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Joint Estimates of Heterozygosity and Runs of Homozygosity for Modern and Ancient Samples

机译:现代和古代样本的杂合度和纯合度联合估计

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摘要

Both the total amount and the distribution of heterozygous sites within individual genomes are informative about the genetic diversity of the population they belong to. Detecting true heterozygous sites in ancient genomes is complicated by the generally limited coverage achieved and the presence of post-mortem damage inflating sequencing errors. Additionally, large runs of homozygosity found in the genomes of particularly inbred individuals and of domestic animals can skew estimates of genome-wide heterozygosity rates. Current computational tools aimed at estimating runs of homozygosity and genome-wide heterozygosity levels are generally sensitive to such limitations. Here, we introduce ROHan, a probabilistic method which substantially improves the estimate of heterozygosity rates both genome-wide and for genomic local windows. It combines a local Bayesian model and a Hidden Markov Model at the genome-wide level and can work both on modern and ancient samples. We show that our algorithm outperforms currently available methods for predicting heterozygosity rates for ancient samples. Specifically, ROHan can delineate large runs of homozygosity (at megabase scales) and produce a reliable confidence interval for the genome-wide rate of heterozygosity outside of such regions from modern genomes with a depth of coverage as low as 5–6× and down to 7–8× for ancient samples showing moderate DNA damage. We apply ROHan to a series of modern and ancient genomes previously published and revise available estimates of heterozygosity for humans, chimpanzees and horses.
机译:单个基因组中杂合位点的总量和分布都可为它们所属种群的遗传多样性提供信息。由于通常有限的覆盖范围和事后破坏的存在会加剧测序错误,因此检测古代基因组中真正的杂合位点变得很复杂。此外,在特别近交个体和家畜的基因组中发现的大量纯合子可能会使全基因组杂合率的估计值产生偏差。当前旨在估计纯合和全基因组杂合水平运行的计算工具通常对此类限制敏感。在这里,我们介绍了ROHan,这是一种概率方法,可显着提高全基因组范围和基因组局部窗口的杂合率估计。它在全基因组水平上结合了本地贝叶斯模型和隐马尔可夫模型,并且可以在现代和古代样本中使用。我们表明,我们的算法优于目前用于预测古代样本杂合率的方法。特别是,ROHan可以描绘出大量纯合子(以兆碱基为单位),并为现代基因组中此类区域之外的全基因组杂合率产生了可靠的置信区间,覆盖范围低至5-6倍,低至古代样本的DNA损伤程度为7–8倍。我们将ROHan应用到先前发布的一系列现代和古代基因组中,并修改了人类,黑猩猩和马的杂合性的可用估计。

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