{"title":"Statistically efficient association analysis of quantitative traits with haplotypes and untyped SNPs in family studies.","authors":"Guoqing Diao, Dan-Yu Lin","doi":"10.1186/s12863-020-00902-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Associations between haplotypes and quantitative traits provide valuable information about the genetic basis of complex human diseases. Haplotypes also provide an effective way to deal with untyped SNPs. Two major challenges arise in haplotype-based association analysis of family data. First, haplotypes may not be inferred with certainty from genotype data. Second, the trait values within a family tend to be correlated because of common genetic and environmental factors.</p><p><strong>Results: </strong>To address these challenges, we present an efficient likelihood-based approach to analyzing associations of quantitative traits with haplotypes or untyped SNPs. This approach properly accounts for within-family trait correlations and can handle general pedigrees with arbitrary patterns of missing genotypes. We characterize the genetic effects on the quantitative trait by a linear regression model with random effects and develop efficient likelihood-based inference procedures. Extensive simulation studies are conducted to examine the performance of the proposed methods. An application to family data from the Childhood Asthma Management Program Ancillary Genetic Study is provided. A computer program is freely available.</p><p><strong>Conclusions: </strong>Results from extensive simulation studies show that the proposed methods for testing the haplotype effects on quantitative traits have correct type I error rates and are more powerful than some existing methods.</p>","PeriodicalId":9197,"journal":{"name":"BMC Genetics","volume":" ","pages":"99"},"PeriodicalIF":2.9000,"publicationDate":"2020-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487716/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12863-020-00902-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Associations between haplotypes and quantitative traits provide valuable information about the genetic basis of complex human diseases. Haplotypes also provide an effective way to deal with untyped SNPs. Two major challenges arise in haplotype-based association analysis of family data. First, haplotypes may not be inferred with certainty from genotype data. Second, the trait values within a family tend to be correlated because of common genetic and environmental factors.
Results: To address these challenges, we present an efficient likelihood-based approach to analyzing associations of quantitative traits with haplotypes or untyped SNPs. This approach properly accounts for within-family trait correlations and can handle general pedigrees with arbitrary patterns of missing genotypes. We characterize the genetic effects on the quantitative trait by a linear regression model with random effects and develop efficient likelihood-based inference procedures. Extensive simulation studies are conducted to examine the performance of the proposed methods. An application to family data from the Childhood Asthma Management Program Ancillary Genetic Study is provided. A computer program is freely available.
Conclusions: Results from extensive simulation studies show that the proposed methods for testing the haplotype effects on quantitative traits have correct type I error rates and are more powerful than some existing methods.
背景:单倍型与数量性状之间的关联为复杂人类疾病的遗传基础提供了宝贵的信息。单倍型也是处理无类型 SNP 的有效方法。基于单倍型的家系数据关联分析面临两大挑战。首先,单倍型可能无法从基因型数据中确定地推断出来。其次,由于共同的遗传和环境因素,一个家族内的性状值往往是相关的:为了应对这些挑战,我们提出了一种基于似然法的高效方法,用于分析数量性状与单倍型或非类型 SNP 的关联。这种方法能适当考虑家系内的性状相关性,并能处理具有任意缺失基因型模式的一般系谱。我们通过随机效应线性回归模型来描述对数量性状的遗传效应,并开发了高效的基于似然法的推断程序。我们进行了广泛的模拟研究,以检验所提出方法的性能。研究还提供了儿童哮喘管理计划辅助基因研究中家庭数据的应用。计算机程序免费提供:广泛的模拟研究结果表明,所提出的检验单倍型对数量性状影响的方法具有正确的 I 型错误率,比现有的一些方法更强大。
期刊介绍:
BMC Genetics is an open access, peer-reviewed journal that considers articles on all aspects of inheritance and variation in individuals and among populations.