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Retrospective score tests versus prospective score tests for genetic association with case-control data

  1. Author:
    Liu, Yukun [ORCID]
    Li, Pengfei [ORCID]
    Song,Lei
    Yu, Kai [ORCID]
    Qin, Jing [ORCID]
  2. Author Address

    KLATASDS - MOE, School of Statistics, East China Normal University, Shanghai, 200062, China., Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, ON, Canada, N2L 3G1., National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA., Cancer Genomics Research Laboratory, Leidos Biomedical Research, Inc., Frederick, MD 21704, USA., National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, 20892, USA.,
    1. Year: 2020
    2. Date: Apr 10
    3. Epub Date: 2020 04 10
  1. Journal: Biometrics
  2. Type of Article: Article
  3. ISSN: 0006-341X
  1. Abstract:

    Since the seminal work of Prentice and Pyke (1979), the prospective logistic likelihood has become the standard method of analysis for retrospectively collected case-control data, in particular for testing the association between a single genetic marker and a disease outcome in genetic case-control studies. In the study of multiple genetic markers with relatively small effects, especially those with rare variants, various aggregated approaches based on the same prospective likelihood have been developed to integrate subtle association evidence among all the markers considered. Many of the commonly used tests are derived from the prospective likelihood under a common-random-effect assumption, which assumes a common random effect for all subjects. We develop the locally most powerful aggregation test based on the retrospective likelihood under an independent-random-effect assumption, which allows the genetic effect to vary among subjects. In contrast to the fact that disease prevalence information cannot be used to improve efficiency for the estimation of odds ratio parameters in logistic regression models, we show that it can be utilized to enhance the testing power in genetic association studies. Extensive simulations demonstrate the advantages of the proposed method over the existing ones. A real genome-wide association study is analyzed forĀ illustration. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.

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External Sources

  1. DOI: 10.1111/biom.13270
  2. PMID: 32275064
  3. WOS: 000529820000001

Library Notes

  1. Fiscal Year: FY2019-2020
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