Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.

Following the widespread use of genome-wide association studies (GWAS), focus is turning towards identification of causal variants rather than simply genetic markers of diseases and traits. As a step towards a high-throughput method to identify genome-wide, non-coding, functional regulatory variants...

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Main Authors: Andrew J P Smith, Philip Howard, Sonia Shah, Per Eriksson, Stefan Stender, Claudia Giambartolomei, Lasse Folkersen, Anne Tybjærg-Hansen, Meena Kumari, Jutta Palmen, Aroon D Hingorani, Philippa J Talmud, Steve E Humphries
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1002908&type=printable
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author Andrew J P Smith
Philip Howard
Sonia Shah
Per Eriksson
Stefan Stender
Claudia Giambartolomei
Lasse Folkersen
Anne Tybjærg-Hansen
Meena Kumari
Jutta Palmen
Aroon D Hingorani
Philippa J Talmud
Steve E Humphries
author_facet Andrew J P Smith
Philip Howard
Sonia Shah
Per Eriksson
Stefan Stender
Claudia Giambartolomei
Lasse Folkersen
Anne Tybjærg-Hansen
Meena Kumari
Jutta Palmen
Aroon D Hingorani
Philippa J Talmud
Steve E Humphries
author_sort Andrew J P Smith
collection DOAJ
description Following the widespread use of genome-wide association studies (GWAS), focus is turning towards identification of causal variants rather than simply genetic markers of diseases and traits. As a step towards a high-throughput method to identify genome-wide, non-coding, functional regulatory variants, we describe the technique of allele-specific FAIRE, utilising large-scale genotyping technology (FAIRE-gen) to determine allelic effects on chromatin accessibility and regulatory potential. FAIRE-gen was explored using lymphoblastoid cells and the 50,000 SNP Illumina CVD BeadChip. The technique identified an allele-specific regulatory polymorphism within NR1H3 (coding for LXR-α), rs7120118, coinciding with a previously GWAS-identified SNP for HDL-C levels. This finding was confirmed using FAIRE-gen with the 200,000 SNP Illumina Metabochip and verified with the established method of TaqMan allelic discrimination. Examination of this SNP in two prospective Caucasian cohorts comprising 15,000 individuals confirmed the association with HDL-C levels (combined beta = 0.016; p = 0.0006), and analysis of gene expression identified an allelic association with LXR-α expression in heart tissue. Using increasingly comprehensive genotyping chips and distinct tissues for examination, FAIRE-gen has the potential to aid the identification of many causal SNPs associated with disease from GWAS.
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spelling doaj-art-5e4c591f9f444fc788fb8731f0d5bd0c2025-08-20T02:05:37ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042012-01-0188e100290810.1371/journal.pgen.1002908Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.Andrew J P SmithPhilip HowardSonia ShahPer ErikssonStefan StenderClaudia GiambartolomeiLasse FolkersenAnne Tybjærg-HansenMeena KumariJutta PalmenAroon D HingoraniPhilippa J TalmudSteve E HumphriesFollowing the widespread use of genome-wide association studies (GWAS), focus is turning towards identification of causal variants rather than simply genetic markers of diseases and traits. As a step towards a high-throughput method to identify genome-wide, non-coding, functional regulatory variants, we describe the technique of allele-specific FAIRE, utilising large-scale genotyping technology (FAIRE-gen) to determine allelic effects on chromatin accessibility and regulatory potential. FAIRE-gen was explored using lymphoblastoid cells and the 50,000 SNP Illumina CVD BeadChip. The technique identified an allele-specific regulatory polymorphism within NR1H3 (coding for LXR-α), rs7120118, coinciding with a previously GWAS-identified SNP for HDL-C levels. This finding was confirmed using FAIRE-gen with the 200,000 SNP Illumina Metabochip and verified with the established method of TaqMan allelic discrimination. Examination of this SNP in two prospective Caucasian cohorts comprising 15,000 individuals confirmed the association with HDL-C levels (combined beta = 0.016; p = 0.0006), and analysis of gene expression identified an allelic association with LXR-α expression in heart tissue. Using increasingly comprehensive genotyping chips and distinct tissues for examination, FAIRE-gen has the potential to aid the identification of many causal SNPs associated with disease from GWAS.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1002908&type=printable
spellingShingle Andrew J P Smith
Philip Howard
Sonia Shah
Per Eriksson
Stefan Stender
Claudia Giambartolomei
Lasse Folkersen
Anne Tybjærg-Hansen
Meena Kumari
Jutta Palmen
Aroon D Hingorani
Philippa J Talmud
Steve E Humphries
Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
PLoS Genetics
title Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
title_full Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
title_fullStr Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
title_full_unstemmed Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
title_short Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
title_sort use of allele specific faire to determine functional regulatory polymorphism using large scale genotyping arrays
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1002908&type=printable
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