AMDA

AMDA performs adaptive multivariate two-sample testing to detect differential abundance of microbial taxa between two sample groups in microbiome studies.


Key Features:

  • Multivariate Approach: Evaluates overall shifts in microbial community composition by jointly testing multiple taxa to capture interactions and correlations among taxa.
  • Adaptive Testing Framework: Employs an adaptive testing framework to increase statistical power while controlling type I error rates in high-dimensional microbiome data.
  • Simulation Studies and Real Data Validation: Has been evaluated using simulation studies and applied to real datasets, demonstrating improved power relative to existing methods.
  • Control for Multiple Testing: Accounts for complex dependencies among taxa to mitigate issues arising from multiple comparisons and stringent correction procedures such as false discovery rate control.

Scientific Applications:

  • Disease Association Studies: Identifies shifts in microbiota composition linked to diseases such as inflammatory bowel disease, obesity, and cancer.
  • Environmental Microbiome Research: Analyzes changes in microbial communities in response to environmental factors or interventions.
  • Personalized Medicine: Investigates associations between individual microbiome profiles and treatment responses or health outcomes.

Methodology:

Compares taxa composition between two conditions using an adaptive multivariate statistical test that accounts for high dimensionality and complex correlations among taxa while controlling type I error under multiple testing (e.g., false discovery rate).

Topics

Details

License:
GPL-3.0
Maturity:
Mature
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
8/9/2019
Last Updated:
6/16/2020

Operations

Publications

Banerjee K, Zhao N, Srinivasan A, Xue L, Hicks SD, Middleton FA, Wu R, Zhan X. An Adaptive Multivariate Two-Sample Test With Application to Microbiome Differential Abundance Analysis. Frontiers in Genetics. 2019;10. doi:10.3389/fgene.2019.00350. PMID:31068967. PMCID:PMC6491633.

Documentation

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