首页> 外文期刊>Human Biology: Official Publication of the Human Biology Council >Allele frequency estimation from ambiguous data: using resampling schema in validating frequency estimates and in selective neutrality testing.
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Allele frequency estimation from ambiguous data: using resampling schema in validating frequency estimates and in selective neutrality testing.

机译:根据模糊数据进行等位基因频率估算:在验证频率估算和选择性中立性测试中使用重采样方案。

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Abstract The development of molecular typing techniques applied to the study of population genetic diversity originates data with increasing precision but at the cost of some ambiguities. As distinct techniques may produce distinct kinds of ambiguities, a crucial issue is to assess the differences between frequency distributions estimated from data produced by alternative techniques for the same sample. To that aim, we developed a resampling scheme that allows evaluating, by statistical means, the significance of the difference between two frequency distributions. The same approach is then shown to be applicable to test selective neutrality when only sample frequencies are known. The use of these original methods is presented here through an application to the genetic study of a Munda human population sample, where three different HLA loci were typed using two different molecular methods (reverse PCR-SSO typing on microbeads arrays based on Luminex technology and PCR-SSP typing), as described in details in the companion article by Riccio et al. [The Austroasiatic Munda population from India and its enigmatic origin: An HLA diversity study. Hum. Biol. 38:405-435 (2011)]. The differences between the frequency estimates of the two typing techniques were found to be smaller than those resulting from sampling. Overall, we show that using a resampling scheme in validating frequency estimates is effective when alternative frequency estimates are available. Moreover, resampling appears to be the unique way to test selective neutrality when only frequency data are available to describe the genetic structure of populations.
机译:摘要用于人口遗传多样性研究的分子分型技术的发展产生了越来越精确的数据,但要付出一些模棱两可的代价。由于不同的技术可能会产生不同类型的歧义,因此关键的问题是评估根据相同样品的替代技术所产生的数据估算出的频率分布之间的差异。为此,我们开发了一种重采样方案,该方案允许通过统计手段评估两个频率分布之间差异的重要性。当仅知道采样频率时,该方法同样适用于测试选择性中立。这些原始方法的使用通过在Munda人群样本的遗传研究中的应用进行介绍,其中使用两种不同的分子方法(在基于Luminex技术和PCR的微珠阵列上进行反向PCR-SSO分型)对三个不同的HLA基因座进行了分型。 -SSP类型),如Riccio等人在随附文章中的详细说明。 [来自印度的奥斯塔蒙达族及其神秘起源:一项HLA多样性研究。哼。生物学38:405-435(2011)]。发现两种打字技术的频率估计之间的差异小于采样产生的差异。总体而言,我们表明,在有备用频率估算可用的情况下,使用重采样方案来验证频率估算是有效的。此外,当只有频率数据可用来描述种群的遗传结构时,重采样似乎是测试选择性中立性的唯一方法。

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