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Test Gene-Environment Interactions for Multiple Traits in Sequencing Association Studies.
Zhang, Jianjun; Sha, Qiuying; Hao, Han; Zhang, Shuanglin; Gao, Xiaoyi Raymond; Wang, Xuexia.
  • Zhang J; Department of Mathematics, University of North Texas, Denton, Texas, USA.
  • Sha Q; Department of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, USA.
  • Hao H; Department of Mathematics, University of North Texas, Denton, Texas, USA.
  • Zhang S; Department of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, USA.
  • Gao XR; Department of Ophthalmology and Visual Science, The Ohio State University, Columbus, Ohio, USA.
  • Wang X; Department of Biomedical Informatics, The Ohio State University, Columbus, Ohio, USA.
Hum Hered ; 84(4-5): 170-196, 2019.
Article en En | MEDLINE | ID: mdl-32417835
ABSTRACT
MOTIVATION The risk of many complex diseases is determined by an interplay of genetic and environmental factors. The examination of gene-environment interactions (G×Es) for multiple traits can yield valuable insights about the etiology of the disease and increase power in detecting disease-associated genes. However, the methods for testing G×Es for multiple traits are very limited.

METHOD:

We developed novel approaches to test G×Es for multiple traits in sequencing association studies. We first perform a transformation of multiple traits by using either principal component analysis or standardization analysis. Then, we detect the effects of G×Es using novel proposed tests testing the effect of an optimally weighted combination of G×Es (TOW-GE) and/or variable weight TOW-GE (VW-TOW-GE). Finally, we employ Fisher's combination test to combine the p values.

RESULTS:

Extensive simulation studies show that the type I error rates of the proposed methods are well controlled. Compared to the interaction sequence kernel association test (ISKAT), TOW-GE is more powerful when there are only rare risk and protective variants; VW-TOW-GE is more powerful when there are both rare and common variants. Both TOW-GE and VW-TOW-GE are robust to directions of effects of causal G×Es. Application to the COPDGene Study demonstrates that our proposed methods are very effective.

CONCLUSIONS:

Our proposed methods are useful tools in the identification of G×Es for multiple traits. The proposed methods can be used not only to identify G×Es for common variants, but also for rare variants. Therefore, they can be employed in identifying G×Es in both genome-wide association studies and next-generation sequencing data analyses.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2019 Tipo del documento: Article