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Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex Traits

机译:利用DNA-甲基化定量 - 特质锁定表征甲基MENIC变异,基因表达和复杂性状之间的关系

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摘要

Characterizing the complex relationship between genetic, epigenetic, and transcriptomic variation has the potential to increase understanding about the mechanisms underpinning health and disease phenotypes. We undertook a comprehensive analysis of common genetic variation on DNA methylation (DNAm) by using the Illumina EPIC array to profile samples from the UK Household Longitudinal study. We identified 12,689,548 significant DNA methylation quantitative trait loci (mQTL) associations (p 60 human traits by usingsummary-data-basedMendelianrandomization (SMR) to identify 1,662 pleiotropic associations between 36 complex traits and 1,246 DNAm sites. We also use SMR to characterize the relationship between DNAm and gene expression and thereby identify 6,798 pleiotropic associations between 5,420 DNAm sites and the transcription of 1,702 genes. Our mQTL database and SMR results are available via a searchable online database as a resource to the research community.
机译:表征遗传,表观遗传和转录组变异之间的复杂关系有可能提高了解保健和疾病表型的机制。 我们通过使用Illumina Epic阵列对来自英国家庭纵向研究的样本来进行综合分析DNA甲基化(DNAM)的常见遗传变异。 我们鉴定了12,689,548个重要的DNA甲基化定量性状点基因座(MQTL)关联(P60通过Usingsummary-Data-Data-BasianRandomization(SMR),以鉴定36个复杂性特征和1,246个DNAM位点之间的1,662个抗性关联。我们也使用SMR来表征关系之间的关系 DNAM和基因表达,从而鉴定了5,420 dnam位点的6,798个抗性关联和1,702个基因的转录。我们的MQTL数据库和SMR结果可通过可搜索的在线数据库作为研究社区的资源。

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