Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 6 min ago
PreprintarXiv licencearXiv

Global Testing of Gaussian Means by Combining Marginal and Conditional Evidence

Abstract

We propose a test of the global null hypothesis of zero means in correlated multivariate Gaussian data by combining marginal and conditional evidence at each coordinate. The conditional tests are based on the distribution of each coordinate given the remaining coordinates. At each coordinate, the corresponding two-sided p-values are combined using the Simes method, followed by a Bonferroni correction across coordinates. Because conditioning can either strengthen or weaken evidence against the null, neither marginal nor conditional testing is uniformly preferable. The proposed procedure adapts to their relative strengths while retaining the simplicity of minimum-type global testing. We establish finite-sample control of the global Type-I error under both known covariance and covariance estimated from an independent sample. The latter setting requires a careful analysis of the dependence between studentized marginal and conditional statistics. We evaluate the power of the proposed test through simulations, compare its performance with existing global tests, and illustrate its practical utility using a TCGA carcinoma dataset.

Related

  1. Conditional independence testing through marginal permutation
    Jiahao Ai, Ziang Niu
    arXivPreprintCC BY 4.0Full textStatisticsarXiv
  2. Does your cost-effectiveness model answer the question of interest? Marginal versus conditional inputs and transportability across populations
    Jeroen P. Jansen, Harlan Campbell, Shannon Cope +2
    arXivPreprintCC BY 4.0Full textStatisticsarXiv
  3. Conditional and Marginal Run-Length Quantiles of Gamma CUSUM Charts with an Estimated Scale: Tail Integrability and One-Point MRL Protection
    Yulong Qiao, Qian Zhang, Bin Dai +2
    AxiomsPeer-reviewedCC BY 4.0General mathematicsCrossref
  4. Beyond Marginal Monitoring: Distributed Joint-Distribution Testing for Data Concept Drift in Large Scale E-Commerce Operations
    Cagdas Pullu, Mahmut Emir Arslan, Bugra Balkac +4
    arXivPreprintarXiv licenceFull textStatisticsarXiv
  5. Asymptotic Theory for Combining Dependent p-Values for Global Hypothesis Testing
    Haoyi Yang, Lingzhou Xue
    arXivPreprintarXiv licenceFull textStatisticsarXiv
BibTeX
@misc{ghosh2026global,
  title = {{Global Testing of Gaussian Means by Combining Marginal and Conditional Evidence}},
  author = {Deepra Ghosh and Edgar Dobriban and Sanat K. Sarkar},
  howpublished = {arXiv},
  year = {2026},
  month = oct,
  doi = {10.48550/arxiv.2610.40899},
  eprint = {2610.40899},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2610.40899},
}
RIS
TY  - UNPB
TI  - Global Testing of Gaussian Means by Combining Marginal and Conditional Evidence
AU  - Deepra Ghosh
AU  - Edgar Dobriban
AU  - Sanat K. Sarkar
PY  - 2026
DA  - 2026/10/29
PB  - arXiv
DO  - 10.48550/arxiv.2610.40899
UR  - https://arxiv.org/abs/2610.40899
AB  - We propose a test of the global null hypothesis of zero means in correlated multivariate Gaussian data by combining marginal and conditional evidence at each coordinate. The conditional tests are based on the distribution of each coordinate given the remaining coordinates. At each coordinate, the corresponding two-sided p-values are combined using the Simes method, followed by a Bonferroni correction across coordinates. Because conditioning can either strengthen or weaken evidence against the null, neither marginal nor conditional testing is uniformly preferable. The proposed procedure adapts to their relative strengths while retaining the simplicity of minimum-type global testing. We establish finite-sample control of the global Type-I error under both known covariance and covariance estimated from an independent sample. The latter setting requires a careful analysis of the dependence between studentized marginal and conditional statistics. We evaluate the power of the proposed test through simulations, compare its performance with existing global tests, and illustrate its practical utility using a TCGA carcinoma dataset.
ER  -