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Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples

The discordance in results of independent genome-wide association studies (GWAS) indicates the potential for Type I and Type II errors. We assessed the repeatibility of current Affymetrix technologies that support GWAS. Reasonable reproducibility was observed for both raw intensity and the genotypes...

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Autores principales: Hong, H, Shi, L, Su, Z, Ge, W, Jones, W D, Czika, W, Miclaus, K, Lambert, C G, Vega, S C, Zhang, J, Ning, B, Liu, J, Green, B, Xu, L, Fang, H, Perkins, R, Lin, S M, Jafari, N, Park, K, Ahn, T, Chierici, M, Furlanello, C, Zhang, L, Wolfinger, R D, Goodsaid, F, Tong, W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928027/
https://www.ncbi.nlm.nih.gov/pubmed/20368714
http://dx.doi.org/10.1038/tpj.2010.24
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author Hong, H
Shi, L
Su, Z
Ge, W
Jones, W D
Czika, W
Miclaus, K
Lambert, C G
Vega, S C
Zhang, J
Ning, B
Liu, J
Green, B
Xu, L
Fang, H
Perkins, R
Lin, S M
Jafari, N
Park, K
Ahn, T
Chierici, M
Furlanello, C
Zhang, L
Wolfinger, R D
Goodsaid, F
Tong, W
author_facet Hong, H
Shi, L
Su, Z
Ge, W
Jones, W D
Czika, W
Miclaus, K
Lambert, C G
Vega, S C
Zhang, J
Ning, B
Liu, J
Green, B
Xu, L
Fang, H
Perkins, R
Lin, S M
Jafari, N
Park, K
Ahn, T
Chierici, M
Furlanello, C
Zhang, L
Wolfinger, R D
Goodsaid, F
Tong, W
author_sort Hong, H
collection PubMed
description The discordance in results of independent genome-wide association studies (GWAS) indicates the potential for Type I and Type II errors. We assessed the repeatibility of current Affymetrix technologies that support GWAS. Reasonable reproducibility was observed for both raw intensity and the genotypes/copy number variants. We also assessed consistencies between different SNP arrays and between genotype calling algorithms. We observed that the inconsistency in genotypes was generally small at the specimen level. To further examine whether the differences from genotyping and genotype calling are possible sources of variation in GWAS results, an association analysis was applied to compare the associated SNPs. We observed that the inconsistency in genotypes not only propagated to the association analysis, but was amplified in the associated SNPs. Our studies show that inconsistencies between SNP arrays and between genotype calling algorithms are potential sources for the lack of reproducibility in GWAS results.
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spelling pubmed-29280272010-08-25 Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples Hong, H Shi, L Su, Z Ge, W Jones, W D Czika, W Miclaus, K Lambert, C G Vega, S C Zhang, J Ning, B Liu, J Green, B Xu, L Fang, H Perkins, R Lin, S M Jafari, N Park, K Ahn, T Chierici, M Furlanello, C Zhang, L Wolfinger, R D Goodsaid, F Tong, W Pharmacogenomics J Original Article The discordance in results of independent genome-wide association studies (GWAS) indicates the potential for Type I and Type II errors. We assessed the repeatibility of current Affymetrix technologies that support GWAS. Reasonable reproducibility was observed for both raw intensity and the genotypes/copy number variants. We also assessed consistencies between different SNP arrays and between genotype calling algorithms. We observed that the inconsistency in genotypes was generally small at the specimen level. To further examine whether the differences from genotyping and genotype calling are possible sources of variation in GWAS results, an association analysis was applied to compare the associated SNPs. We observed that the inconsistency in genotypes not only propagated to the association analysis, but was amplified in the associated SNPs. Our studies show that inconsistencies between SNP arrays and between genotype calling algorithms are potential sources for the lack of reproducibility in GWAS results. Nature Publishing Group 2010-08 2010-04-06 /pmc/articles/PMC2928027/ /pubmed/20368714 http://dx.doi.org/10.1038/tpj.2010.24 Text en Copyright © 2010 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Hong, H
Shi, L
Su, Z
Ge, W
Jones, W D
Czika, W
Miclaus, K
Lambert, C G
Vega, S C
Zhang, J
Ning, B
Liu, J
Green, B
Xu, L
Fang, H
Perkins, R
Lin, S M
Jafari, N
Park, K
Ahn, T
Chierici, M
Furlanello, C
Zhang, L
Wolfinger, R D
Goodsaid, F
Tong, W
Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
title Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
title_full Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
title_fullStr Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
title_full_unstemmed Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
title_short Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
title_sort assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with hapmap samples
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928027/
https://www.ncbi.nlm.nih.gov/pubmed/20368714
http://dx.doi.org/10.1038/tpj.2010.24
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