The expression Quantitative Traits Locus (eQTL) is a genetic polymorphism associated with changes in gene expression levels. They have been successfully used to pioritize the target genes of the variants associated with complex traits and diseases (GWAS variants). Existing eQTLs databases collect only a small portion of the available datasets. We planned to build the largest publically available catalog of eQTLs, coupled with a browser, to optimize and simplify their interrogation. We collected and manually curated 51 eQTL public studies ranging from 2007 to date, corresponding to more than 94 tissues/cells/conditions and 15 human populations for a total of 275,727 cis-eQTLs and 33,241 genes with at least one cis-eQTL (cis-eGenes). We found that for 93% of the known protein-coding genes were eGenes, 22% of them intersecting (r2≥0.8) with the NHGRI-EBI GWAS Catalog and 26% of whom considered as druggable. Furthermore, for those GWAS variants for which at least an eGene was known, we found that the NHGRI-EBI GWAS Catalog proposed at least one of the same genes as candidate target only for the 70% of the times. Our eQTL-Catalog can be used as a reference to measure the degree of novelty for future eQTLs studies; it is provided within a platform with the web-browser LinDA (http://linda.irgb.cnr.it) implemented with other types of quantitative traits (i.e. epigenetic, proteomic) to better dissect the pleiotropy of the GWAS variants.
The EQTLs Catalog and LinDA browser: a platform for determining the effects on transcription of GWAS variants / Onano, Stefano. - (2019).
The EQTLs Catalog and LinDA browser: a platform for determining the effects on transcription of GWAS variants
Onano, Stefano
2019-01-01
Abstract
The expression Quantitative Traits Locus (eQTL) is a genetic polymorphism associated with changes in gene expression levels. They have been successfully used to pioritize the target genes of the variants associated with complex traits and diseases (GWAS variants). Existing eQTLs databases collect only a small portion of the available datasets. We planned to build the largest publically available catalog of eQTLs, coupled with a browser, to optimize and simplify their interrogation. We collected and manually curated 51 eQTL public studies ranging from 2007 to date, corresponding to more than 94 tissues/cells/conditions and 15 human populations for a total of 275,727 cis-eQTLs and 33,241 genes with at least one cis-eQTL (cis-eGenes). We found that for 93% of the known protein-coding genes were eGenes, 22% of them intersecting (r2≥0.8) with the NHGRI-EBI GWAS Catalog and 26% of whom considered as druggable. Furthermore, for those GWAS variants for which at least an eGene was known, we found that the NHGRI-EBI GWAS Catalog proposed at least one of the same genes as candidate target only for the 70% of the times. Our eQTL-Catalog can be used as a reference to measure the degree of novelty for future eQTLs studies; it is provided within a platform with the web-browser LinDA (http://linda.irgb.cnr.it) implemented with other types of quantitative traits (i.e. epigenetic, proteomic) to better dissect the pleiotropy of the GWAS variants.File | Dimensione | Formato | |
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