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一种改进中东和非洲之角代表性不足人群的群体遗传学分析及参考偏倚的泛基因组方法。

A Pangenomic Approach to Improve Population Genetics Analysis and Reference Bias in Underrepresented Middle Eastern and Horn of Africa Populations.

作者信息

Oliva Adrien, Foare Rachel, Campbell Peter, Twine Natalie A, Bauer Denis C, Johar Angad Singh

机构信息

Australian e-Health Research Centre, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Melbourne 3169, Australia.

Life Sciences and Health Graduate School, Université Paris-Saclay, 3 Rue Joliot Curie, 91190 Gif-sur-Yvette, France.

出版信息

Biomolecules. 2025 Apr 15;15(4):582. doi: 10.3390/biom15040582.

Abstract

Genomics plays a crucial role in addressing health disparities, yet most studies rely on the hg38 linear reference genome, limiting the potential of pangenomic approaches, particularly for underrepresented populations. In this study, we focus on characterising East African populations, particularly Somalis, by constructing a variation graph using Mozabites from the Human Genome Diversity Project (HGDP) given their ancestral affinity with Somalis. We evaluated the effectiveness of this graph-based reference in estimating effective population sizes () in Bedouins compared to the hg38 reference and examined its impact on allele frequencies and genome-wide association studies (GWAS). Applying a coalescent model to the graph-based reference produced a estimate of approximately 17 for the Bedouin population, which was significantly lower than the estimate from the hg38 reference (approximately 79,000). Only the graph-based estimate fell within the 95% confidence interval in simulations, indicating improved accuracy. Moreover, graph variants exhibited significantly lower allele frequencies (-value < 2.2 × 10), suggesting potential effects on the interpretation and power of GWAS. Notably, GWAS variants specific to Bedouins derived from the graph showed lower frequencies ( = 0.023) than those obtained from the linear reference. These findings suggest that a pangenomic approach, informed by populations with ancestral affinities such as the Mozabites, provides more accurate estimates of and allele frequencies. This highlights the importance of pangenomic strategies to better capture genetic diversity in underrepresented populations, a critical step towards improving population genetics studies, personalised medicine, and equitable healthcare.

摘要

基因组学在解决健康差异方面发挥着关键作用,但大多数研究依赖于hg38线性参考基因组,限制了泛基因组方法的潜力,特别是对于代表性不足的人群。在本研究中,我们专注于对东非人群,特别是索马里人群进行特征描述,通过利用人类基因组多样性计划(HGDP)中的莫扎比特人构建变异图,因为他们与索马里人有亲缘关系。我们评估了这种基于图的参考在估计贝都因人有效种群大小()方面相对于hg38参考的有效性,并研究了其对等位基因频率和全基因组关联研究(GWAS)的影响。将合并模型应用于基于图的参考得出贝都因人群的估计值约为17,这显著低于hg38参考的估计值(约79,000)。在模拟中,只有基于图的估计值落在95%置信区间内,表明准确性有所提高。此外,图变异显示出显著更低的等位基因频率(-值<2.2×10),表明对GWAS的解释和效能可能有影响。值得注意的是,从图中得出的贝都因人特有的GWAS变异显示出比从线性参考中获得的变异更低的频率(=0.023)。这些发现表明,一种由具有亲缘关系的人群如莫扎比特人提供信息的泛基因组方法,能提供更准确的有效种群大小和等位基因频率估计值。这突出了泛基因组策略对于更好地捕捉代表性不足人群中的遗传多样性的重要性,这是改善群体遗传学研究、个性化医疗和公平医疗保健的关键一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c03f/12025191/a559f6169041/biomolecules-15-00582-g001.jpg

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