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A cross-platform analysis of 14177 expression quantitative trait loci derived from lymphoblastoid cell lines

机译:跨平台分析来自成淋巴细胞样细胞系的14177个表达数量性状基因座

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摘要

Gene expression levels can be an important link DNA between variation and phenotypic manifestations. Our previous map of global gene expression, based on ∼400K single nucleotide polymorphisms (SNPs) and 50K transcripts in 400 sib pairs from the MRCA family panel, has been widely used to interpret the results of genome-wide association studies (GWASs). Here, we more than double the size of our initial data set with expression data on 550 additional individuals from the MRCE family panel using the Illumina whole-genome expression array. We have used new statistical methods for dimension reduction to account for nongenetic effects in estimates of expression levels, and we have also included SNPs imputed from the 1000 Genomes Project. Our methods reduced false-discovery rates and increased the number of expression quantitative trait loci (eQTLs) mapped either locally or at a distance (i.e., in cis or trans) from 1534 in the MRCA data set to 4452 (with <5% FDR). Imputation of 1000 Genomes SNPs further increased the number of eQTLs to 7302. Using the same methods and imputed SNPs in the newly acquired MRCE data set, we identified eQTLs for 9000 genes. The combined results identify strong local and distant effects for transcripts from 14,177 genes. Our eQTL database based on these results is freely available to help define the function of disease-associated variants.
机译:基因表达水平可能是变异与表型表现之间重要的联系DNA。我们以前的全球基因表达图谱是基于MRCA家族中400个同胞对中的〜400K单核苷酸多态性(SNP)和50K转录本,已被广泛用于解释全基因组关联研究(GWAS)的结果。在这里,我们使用Illumina全基因组表达阵列将原始数据集的大小增加了一倍,其中有来自MRCE家族的550位其他个体的表达数据。我们使用了新的统计方法来进行维数缩减,以在表达水平的估计中考虑非遗传效应,并且还包括了从1000个基因组计划中推算出的SNP。我们的方法降低了错误发现率,并增加了从MRCA数据集中的1534到4452(具有小于5%FDR)的局部或距离(即顺式或反式)映射的表达定量特征位点(eQTL)数量。估算1000个基因组SNP进一步将eQTL的数量增加到7302。使用相同的方法并在新获得的MRCE数据集中估算SNP,我们鉴定了9000个基因的eQTL。合并结果确定了来自14,177个基因的转录本的强局部和远距离作用。我们免费提供基于这些结果的eQTL数据库,以帮助定义疾病相关变体的功能。

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