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Monte Carlo estimation of identity by descent in populations.

机译:蒙特卡洛(Monte Carlo)通过血统在人群中的身份估计

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摘要

Genetic similarity between organisms arises from segments of shared genome, which are said to be identical by descent (IBD). Modeling IBD in pedigrees forms the basis of classical linkage analysis and has been a fruitful method for inferring trait locations. We examine methods for modeling IBD in more general settings where relationships among subjects are not known completely. A natural approach is to use a hidden Markov model (HMM) based on a transition model for IBD along the chromosome, but the number of possible IBD states for more than a few individuals makes makes standard HMM calculations infeasible. We describe two broad approaches to sampling from this model. First, we decompose the group IBD model into a series of pairwise approximations which can be sampled efficiently. This decomposition permits other modifications to the model so that it can be used with unphased genotypes or incomplete pedigree information. Second, we implement a particle Gibbs sampling algorithm for the HMM, which is computationally intensive but targets the correct model. Both methods are compared against exact HMM sampling. The particle Gibbs method more accurately captures the true model distribution at the expense of increased computation time.
机译:生物体之间的遗传相似性来自共享基因组的片段,据传其血统相同(IBD)。在谱系中对IBD建模是经典连锁分析的基础,并且已经成为推断性状位置的有效方法。我们研究了在更一般的环境中对IBD建模的方法,在这些环境中,对象之间的关系尚不完全清楚。一种自然的方法是使用基于沿染色体的IBD过渡模型的隐马尔可夫模型(HMM),但是对于多个个体而言,可能的IBD状态数量过多使得标准HMM计算不可行。我们描述了两种从该模型进行抽样的广泛方法。首先,我们将IBD组模型分解为可以有效采样的一系列成对近似值。这种分解允许对模型进行其他修改,以便可以与无阶段基因型或不完整的谱系信息一起使用。其次,我们为HMM实现了一种粒子Gibbs采样算法,该算法计算量大,但针对的是正确的模型。将这两种方法与精确的HMM采样进行比较。粒子Gibbs方法以增加的计算时间为代价,更准确地捕获了真实的模型分布。

著录项

  • 作者

    Glazner, Christopher.;

  • 作者单位

    University of Washington.;

  • 授予单位 University of Washington.;
  • 学科 Statistics.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 92 p.
  • 总页数 92
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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