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A powerful test for multiple rare variants association studies that incorporates sequencing qualities

Next-generation sequencing data will soon become routinely available for association studies between complex traits and rare variants. Sequencing data, however, are characterized by the presence of sequencing errors at each individual genotype. This makes it especially challenging to perform associa...

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Detalles Bibliográficos
Autores principales: Daye, Z. John, Li, Hongzhe, Wei, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340416/
https://www.ncbi.nlm.nih.gov/pubmed/22262732
http://dx.doi.org/10.1093/nar/gks024
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author Daye, Z. John
Li, Hongzhe
Wei, Zhi
author_facet Daye, Z. John
Li, Hongzhe
Wei, Zhi
author_sort Daye, Z. John
collection PubMed
description Next-generation sequencing data will soon become routinely available for association studies between complex traits and rare variants. Sequencing data, however, are characterized by the presence of sequencing errors at each individual genotype. This makes it especially challenging to perform association studies of rare variants, which, due to their low minor allele frequencies, can be easily perturbed by genotype errors. In this article, we develop the quality-weighted multivariate score association test (qMSAT), a new procedure that allows powerful association tests between complex traits and multiple rare variants under the presence of sequencing errors. Simulation results based on quality scores from real data show that the qMSAT often dominates over current methods, that do not utilize quality information. In particular, the qMSAT can dramatically increase power over existing methods under moderate sample sizes and relatively low coverage. Moreover, in an obesity data study, we identified using the qMSAT two functional regions (MGLL promoter and MGLL 3′-untranslated region) where rare variants are associated with extreme obesity. Due to the high cost of sequencing data, the qMSAT is especially valuable for large-scale studies involving rare variants, as it can potentially increase power without additional experimental cost. qMSAT is freely available at http://qmsat.sourceforge.net/.
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spelling pubmed-33404162012-05-01 A powerful test for multiple rare variants association studies that incorporates sequencing qualities Daye, Z. John Li, Hongzhe Wei, Zhi Nucleic Acids Res Methods Online Next-generation sequencing data will soon become routinely available for association studies between complex traits and rare variants. Sequencing data, however, are characterized by the presence of sequencing errors at each individual genotype. This makes it especially challenging to perform association studies of rare variants, which, due to their low minor allele frequencies, can be easily perturbed by genotype errors. In this article, we develop the quality-weighted multivariate score association test (qMSAT), a new procedure that allows powerful association tests between complex traits and multiple rare variants under the presence of sequencing errors. Simulation results based on quality scores from real data show that the qMSAT often dominates over current methods, that do not utilize quality information. In particular, the qMSAT can dramatically increase power over existing methods under moderate sample sizes and relatively low coverage. Moreover, in an obesity data study, we identified using the qMSAT two functional regions (MGLL promoter and MGLL 3′-untranslated region) where rare variants are associated with extreme obesity. Due to the high cost of sequencing data, the qMSAT is especially valuable for large-scale studies involving rare variants, as it can potentially increase power without additional experimental cost. qMSAT is freely available at http://qmsat.sourceforge.net/. Oxford University Press 2012-04 2012-01-19 /pmc/articles/PMC3340416/ /pubmed/22262732 http://dx.doi.org/10.1093/nar/gks024 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Daye, Z. John
Li, Hongzhe
Wei, Zhi
A powerful test for multiple rare variants association studies that incorporates sequencing qualities
title A powerful test for multiple rare variants association studies that incorporates sequencing qualities
title_full A powerful test for multiple rare variants association studies that incorporates sequencing qualities
title_fullStr A powerful test for multiple rare variants association studies that incorporates sequencing qualities
title_full_unstemmed A powerful test for multiple rare variants association studies that incorporates sequencing qualities
title_short A powerful test for multiple rare variants association studies that incorporates sequencing qualities
title_sort powerful test for multiple rare variants association studies that incorporates sequencing qualities
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340416/
https://www.ncbi.nlm.nih.gov/pubmed/22262732
http://dx.doi.org/10.1093/nar/gks024
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