4.6 Article

A Powerful Gene-Based Test Accommodating Common and Low-Frequency Variants to Detect Both Main Effects and Gene-Gene Interaction Effects in Case-Control Studies

期刊

FRONTIERS IN GENETICS
卷 8, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2017.00228

关键词

gene-gene interaction; next-generation sequencing; case-control study; rare variant association; simulations; autism spectrum disorders; association test

资金

  1. ARRA
  2. Medical Research Council [G0601030]
  3. Wellcome Trust [075491/Z/04]
  4. National Health Research Institutes [PH-106-PP-10]
  5. Ministry of Science and Technology [MOST 104-2221-E-400-004-MY2]
  6. [R01-MH089208]
  7. [R01-MH089175]
  8. [R01-MH089025]
  9. [R01-MH089004]
  10. [R01-MH089482]

向作者/读者索取更多资源

Next-generation sequencing (NGS) has been widely used in genetic association studies to identify both common and rare variants associated with complex diseases. Various statistical association tests have been developed to analyze NGS data; however, most focus on identifying the marginal effects of a set of genetic variants on the disease. Only a few association tests for NGS data analysis have considered the interaction effects between genes. We developed three powerful gene-based gene-gene interaction tests for testing both the main effects and the interaction effects of common, low-frequency, and common with low-frequency variant pairs between two genes (the IGOF tests) in case-control studies using NGS data. We performed a comprehensive simulation study to verify that the proposed tests had appropriate type I error rates and significantly higher power than did other interaction tests for analyzing NGS data. The tests were applied to a whole-exome sequencing dataset for autism spectrum disorder (ASD) and the significant results were evaluated in another independent ASD cohort. The IGOF tests were implemented in C++ and are available at http://igof.sourceforge.net.

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