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A rapid and simple method to isolate and characterize highly polymorphic markers from the centromeric regions of the human chromosomes

机译:从人类染色体着丝粒区域分离和鉴定高度多态性标记的快速简便方法

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摘要

Using oligonucleotide primers complementary to the 3′ ends of either the Alu or the L1Hs consensus sequences In conjunction with a primer complementary to alpha satellite subsets specific to different human chromosomes, It was possible to detect and characterize polymorphisms originating from the microsatellltes which are often present downstream these repetitive elements. The methodology does not require cloning, sequencing or synthesis of specific primers. Centromeric location was confirmed by linkage analysis, In situ hybridization and sequencing. The method Is proposed for the generation of polymorphic markers from all centromeric regions.
机译:使用与Alu或L1Hs共有序列的3'末端互补的寡核苷酸引物,与与不同人类染色体特异的α卫星子集互补的引物,可以检测和鉴定源自经常存在的微卫星的多态性这些重复元素的下游。该方法不需要特定引物的克隆,测序或合成。通过连锁分析,原位杂交和测序确定着丝粒的位置。提出了从所有着丝粒区域产生多态性标记的方法。

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