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A comprehensive profile of DNA copy number variations in a Korean population: identification of copy number invariant regions among Koreans

机译:韩国人口中DNA拷贝数变异的全面概况:确定韩国人中拷贝数不变区域

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To examine copy number variations among the Korean population, we compared individual genomes with the Korean reference genome assembly using the publicly available Korean HapMap SNP 50 k chip data from 90 individuals. Korean individuals exhibited 123 copy number variation regions (CNVRs) covering 27.2 mb, equivalent to 1.0% of the genome in the copy number variation (CNV) analysis using the combined criteria of P value (P n = 643) were detected in larger proportions (5.0%) of the genome covering 135.1 mb even by more stringent criteria (P < 0.001 and SD ≥ 0.25), reflecting ethnic diversity of structural variations between Korean and other populations. Some CNVRs were validated by the quantitative multiplex PCR of short fluorescent fragment (QMPSF) method, and then copy number invariant regions were detected among the study subjects. These copy number invariant regions would be used as good internal controls for further CNV studies. Lastly, we demonstrated that the CNV information could stratify even a single ethnic population with a proper reference genome assembly from multiple heterogeneous populations.
机译:为了检查韩国人群之间的拷贝数变异,我们使用来自90个个体的可公开获得的韩国HapMap SNP 50 k芯片数据,将单个基因组与韩国参考基因组进行了比较。韩国人的123个拷贝数变异区(CNVR)覆盖27.2 mb,相当于使用P值组合标准(P n = 643)在拷贝数变异(CNV)分析中占基因组的1.0%。即使按照更严格的标准(P <0.001和SD≥0.25),基因组的比例(5.0%)也能覆盖135.1 mb,反映出韩国人与其他人群之间结构变异的种族多样性。通过短荧光片段定量多重PCR(QMPSF)方法对一些CNVR进行了验证,然后在研究对象中检测出拷贝数不变区域。这些拷贝数不变区域将被用作进一步CNV研究的良好内部对照。最后,我们证明了CNV信息甚至可以将来自多个异质种群的适当参考基因组装配成一个种族种群。

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