首页> 美国卫生研究院文献>other >A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
【2h】

A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study

机译:潜在变量偏最小二乘路径建模方法对区域协会和多基因遗传的影响与应用到人类肥胖的研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Genetic association studies are now routinely used to identify single nucleotide polymorphisms (SNPs) linked with human diseases or traits through single SNP-single trait tests. Here we introduced partial least squares path modeling (PLSPM) for association between single or multiple SNPs and a latent trait that can involve single or multiple correlated measurement(s). Furthermore, the framework naturally provides estimators of polygenic effect by appropriately weighting trait-attributing alleles. We conducted computer simulations to assess the performance via multiple SNPs and human obesity-related traits as measured by body mass index (BMI), waist and hip circumferences. Our results showed that the associate statistics had type I error rates close to nominal level and were powerful for a range of effect and sample sizes. When applied to 12 candidate regions in data (N = 2,417) from the European Prospective Investigation of Cancer (EPIC)-Norfolk study, a region in FTO was found to have stronger association (rs7204609∼rs9939881 at the first intron P = 4.29×10−7) than single SNP analysis (all with P>10−4) and a latent quantitative phenotype was obtained using a subset sample of EPIC-Norfolk (N = 12,559). We believe our method is appropriate for assessment of regional association and polygenic effect on a single or multiple traits.
机译:遗传结合研究现在经常用于通过单一SNP单一特征试验鉴定与人类疾病或特征有关的单核苷酸多态性(SNP)。在这里,我们引入了部分最小二乘路径建模(PLSPM)以便在单个或多个SNP之间的关联和可以涉及单个或多个相关测量的潜在特征。此外,该框架通过适当加权归属等位基因来自然提供多种基因效果的估计。我们进行了计算机模拟,以通过体重指数(BMI),腰部和臀部圆周测量​​的多个SNP和人类肥胖相关性能来评估性能。我们的研究结果表明,助理统计数据型I型误差率接近标称级别,对于一系列效果和样本尺寸而强大。当从欧洲癌症(EPIC)-OORFOLK研究中的数据(n = 2,417)中的数据(n = 2,417)中的12个候选地区,发现FTO中的一个区域具有更强的关联(第一个内含子P = 4.29×10的rs7204609~rs9939881 -7 )比单个SNP分析(所有具有p> 10 -4-4)和使用epic-norfolk的子集样品获得潜在的定量表型(n = 12,559) 。我们认为我们的方法适用于对单一或多种特征的区域关联和多种子基因的评估。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号