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两种常用数量性状连锁分析方法的原理和进展
引用本文:宿少勇,顾东风.两种常用数量性状连锁分析方法的原理和进展[J].遗传,2004,26(2):253-256.
作者姓名:宿少勇  顾东风
作者单位:中国医学科学院 中国协和医科大学 阜外心血管病医院 群体遗传与人群防治研究室,北京 100037 Division of Population Genetics and Prevention, Cardiovascular Institute & Fu Wai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100037, China
摘    要:在复杂性状疾病的家系连锁研究中,Haseman-Elston回归分析和方差组成模型是常用的两种数量性状连锁分析方法。前者主要针对同胞对的性状值差或和的平方进行回归分析;后者引用方差组成模型,将数量性状分解为遗传方差和环境方差,可估计二者对表型的影响。两种方法可应用于同胞对、核心家系或扩展家系,定位数量性状基因座。本文对这两种模型的原理、算法及其进展进行了综述,并给出了常用的统计软件包。 Abstract:In this article, we discussed two model-free methods for detecting genetic linkage for quantitative traits, Haseman-Elston regression approach and variance components approach. The former is a regression approach for detecting linkage based on the squared difference or squared sums in quantitative trait values of sib-pairs and their estimated marker IBD scores. The latter can jointly model covariate effects along with variance components, including genetic component and non-genetic sources of variability. We have outlined the model assumption, the algorithm and the extensions for the both methods.

关 键 词:数量性状  H-E模型  方差组成模型  Key  words  非参数连锁分析  复杂性状疾病  
文章编号:0253-9772(2004)02-0253-04
修稿时间:2002年12月13

Two Approaches of Quantitative-Trait Linkage Analysis
SU Shao-Yong,GU Dong-Feng.Two Approaches of Quantitative-Trait Linkage Analysis[J].Hereditas,2004,26(2):253-256.
Authors:SU Shao-Yong  GU Dong-Feng
Institution:Division of Population Genetics and Prevention, Cardiovascular Institute & Fu Wai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100 037, China. sushaoy@yahoo.com.cn
Abstract:In this article, we discussed two model-free methods for detecting genetic linkage for quantitative traits, Haseman-Elston regression approach and variance components approach. The former is a regression approach for detecting linkage based on the squared difference or squared sums in quantitative trait values of sib-pairs and their estimated marker IBD scores. The latter can jointly model covariate effects along with variance components, including genetic component and non-genetic sources of variability. We have outlined the model assumption, the algorithm and the extensions for the both methods.
Keywords:complex trait disease  nonparametric linkage analysis  quantitative trait  H-E approach  variance components
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