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Haplotype inference for population data with genotyping errors

机译:具有基因分型错误的总体数据的单倍型推断

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Inference of haplotypes is important in genetic epidemiology studies. However, all large genotype data sets have errors due to the use of inexpensive genotyping machines that are fallible and shortcomings in genotyping scoring softwares, which can have an enormous impact on haplotype inference. In this article, we propose two novel strategies to reduce the impact induced by genotyping errors in haplotype inference. The first method makes use of double sampling. For each individual, the "GenoSpectrum" that consists of all possible genotypes and their corresponding likelihoods are computed. The second method is a genotype clustering algorithm based on multi-genotyping data, which also assigns a "GenoSpectrum" for each individual. We then describe two hybrid EM algorithms (called DS-EM and MG-EM) that perform haplotype inference based on "GenoSpectrum" of each individual obtained by double sampling and multi-genotyping data. Both simulated data sets and a quasi real-data set demonstrate that our proposed methods perform well in different situations and outperform the conventional EM algorithm and the HMM algorithm proposed by Sun, Greenwood, and Neal (2007, Genetic Epidemiology 31, 937-948) when the genotype data sets have errors.
机译:单倍型的推断在遗传流行病学研究中很重要。然而,由于使用廉价的基因分型机容易出错,所有大型基因型数据集都有错误,并且基因分型评分软件存在缺陷,这可能对单倍型推断产生巨大影响。在本文中,我们提出了两种新颖的策略来减少单倍型推断中基因分型错误所引起的影响。第一种方法利用了双重采样。对于每个个体,计算由所有可能的基因型组成的“ GenoSpectrum”及其对应的可能性。第二种方法是基于多基因型数据的基因型聚类算法,该算法还为每个个体分配一个“ GenoSpectrum”。然后,我们描述了两种混合EM算法(称为DS-EM和MG-EM),它们基于通过两次采样和多基因分型数据获得的每个个体的“ GenoSpectrum”执行单元型推断。仿真数据集和准真实数据集均表明,我们提出的方法在不同情况下表现良好,并且优于Sun,Greenwood和Neal提出的常规EM算法和HMM算法(2007年,遗传流行病学31,937-948)当基因型数据集有错误时。

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