Zhao J, Li W, Xiong M
Human Genetics Center, University of Texas-Houston, Houston, Texas, USA.
Genet Epidemiol. 2001;21 Suppl 1:S655-9. doi: 10.1002/gepi.2001.21.s1.s655.
Despite successes in mapping and cloning genes involved in rare Mendelian diseases, genetic dissection of quantitative traits into single Mendelian factors still remains a challenging task. As the dense map of single nucleotide polymorphism (SNP) markers becomes available in the near future, linkage disequilibrium (LD) mapping will become one of major tools for mapping and identifying quantitative trait loci (QTL). In this report, we present a population-based linkage disequilibrium mapping of QTL. This method unifies the analysis of mapping QTL in humans and in model organisms and can be used for randomly sampled individuals. The proposed method is applied to search for polymorphism sites within the candidate genes 2 and 6, which influence quantitative traits Q1 and Q2 or Q5, in a simulated data set in an isolated population.
尽管在绘制和克隆与罕见孟德尔疾病相关的基因方面取得了成功,但将数量性状解析为单个孟德尔因子仍然是一项具有挑战性的任务。随着单核苷酸多态性(SNP)标记的密集图谱在不久的将来可用,连锁不平衡(LD)图谱将成为绘制和识别数量性状基因座(QTL)的主要工具之一。在本报告中,我们展示了一种基于群体的QTL连锁不平衡图谱。该方法统一了人类和模式生物中QTL图谱分析,可用于随机抽样个体。所提出的方法应用于在一个隔离群体的模拟数据集中搜索候选基因2和6内的多态性位点,这些基因影响数量性状Q1和Q2或Q5。