4.3 Article

Sequence Kernel Association Test for Survival Traits

期刊

GENETIC EPIDEMIOLOGY
卷 38, 期 3, 页码 191-197

出版社

WILEY
DOI: 10.1002/gepi.21791

关键词

rare variant analysis; variance component test; likelihood ratio test; Cox proportional hazard model

资金

  1. NIH [R01DK078616, U01 DK85526, K24 DK080140]
  2. National Heart, Lung, and Blood Institute (NHLBI)
  3. Boston University [N01-HC-25195]
  4. Affymetrix, Inc for genotyping services [N02-HL-6-4278]

向作者/读者索取更多资源

Rare variant tests have been of great interest in testing genetic associations with diseases and disease-related quantitative traits in recent years. Among these tests, the sequence kernel association test (SKAT) is an omnibus test for effects of rare genetic variants, in a linear or logistic regression framework. It is often described as a variance component test treating the genotypic effects as random. When the linear kernel is used, its test statistic can be expressed as a weighted sum of single-marker score test statistics. In this paper, we extend the test to survival phenotypes in a Cox regression framework. Because of the anticonservative small-sample performance of the score test in a Cox model, we substitute signed square-root likelihood ratio statistics for the score statistics, and confirm that the small-sample control of type I error is greatly improved. This test can also be applied in meta-analysis. We show in our simulation studies that this test has superior statistical power except in a few specific scenarios, as compared to burden tests in a Cox model. We also present results in an application to time-to-obesity using genotypes from Framingham Heart Study SNP Health Association Resource.

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