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Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins

Despite a strong genetic background in cognitive function only a limited number of single nucleotide polymorphisms (SNPs) have been found in genome-wide association studies (GWASs). We hypothesize that this is partially due to mis-specified modeling concerning phenotype distribution as well as the r...

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Autores principales: Mohammadnejad, Afsaneh, Nygaard, Marianne, Li, Shuxia, Zhang, Dongfeng, Xu, Chunsheng, Li, Weilong, Lund, Jesper, Christiansen, Lene, Baumbach, Jan, Christensen, Kaare, Hjelmborg, Jacob v. B., Tan, Qihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746382/
https://www.ncbi.nlm.nih.gov/pubmed/33232274
http://dx.doi.org/10.18632/aging.104198
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author Mohammadnejad, Afsaneh
Nygaard, Marianne
Li, Shuxia
Zhang, Dongfeng
Xu, Chunsheng
Li, Weilong
Lund, Jesper
Christiansen, Lene
Baumbach, Jan
Christensen, Kaare
Hjelmborg, Jacob v. B.
Tan, Qihua
author_facet Mohammadnejad, Afsaneh
Nygaard, Marianne
Li, Shuxia
Zhang, Dongfeng
Xu, Chunsheng
Li, Weilong
Lund, Jesper
Christiansen, Lene
Baumbach, Jan
Christensen, Kaare
Hjelmborg, Jacob v. B.
Tan, Qihua
author_sort Mohammadnejad, Afsaneh
collection PubMed
description Despite a strong genetic background in cognitive function only a limited number of single nucleotide polymorphisms (SNPs) have been found in genome-wide association studies (GWASs). We hypothesize that this is partially due to mis-specified modeling concerning phenotype distribution as well as the relationship between SNP dosage and the level of the phenotype. To overcome these issues, we introduced an assumption-free method based on generalized correlation coefficient (GCC) in a GWAS of cognitive function in Danish and Chinese twins to compare its performance with traditional linear models. The GCC-based GWAS identified two significant SNPs in Danish samples (rs71419535, p = 1.47e-08; rs905838, p = 1.69e-08) and two significant SNPs in Chinese samples (rs2292999, p = 9.27e-10; rs17019635, p = 2.50e-09). In contrast, linear models failed to detect any genome-wide significant SNPs. The number of top significant genes overlapping between the two samples in the GCC-based GWAS was higher than when applying linear models. The GCC model identified significant genetic variants missed by conventional linear models, with more replicated genes and biological pathways related to cognitive function. Moreover, the GCC-based GWAS was robust in handling correlated samples like twin pairs. GCC is a useful statistical method for GWAS that complements traditional linear models for capturing genetic effects beyond the additive assumption.
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spelling pubmed-77463822021-01-04 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins Mohammadnejad, Afsaneh Nygaard, Marianne Li, Shuxia Zhang, Dongfeng Xu, Chunsheng Li, Weilong Lund, Jesper Christiansen, Lene Baumbach, Jan Christensen, Kaare Hjelmborg, Jacob v. B. Tan, Qihua Aging (Albany NY) Research Paper Despite a strong genetic background in cognitive function only a limited number of single nucleotide polymorphisms (SNPs) have been found in genome-wide association studies (GWASs). We hypothesize that this is partially due to mis-specified modeling concerning phenotype distribution as well as the relationship between SNP dosage and the level of the phenotype. To overcome these issues, we introduced an assumption-free method based on generalized correlation coefficient (GCC) in a GWAS of cognitive function in Danish and Chinese twins to compare its performance with traditional linear models. The GCC-based GWAS identified two significant SNPs in Danish samples (rs71419535, p = 1.47e-08; rs905838, p = 1.69e-08) and two significant SNPs in Chinese samples (rs2292999, p = 9.27e-10; rs17019635, p = 2.50e-09). In contrast, linear models failed to detect any genome-wide significant SNPs. The number of top significant genes overlapping between the two samples in the GCC-based GWAS was higher than when applying linear models. The GCC model identified significant genetic variants missed by conventional linear models, with more replicated genes and biological pathways related to cognitive function. Moreover, the GCC-based GWAS was robust in handling correlated samples like twin pairs. GCC is a useful statistical method for GWAS that complements traditional linear models for capturing genetic effects beyond the additive assumption. Impact Journals 2020-11-24 /pmc/articles/PMC7746382/ /pubmed/33232274 http://dx.doi.org/10.18632/aging.104198 Text en Copyright: © 2020 Mohammadnejad et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Mohammadnejad, Afsaneh
Nygaard, Marianne
Li, Shuxia
Zhang, Dongfeng
Xu, Chunsheng
Li, Weilong
Lund, Jesper
Christiansen, Lene
Baumbach, Jan
Christensen, Kaare
Hjelmborg, Jacob v. B.
Tan, Qihua
Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
title Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
title_full Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
title_fullStr Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
title_full_unstemmed Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
title_short Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
title_sort generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746382/
https://www.ncbi.nlm.nih.gov/pubmed/33232274
http://dx.doi.org/10.18632/aging.104198
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