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NullHap – a versatile application to estimate haplotype frequencies from unphased genotypes in the presence of null alleles

机译:NullHap –在存在无效等位基因的情况下,可以根据未定相基因型估算单倍型频率的通用应用程序

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Background Laboratory techniques used to determine haplotypes are often too expensive for large-scale studies and lack of phase information is commonly overcome using likelihood-based calculations. Whereas a number of programs are available for that purpose, none of them can handle loci with both multiple and null alleles. Results Here we present a description of a modified Expectation – Maximization algorithm as well as its implementation (NullHap) which allow to effectively overcome these limitations. As an example of application we used Nullhap to reanalyze published data on distribution of KIR genotypes in Polish psoriasis patients and controls showing that the KIR2DS4/1D locus may be a marker of KIR2DS1 haplotypes with different effects on disease susceptibility. Conclusion The developed application can estimate haplotype frequencies for every type of polymorphism and can effectively be used in genetic research as illustrated by a novel finding regarding the genetic susceptibility to psoriasis.
机译:背景技术用于确定单倍型的实验室技术通常对于大规模研究而言过于昂贵,并且通常使用基于似然性的计算来克服相位信息的缺乏。尽管有许多程序可用于该目的,但它们均不能处理具有多个等位基因和无效等位基因的基因座。结果在这里,我们介绍了一种改进的Expectation – Maximization算法及其实现(NullHap)的描述,该算法可有效克服这些限制。作为应用示例,我们使用Nullhap重新分析了波兰银屑病患者和对照中KIR基因型分布的公开数据,显示KIR2DS4 / 1D基因座可能是KIR2DS1单倍型的标志物,对疾病易感性的影响不同。结论所开发的应用程序可以估算每种多态性的单倍型频率,并且可以有效地用于遗传学研究,如有关牛皮癣的遗传易感性的新发现所示。

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