Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA.
Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Genetics. 2024 Sep 4;228(1). doi: 10.1093/genetics/iyae098.
Most gene expression and alternative splicing quantitative trait loci (eQTL/sQTL) studies have been biased toward European ancestry individuals. Here, we performed eQTL and sQTL analyses using TOPMed whole-genome sequencing-derived genotype data and RNA-sequencing data from stored peripheral blood mononuclear cells in 1,012 African American participants from the Jackson Heart Study (JHS). At a false discovery rate of 5%, we identified 17,630 unique eQTL credible sets covering 16,538 unique genes; and 24,525 unique sQTL credible sets covering 9,605 unique genes, with lead QTL at P < 5e-8. About 24% of independent eQTLs and independent sQTLs with a minor allele frequency > 1% in JHS were rare (minor allele frequency < 0.1%), and therefore unlikely to be detected, in European ancestry individuals. Finally, we created an open database, which is freely available online, allowing fast query and bulk download of our QTL results.
大多数基因表达和选择性剪接数量性状基因座(eQTL/sQTL)研究都偏向于欧洲血统个体。在这里,我们使用来自存储的外周血单核细胞的全基因组测序衍生基因型数据和 RNA 测序数据,对来自杰克逊心脏研究(JHS)的 1012 名非裔美国人参与者进行了 eQTL 和 sQTL 分析。在错误发现率为 5%的情况下,我们确定了 17,630 个独特的 eQTL 可信集,涵盖了 16,538 个独特的基因;以及 24,525 个独特的 sQTL 可信集,涵盖了 9,605 个独特的基因,其中主要 QTL 的 P 值小于 5e-8。在 JHS 中,具有频率 > 1%的独立 eQTL 和独立 sQTL 中约有 24%是罕见的(次要等位基因频率 < 0.1%),因此在欧洲血统个体中不太可能被检测到。最后,我们创建了一个开放的数据库,可在线免费访问,允许快速查询和批量下载我们的 QTL 结果。