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A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines

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 th...

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Autores principales: Liang, Liming, Morar, Nilesh, Dixon, Anna L., Lathrop, G. Mark, Abecasis, Goncalo R., Moffatt, Miriam F., Cookson, William O.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613588/
https://www.ncbi.nlm.nih.gov/pubmed/23345460
http://dx.doi.org/10.1101/gr.142521.112
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author Liang, Liming
Morar, Nilesh
Dixon, Anna L.
Lathrop, G. Mark
Abecasis, Goncalo R.
Moffatt, Miriam F.
Cookson, William O.C.
author_facet Liang, Liming
Morar, Nilesh
Dixon, Anna L.
Lathrop, G. Mark
Abecasis, Goncalo R.
Moffatt, Miriam F.
Cookson, William O.C.
author_sort Liang, Liming
collection PubMed
description 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.
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spelling pubmed-36135882013-04-03 A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines Liang, Liming Morar, Nilesh Dixon, Anna L. Lathrop, G. Mark Abecasis, Goncalo R. Moffatt, Miriam F. Cookson, William O.C. Genome Res Resource 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. Cold Spring Harbor Laboratory Press 2013-04 /pmc/articles/PMC3613588/ /pubmed/23345460 http://dx.doi.org/10.1101/gr.142521.112 Text en © 2013, Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Resource
Liang, Liming
Morar, Nilesh
Dixon, Anna L.
Lathrop, G. Mark
Abecasis, Goncalo R.
Moffatt, Miriam F.
Cookson, William O.C.
A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
title A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
title_full A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
title_fullStr A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
title_full_unstemmed A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
title_short A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
title_sort cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613588/
https://www.ncbi.nlm.nih.gov/pubmed/23345460
http://dx.doi.org/10.1101/gr.142521.112
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