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Detecting and Removing Ascertainment Bias in Microsatellites from the HGDP-CEPH Panel

机译:从HGDP-CEPH面板中检测和消除微卫星中的确定性偏差

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摘要

Although ascertainment bias in single nucleotide polymorphisms is a well-known problem, it is generally accepted that microsatellites have mutation rates too high for bias to be a concern. Here, we analyze in detail the large set of microsatellites typed for the Human Genetic Diversity Panel (HGDP)-CEPH panel. We develop a novel framework based on rarefaction to compare heterozygosity across markers with different mutation rates. We find that, whereas di- and tri-nucleotides show similar patterns of within- and between-population heterozygosity, tetra-nucleotides are inconsistent with the other two motifs. In addition, di- and tri-nucleotides are consistent with 16 unbiased tetra-nucleotide markers, whereas the HPGP-CEPH tetra-nucleotides are significantly different. This discrepancy is due to the HGDP-CEPH tetra-nucleotides being too homogeneous across Eurasia, even after their slower mutation rate is taken into account by rarefying the other markers. The most likely explanation for this pattern is ascertainment bias. We strongly advocate the exclusion of tetra-nucleotides from future population genetics analysis of this dataset, and we argue that other microsatellite datasets should be investigated for the presence of bias using the approach outlined in this article.
机译:尽管确定单核苷酸多态性的偏倚是一个众所周知的问题,但人们普遍认为微卫星的突变率太高而使偏倚成为一个问题。在这里,我们详细分析了为人类遗传多样性面板(HGDP)-CEPH面板键入的大量微卫星。我们开发了一种基于稀疏性的新颖框架,以比较具有不同突变率的标记之间的杂合性。我们发现,虽然二核苷酸和三核苷酸显示出种群内和种群间杂合性的相似模式,但四核苷酸与其他两个基序不一致。此外,二核苷酸和三核苷酸与16个无偏四核苷酸标记是一致的,而HPGP-CEPH四核苷酸则有显着差异。这种差异是由于HGDP-CEPH四核苷酸在整个欧亚大陆上过于同质,即使在通过消除其他标记来考虑其较慢的突变率之后也是如此。这种模式最可能的解释是确定偏差。我们强烈主张从该数据集的未来人群遗传学分析中排除四核苷酸,并认为应使用本文概述的方法调查其他微卫星数据集是否存在偏倚。

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