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A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data
Next-generation sequencing has made possible the detection of rare variant (RV) associations with quantitative traits (QT). Due to high sequencing cost, many studies can only sequence a modest number of selected samples with extreme QT. Therefore association testing in individual studies can be unde...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499373/ https://www.ncbi.nlm.nih.gov/pubmed/23166519 http://dx.doi.org/10.1371/journal.pgen.1003075 |
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author | Liu, Dajiang J. Leal, Suzanne M. |
author_facet | Liu, Dajiang J. Leal, Suzanne M. |
author_sort | Liu, Dajiang J. |
collection | PubMed |
description | Next-generation sequencing has made possible the detection of rare variant (RV) associations with quantitative traits (QT). Due to high sequencing cost, many studies can only sequence a modest number of selected samples with extreme QT. Therefore association testing in individual studies can be underpowered. Besides the primary trait, many clinically important secondary traits are often measured. It is highly beneficial if multiple studies can be jointly analyzed for detecting associations with commonly measured traits. However, analyzing secondary traits in selected samples can be biased if sample ascertainment is not properly modeled. Some methods exist for analyzing secondary traits in selected samples, where some burden tests can be implemented. However p-values can only be evaluated analytically via asymptotic approximations, which may not be accurate. Additionally, potentially more powerful sequence kernel association tests, variable selection-based methods, and burden tests that require permutations cannot be incorporated. To overcome these limitations, we developed a unified method for analyzing secondary trait associations with RVs (STAR) in selected samples, incorporating all RV tests. Statistical significance can be evaluated either through permutations or analytically. STAR makes it possible to apply more powerful RV tests to analyze secondary trait associations. It also enables jointly analyzing multiple cohorts ascertained under different study designs, which greatly boosts power. The performance of STAR and commonly used RV association tests were comprehensively evaluated using simulation studies. STAR was also implemented to analyze a dataset from the SardiNIA project where samples with extreme low-density lipoprotein levels were sequenced. A significant association between LDLR and systolic blood pressure was identified, which is supported by pharmacogenetic studies. In summary, for sequencing studies, STAR is an important tool for detecting secondary-trait RV associations. |
format | Online Article Text |
id | pubmed-3499373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34993732012-11-19 A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data Liu, Dajiang J. Leal, Suzanne M. PLoS Genet Research Article Next-generation sequencing has made possible the detection of rare variant (RV) associations with quantitative traits (QT). Due to high sequencing cost, many studies can only sequence a modest number of selected samples with extreme QT. Therefore association testing in individual studies can be underpowered. Besides the primary trait, many clinically important secondary traits are often measured. It is highly beneficial if multiple studies can be jointly analyzed for detecting associations with commonly measured traits. However, analyzing secondary traits in selected samples can be biased if sample ascertainment is not properly modeled. Some methods exist for analyzing secondary traits in selected samples, where some burden tests can be implemented. However p-values can only be evaluated analytically via asymptotic approximations, which may not be accurate. Additionally, potentially more powerful sequence kernel association tests, variable selection-based methods, and burden tests that require permutations cannot be incorporated. To overcome these limitations, we developed a unified method for analyzing secondary trait associations with RVs (STAR) in selected samples, incorporating all RV tests. Statistical significance can be evaluated either through permutations or analytically. STAR makes it possible to apply more powerful RV tests to analyze secondary trait associations. It also enables jointly analyzing multiple cohorts ascertained under different study designs, which greatly boosts power. The performance of STAR and commonly used RV association tests were comprehensively evaluated using simulation studies. STAR was also implemented to analyze a dataset from the SardiNIA project where samples with extreme low-density lipoprotein levels were sequenced. A significant association between LDLR and systolic blood pressure was identified, which is supported by pharmacogenetic studies. In summary, for sequencing studies, STAR is an important tool for detecting secondary-trait RV associations. Public Library of Science 2012-11-15 /pmc/articles/PMC3499373/ /pubmed/23166519 http://dx.doi.org/10.1371/journal.pgen.1003075 Text en © 2012 Liu, Leal 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 Liu, Dajiang J. Leal, Suzanne M. A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data |
title | A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data |
title_full | A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data |
title_fullStr | A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data |
title_full_unstemmed | A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data |
title_short | A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data |
title_sort | unified method for detecting secondary trait associations with rare variants: application to sequence data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499373/ https://www.ncbi.nlm.nih.gov/pubmed/23166519 http://dx.doi.org/10.1371/journal.pgen.1003075 |
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