Jewett Ethan M
23andMe, Inc. Sunnyvale, CA., 94086.
bioRxiv. 2024 May 16:2024.05.13.594012. doi: 10.1101/2024.05.13.594012.
In large genotyping datasets, individuals often have thousands of distant cousins with whom they share detectable segments of DNA identically by descent (IBD). The ability to simulate these distant relationships is important for developing and testing methods, carrying out power analyses, and performing population genetic analyses. Because distant relatives are unlikely to share detectable IBD segments by chance, many simulation replicates are needed to sample IBD between any given pair of distant relatives. Exponentially more samples are needed to simulate observable segments of IBD simultaneously among multiple pairs of distant relatives in a single pedigree. Using existing pedigree simulation methods that do not condition on the event that IBD is observed among certain pairs of relatives, the chances of sampling shared IBD patterns that reflect those observed in real data ascertained from large genotyping datasets are vanishingly small, even for pedigrees of modest size. Here, we show how to sample recombination breakpoints on a fixed pedigree while conditioning on the event that specified pairs of individuals share at least one observed segment of IBD. The resulting simulator makes it possible to sample genotypes and IBD segments on pedigrees that reflect those ascertained from biobank scale data.
在大型基因分型数据集中,个体往往有成千上万的远亲,他们通过血缘共享可检测到的相同DNA片段(IBD)。模拟这些远亲关系的能力对于开发和测试方法、进行功效分析以及开展群体遗传学分析至关重要。由于远亲不太可能偶然共享可检测到的IBD片段,因此需要进行许多模拟重复实验,以便在任何给定的一对远亲之间抽样IBD。要在单个谱系中的多对远亲之间同时模拟可观察到的IBD片段,则需要指数级更多的样本。使用现有的谱系模拟方法,这些方法不考虑在某些亲属对中观察到IBD这一事件,那么抽样出反映从大型基因分型数据集中确定的真实数据中所观察到的共享IBD模式的可能性微乎其微,即使对于规模适中的谱系也是如此。在这里,我们展示了如何在固定谱系上对重组断点进行抽样,同时考虑指定个体对共享至少一个观察到的IBD片段这一事件。由此产生的模拟器使得在反映从生物样本库规模数据中确定的谱系上对基因型和IBD片段进行抽样成为可能。