 27% (s.e. = 2.5%) of variance for body mass index (BMI), and we find evidence that height- and BMI-associated variants have been under natural selection. Considering the imperfect tagging of imputation and potential overestimation of heritability from previous family-based studies, heritability is likely to be 60-70% for height and 30-40% for BMI. Therefore, the missing heritability is small for both traits. For further discovery of genes associated with complex traits, a study design with SNP arrays followed by imputation is more cost-effective than whole-genome sequencing at current prices.
机译:我们提出了一种方法(GREML-LDMS),使用全基因组测序数据来估计无关个体中人类复杂性状的遗传力。我们证明了使用基于全基因组测序数据的模拟,通过插补可以分别捕获到普通变异和稀有变异中相似变异的97%和相似变异的68%。使用GREML-LDMS方法,我们从44,126个无亲缘关系的个体中估计,所有与1700万个估算变量相似的变量解释了高度的56%(标准误(se)= 2.3%)和27%(se = 2.5%)的方差。体重指数(BMI),我们发现有证据表明与身高和BMI相关的变异已处于自然选择之下。考虑到以前的基于家族的研究中归因标记的不完善和对遗传力的潜在高估,身高的遗传力很可能为60-70%,而BMI的遗传力可能为30-40%。因此,两种性状的缺失遗传力均较小。为了进一步发现与复杂性状相关的基因,采用SNP阵列并进行插补的研究设计比按当前价格进行全基因组测序更具成本效益。

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