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Detecting sparse microbial association signals adaptively from longitudinal microbiome data based on generalized estimating equations.
Sun, Han; Huang, Xiaoyun; Huo, Ban; Tan, Yuting; He, Tingting; Jiang, Xingpeng.
Affiliation
  • Sun H; School of Mathematics and Statistics, Central China Normal University, Wuhan 430079, China.
  • Huang X; Hubei Provincial Key Laboratory of Artificial Intelligence and Smart Learning, Central China Normal University, Wuhan 430079, China.
  • Huo B; Hubei Provincial Key Laboratory of Artificial Intelligence and Smart Learning, Central China Normal University, Wuhan 430079, China.
  • Tan Y; Collaborative & Innovative Center for Educational Technology, Central China Normal University, Wuhan 430079, China.
  • He T; Hubei Provincial Key Laboratory of Artificial Intelligence and Smart Learning, Central China Normal University, Wuhan 430079, China.
  • Jiang X; School of Computer, Central China Normal University, Wuhan 430079, China.
Brief Bioinform ; 23(5)2022 09 20.
Article in En | MEDLINE | ID: mdl-35561307
ABSTRACT
The association between the compositions of microbial communities and various host phenotypes is an important research topic. Microbiome association research addresses multiple domains, such as human disease and diet. Statistical methods for testing microbiome-phenotype associations have been studied recently to determine their ability to assess longitudinal microbiome data. However, existing methods fail to detect sparse association signals in longitudinal microbiome data. In this paper, we developed a novel method, namely aGEEMIHC, which is a data-driven adaptive microbiome higher criticism analysis based on generalized estimating equations to detect sparse microbial association signals from longitudinal microbiome data. aGEEMiHC adopts generalized estimating equations framework that fully considers the correlation among different observations from the same subject in longitudinal data. To be robust to diverse correlation structures for longitudinal data, aGEEMiHC integrates multiple microbiome higher criticism analyses based on generalized estimating equations with different working correlation structures. Extensive simulation experiments demonstrate that aGEEMiHC can control the type I error correctly and achieve superior performance according to a statistical power comparison. We also applied it to longitudinal microbiome data with various types of host phenotypes to demonstrate the stability of our method. aGEEMiHC is also utilized for real longitudinal microbiome data, and we found a significant association between the gut microbiome and Crohn's disease. In addition, our method ranks the significant factors associated with the host phenotype to provide potential biomarkers.
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Full text: 1 Database: MEDLINE Main subject: Crohn Disease / Microbiota / Gastrointestinal Microbiome Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Crohn Disease / Microbiota / Gastrointestinal Microbiome Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Year: 2022 Type: Article