Department of Biostatistics, University of Washington, Seattle, Washington, 98195, USA.
Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington, 98195, USA.
G3 (Bethesda). 2023 Sep 30;13(10). doi: 10.1093/g3journal/jkad165.
The effective size of a population (Ne) in the recent past can be estimated through analysis of identity-by-descent (IBD) segments. Several methods have been developed for estimating Ne from autosomal IBD segments, but no such effort has been made with X chromosome IBD segments. In this work, we propose a method to estimate the X chromosome effective population size from X chromosome IBD segments. We show how to use the estimated autosome Ne and X chromosome Ne to estimate the female and male effective population sizes. We demonstrate the accuracy of our autosome and X chromosome Ne estimation with simulated data. We find that the estimated female and male effective population sizes generally reflect the simulated sex-specific effective population sizes across the past 100 generations but that short-term differences between the estimated sex-specific Ne across tens of generations may not reliably indicate true sex-specific differences. We analyzed the effective size of populations represented by samples of sequenced UK White British and UK Indian individuals from the UK Biobank.
近期人口的有效大小(Ne)可以通过分析同源片段(IBD)来估计。已经开发了几种从常染色体 IBD 片段估计 Ne 的方法,但尚未对 X 染色体 IBD 片段进行此类研究。在这项工作中,我们提出了一种从 X 染色体 IBD 片段估计 X 染色体有效种群大小的方法。我们展示了如何使用估计的常染色体 Ne 和 X 染色体 Ne 来估计女性和男性有效种群大小。我们使用模拟数据验证了我们的常染色体和 X 染色体 Ne 估计的准确性。我们发现,估计的女性和男性有效种群大小通常反映了过去 100 代中模拟的特定性别的有效种群大小,但在数十代中估计的特定性别的 Ne 之间的短期差异可能无法可靠地指示真实的特定性别的差异。我们分析了来自英国生物银行的 UK 白人和 UK 印度个体样本所代表的群体的有效大小。