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A Genomic Background Based Method for Association Analysis in Related Individuals

BACKGROUND: Feasibility of genotyping of hundreds and thousands of single nucleotide polymorphisms (SNPs) in thousands of study subjects have triggered the need for fast, powerful, and reliable methods for genome-wide association analysis. Here we consider a situation when study participants are gen...

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Autores principales: Amin, Najaf, van Duijn, Cornelia M., Aulchenko, Yurii S.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2093991/
https://www.ncbi.nlm.nih.gov/pubmed/18060068
http://dx.doi.org/10.1371/journal.pone.0001274
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author Amin, Najaf
van Duijn, Cornelia M.
Aulchenko, Yurii S.
author_facet Amin, Najaf
van Duijn, Cornelia M.
Aulchenko, Yurii S.
author_sort Amin, Najaf
collection PubMed
description BACKGROUND: Feasibility of genotyping of hundreds and thousands of single nucleotide polymorphisms (SNPs) in thousands of study subjects have triggered the need for fast, powerful, and reliable methods for genome-wide association analysis. Here we consider a situation when study participants are genetically related (e.g. due to systematic sampling of families or because a study was performed in a genetically isolated population). Of the available methods that account for relatedness, the Measured Genotype (MG) approach is considered the ‘gold standard’. However, MG is not efficient with respect to time taken for the analysis of genome-wide data. In this context we proposed a fast two-step method called Genome-wide Association using Mixed Model and Regression (GRAMMAR) for the analysis of pedigree-based quantitative traits. This method certainly overcomes the drawback of time limitation of the measured genotype (MG) approach, but pays in power. One of the major drawbacks of both MG and GRAMMAR, is that they crucially depend on the availability of complete and correct pedigree data, which is rarely available. METHODOLOGY: In this study we first explore type 1 error and relative power of MG, GRAMMAR, and Genomic Control (GC) approaches for genetic association analysis. Secondly, we propose an extension to GRAMMAR i.e. GRAMMAR-GC. Finally, we propose application of GRAMMAR-GC using the kinship matrix estimated through genomic marker data, instead of (possibly missing and/or incorrect) genealogy. CONCLUSION: Through simulations we show that MG approach maintains high power across a range of heritabilities and possible pedigree structures, and always outperforms other contemporary methods. We also show that the power of our proposed GRAMMAR-GC approaches to that of the ‘gold standard’ MG for all models and pedigrees studied. We show that this method is both feasible and powerful and has correct type 1 error in the context of genome-wide association analysis in related individuals.
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spelling pubmed-20939912007-12-05 A Genomic Background Based Method for Association Analysis in Related Individuals Amin, Najaf van Duijn, Cornelia M. Aulchenko, Yurii S. PLoS One Research Article BACKGROUND: Feasibility of genotyping of hundreds and thousands of single nucleotide polymorphisms (SNPs) in thousands of study subjects have triggered the need for fast, powerful, and reliable methods for genome-wide association analysis. Here we consider a situation when study participants are genetically related (e.g. due to systematic sampling of families or because a study was performed in a genetically isolated population). Of the available methods that account for relatedness, the Measured Genotype (MG) approach is considered the ‘gold standard’. However, MG is not efficient with respect to time taken for the analysis of genome-wide data. In this context we proposed a fast two-step method called Genome-wide Association using Mixed Model and Regression (GRAMMAR) for the analysis of pedigree-based quantitative traits. This method certainly overcomes the drawback of time limitation of the measured genotype (MG) approach, but pays in power. One of the major drawbacks of both MG and GRAMMAR, is that they crucially depend on the availability of complete and correct pedigree data, which is rarely available. METHODOLOGY: In this study we first explore type 1 error and relative power of MG, GRAMMAR, and Genomic Control (GC) approaches for genetic association analysis. Secondly, we propose an extension to GRAMMAR i.e. GRAMMAR-GC. Finally, we propose application of GRAMMAR-GC using the kinship matrix estimated through genomic marker data, instead of (possibly missing and/or incorrect) genealogy. CONCLUSION: Through simulations we show that MG approach maintains high power across a range of heritabilities and possible pedigree structures, and always outperforms other contemporary methods. We also show that the power of our proposed GRAMMAR-GC approaches to that of the ‘gold standard’ MG for all models and pedigrees studied. We show that this method is both feasible and powerful and has correct type 1 error in the context of genome-wide association analysis in related individuals. Public Library of Science 2007-12-05 /pmc/articles/PMC2093991/ /pubmed/18060068 http://dx.doi.org/10.1371/journal.pone.0001274 Text en Amin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Amin, Najaf
van Duijn, Cornelia M.
Aulchenko, Yurii S.
A Genomic Background Based Method for Association Analysis in Related Individuals
title A Genomic Background Based Method for Association Analysis in Related Individuals
title_full A Genomic Background Based Method for Association Analysis in Related Individuals
title_fullStr A Genomic Background Based Method for Association Analysis in Related Individuals
title_full_unstemmed A Genomic Background Based Method for Association Analysis in Related Individuals
title_short A Genomic Background Based Method for Association Analysis in Related Individuals
title_sort genomic background based method for association analysis in related individuals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2093991/
https://www.ncbi.nlm.nih.gov/pubmed/18060068
http://dx.doi.org/10.1371/journal.pone.0001274
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