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首页> 外文期刊>The American Journal of Human Genetics >A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation events.
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A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation events.

机译:通过对重复的单倍体基因组进行基因分型来确定的确定单倍型图谱,在拷贝数变异事件中发现了主要的单倍型偏好。

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摘要

The majority of complete hydatidiform moles (CHMs) harbor duplicated haploid genomes that originate from sperm. This makes CHMs more advantageous than conventional diploid cells for determining haplotypes of SNPs and copy-number variations (CNVs), because all of the genetic variants in a CHM genome are homozygous. Here we report SNP and CNV haplotype structures determined by analysis of 100 CHMs from Japanese subjects via high-density DNA arrays. The obtained haplotype map should be useful as a reference for the haplotype structure of Asian populations. We resolved common CNV regions (merged CNV segments across the examined samples) into CNV events (clusters of CNV segments) on the basis of mutual overlap and found that the haplotype backgrounds of different CNV events within the same CNV region were predominantly similar, perhaps because of inherent structural instability.
机译:大多数完整的葡萄胎(CHM)都有重复的源自精子的单倍体基因组。这使得CHM在确定SNP的单倍型和拷贝数变异(CNV)方面​​比常规二倍体细胞更具优势,因为CHM基因组中的所有遗传变异都是纯合的。在这里,我们报告了SNP和CNV单倍型结构,该结构是通过对来自日本受试者的100个CHM通过高密度DNA阵列进行分析而确定的。所获得的单倍型图谱应作为亚洲人群单倍型结构的参考。我们在相互重叠的基础上将常见的CNV区域(合并的CNV片段跨检查的样本)分解为CNV事件(CNV片段的簇),并发现同一CNV区域内不同CNV事件的单倍型背景主要相似。固有的结构不稳定性。

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