Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data

<p>Abstract</p> <p>Background</p> <p>Structural variations such as copy number variants (CNV) influence the expression of different phenotypic traits. Algorithms to identify CNVs through SNP-array platforms are available. The ability to evaluate well-characterized CNVs...

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Main Authors: Marenne Gaëlle, Real Francisco X, Rothman Nathaniel, Rodríguez-Santiago Benjamin, Pérez-Jurado Luis, Kogevinas Manolis, García-Closas Montse, Silverman Debra T, Chanock Stephen J, Génin Emmanuelle, Malats Núria
Format: Article
Language:English
Published: BMC 2012-07-01
Series:BMC Genomics
Subjects:
Online Access:http://www.biomedcentral.com/1471-2164/13/326
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spelling doaj-803b69ed68a94a81837b7c34bc98a62d2020-11-24T23:08:01ZengBMCBMC Genomics1471-21642012-07-0113132610.1186/1471-2164-13-326Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array dataMarenne GaëlleReal Francisco XRothman NathanielRodríguez-Santiago BenjaminPérez-Jurado LuisKogevinas ManolisGarcía-Closas MontseSilverman Debra TChanock Stephen JGénin EmmanuelleMalats Núria<p>Abstract</p> <p>Background</p> <p>Structural variations such as copy number variants (CNV) influence the expression of different phenotypic traits. Algorithms to identify CNVs through SNP-array platforms are available. The ability to evaluate well-characterized CNVs such as <it>GSTM1</it> (1p13.3) deletion provides an important opportunity to assess their performance.</p> <p>Results</p> <p>773 cases and 759 controls from the SBC/EPICURO Study were genotyped in the <it>GSTM1</it> region using TaqMan, Multiplex Ligation-dependent Probe Amplification (MLPA), and Illumina Infinium 1 M SNP-array platforms. CNV callings provided by TaqMan and MLPA were highly concordant and replicated the association between <it>GSTM1</it> and bladder cancer. This was not the case when CNVs were called using Illumina 1 M data through available algorithms since no deletion was detected across the study samples. In contrast, when the Log R Ratio (LRR) was used as a continuous measure for the 5 probes contained in this locus, we were able to detect their association with bladder cancer using simple regression models or more sophisticated methods such as the ones implemented in the CNVtools package.</p> <p>Conclusions</p> <p>This study highlights an important limitation in the CNV calling from SNP-array data in regions of common aberrations and suggests that there may be added advantage for using LRR as a continuous measure in association tests rather than relying on calling algorithms.</p> http://www.biomedcentral.com/1471-2164/13/326Bladder cancer riskGlutathione <it>S</it>-transferase mu 1 (<it>GSTM1</it>)Copy number variation (CNV)SNP-array
collection DOAJ
language English
format Article
sources DOAJ
author Marenne Gaëlle
Real Francisco X
Rothman Nathaniel
Rodríguez-Santiago Benjamin
Pérez-Jurado Luis
Kogevinas Manolis
García-Closas Montse
Silverman Debra T
Chanock Stephen J
Génin Emmanuelle
Malats Núria
spellingShingle Marenne Gaëlle
Real Francisco X
Rothman Nathaniel
Rodríguez-Santiago Benjamin
Pérez-Jurado Luis
Kogevinas Manolis
García-Closas Montse
Silverman Debra T
Chanock Stephen J
Génin Emmanuelle
Malats Núria
Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data
BMC Genomics
Bladder cancer risk
Glutathione <it>S</it>-transferase mu 1 (<it>GSTM1</it>)
Copy number variation (CNV)
SNP-array
author_facet Marenne Gaëlle
Real Francisco X
Rothman Nathaniel
Rodríguez-Santiago Benjamin
Pérez-Jurado Luis
Kogevinas Manolis
García-Closas Montse
Silverman Debra T
Chanock Stephen J
Génin Emmanuelle
Malats Núria
author_sort Marenne Gaëlle
title Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data
title_short Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data
title_full Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data
title_fullStr Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data
title_full_unstemmed Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data
title_sort genome-wide cnv analysis replicates the association between <it>gstm1</it> deletion and bladder cancer: a support for using continuous measurement from snp-array data
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2012-07-01
description <p>Abstract</p> <p>Background</p> <p>Structural variations such as copy number variants (CNV) influence the expression of different phenotypic traits. Algorithms to identify CNVs through SNP-array platforms are available. The ability to evaluate well-characterized CNVs such as <it>GSTM1</it> (1p13.3) deletion provides an important opportunity to assess their performance.</p> <p>Results</p> <p>773 cases and 759 controls from the SBC/EPICURO Study were genotyped in the <it>GSTM1</it> region using TaqMan, Multiplex Ligation-dependent Probe Amplification (MLPA), and Illumina Infinium 1 M SNP-array platforms. CNV callings provided by TaqMan and MLPA were highly concordant and replicated the association between <it>GSTM1</it> and bladder cancer. This was not the case when CNVs were called using Illumina 1 M data through available algorithms since no deletion was detected across the study samples. In contrast, when the Log R Ratio (LRR) was used as a continuous measure for the 5 probes contained in this locus, we were able to detect their association with bladder cancer using simple regression models or more sophisticated methods such as the ones implemented in the CNVtools package.</p> <p>Conclusions</p> <p>This study highlights an important limitation in the CNV calling from SNP-array data in regions of common aberrations and suggests that there may be added advantage for using LRR as a continuous measure in association tests rather than relying on calling algorithms.</p>
topic Bladder cancer risk
Glutathione <it>S</it>-transferase mu 1 (<it>GSTM1</it>)
Copy number variation (CNV)
SNP-array
url http://www.biomedcentral.com/1471-2164/13/326
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