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The Joint Null Criterion for Multiple Hypothesis Tests

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  • Leek Jeffrey T
  • Storey John D.

Abstract

Simultaneously performing many hypothesis tests is a problem commonly encountered in high-dimensional biology. In this setting, a large set of p-values is calculated from many related features measured simultaneously. Classical statistics provides a criterion for defining what a “correct” p-value is when performing a single hypothesis test. We show here that even when each p-value is marginally correct under this single hypothesis criterion, it may be the case that the joint behavior of the entire set of p-values is problematic. On the other hand, there are cases where each p-value is marginally incorrect, yet the joint distribution of the set of p-values is satisfactory. Here, we propose a criterion defining a well behaved set of simultaneously calculated p-values that provides precise control of common error rates and we introduce diagnostic procedures for assessing whether the criterion is satisfied with simulations. Multiple testing p-values that satisfy our new criterion avoid potentially large study specific errors, but also satisfy the usual assumptions for strong control of false discovery rates and family-wise error rates. We utilize the new criterion and proposed diagnostics to investigate two common issues in high-dimensional multiple testing for genomics: dependent multiple hypothesis tests and pooled versus test-specific null distributions.

Suggested Citation

  • Leek Jeffrey T & Storey John D., 2011. "The Joint Null Criterion for Multiple Hypothesis Tests," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 10(1), pages 1-22, June.
  • Handle: RePEc:bpj:sagmbi:v:10:y:2011:i:1:n:28
    DOI: 10.2202/1544-6115.1673
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    References listed on IDEAS

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    Cited by:

    1. Segal Mark R. & Xiong Hao & Bengtsson Henrik & Bourgon Richard & Gentleman Robert, 2012. "Querying Genomic Databases: Refining the Connectivity Map," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 11(2), pages 1-37, January.
    2. Wang Chamont & Gevertz Jana L., 2016. "Finding causative genes from high-dimensional data: an appraisal of statistical and machine learning approaches," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 15(4), pages 321-347, August.

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