首页> 美国卫生研究院文献>BMC Genomics >Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle
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Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle

机译:使用高密度或中密度单核苷酸多态性基因型面板检测到的拷贝数变异与牛侧翼高密度单核苷酸多态性单倍型插补拷贝数变异的潜力之间的一致性率

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摘要

The first quartile, median, and third quartile for the genomic length, and the number of SNPs per CNV for the CNVs called from the high-density genotypes. The CNVs called from the high-density genotypes are grouped separately based on the degree of overlap of the genomic position of the CNVs called from the high and medium density genotypes. Direct overlap is where is the genomic position of both CNVs were the same, partial overlap is where the genomic positions partially overlapped, and no overlap is where the genomic positions of the CNVs did not overlap
机译:基因组长度的第一个四分位数,中位数和第三个四分位数,以及从高密度基因型调用的CNV的每个CNV的SNP数量。基于高密度和中等密度基因型的CNV的基因组位置重叠程度,分别将高密度基因型的CNV进行分组。直接重叠是两个CNV的基因组位置相同的地方,部分重叠是基因组位置部分重叠的地方,不重叠是CNV的基因组位置不重叠的地方

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