A unified method for detecting secondary trait associations with rare variants: application to sequence data.

TitleA unified method for detecting secondary trait associations with rare variants: application to sequence data.
Publication TypeJournal Article
Year of Publication2012
AuthorsLiu, DJ, Leal, SM
JournalPLoS Genet
Volume8
Issue11
Paginatione1003075
Date Published2012
ISSN1553-7404
KeywordsBlood Pressure, Computer Simulation, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, High-Throughput Nucleotide Sequencing, Humans, Italy, Lipoproteins, LDL, Models, Genetic, Phenotype, Quantitative Trait Loci, Software
Abstract

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.

DOI10.1371/journal.pgen.1003075
Alternate JournalPLoS Genet.
PubMed ID23166519
PubMed Central IDPMC3499373
Grant ListU54 HG006493 / HG / NHGRI NIH HHS / United States
N01-AG-1-2109 / AG / NIA NIH HHS / United States
HG002651 / HG / NHGRI NIH HHS / United States
HG006493 / HG / NHGRI NIH HHS / United States
HL084729 / HL / NHLBI NIH HHS / United States
/ / Intramural NIH HHS / United States
263-MA-410953 / / PHS HHS / United States
HL102926 / HL / NHLBI NIH HHS / United States
UM1 HG006493 / HG / NHGRI NIH HHS / United States
MD005964 / MD / NIMHD NIH HHS / United States
HG005581 / HG / NHGRI NIH HHS / United States