eudysbiome

eudysbiome annotates and classifies differential genera in mammalian microbiomes, particularly in the gut-intestinal (GI) ecosystem, to assess their potential contribution to host diseases and categorize them as harmful, harmless, or unknown.


Key Features:

  • Annotation of Genera: Automatically annotates pathogenic and non-pathogenic genera within the microbiome to distinguish harmful, harmless, or unknown taxa.
  • Quantitative Assessment: Quantitatively evaluates the net variation in frequency of harmless versus harmful organisms to determine eubiotic or dysbiotic impacts.
  • Global Composition Analysis: Evaluates the global composition of the microbiome rather than focusing solely on metrics such as α-diversity or the Firmicutes to Bacteroides ratio.
  • Integration with Existing Approaches: Complements and integrates with existing metagenomic analyses to provide systemic-level interpretation of microbial composition changes.
  • Application in Clinical Research: Applied to human GI-microbiome data to characterize physiological effects of treatments such as Prednisone and Methotrexate for rheumatoid arthritis (RA).
  • Computational Efficiency: Implements computationally efficient procedures to address challenges from incomplete species functional knowledge when analyzing large datasets.

Scientific Applications:

  • Disease Progression Studies: Quantifies shifts in harmful versus harmless taxa to study microbiome-associated disease progression.
  • Therapy Impact Assessment: Assesses long-term effects of therapies on the GI microbiome, including responses to Prednisone and Methotrexate in RA.
  • Clinical Interpretation: Provides quantitative evidence to inform clinical decision-making and therapeutic development based on microbial composition changes.

Methodology:

Automatic annotation of genera, quantitative evaluation of net frequency variation between harmless and harmful organisms, global composition analysis, and integration with metagenomic analyses.

Topics

Collections

Details

Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
11/8/2015
Last Updated:
11/25/2024

Operations

Publications

Zhou X, Nardini C. A method for automated pathogenic content estimation with application to rheumatoid arthritis. BMC Systems Biology. 2016;10(1). doi:10.1186/s12918-016-0344-6. PMID:27846901. PMCID:PMC5111251.

PMID: 27846901
PMCID: PMC5111251
Funding: - National Natural Science Foundation of China: 31171277

Documentation

Links

Software catalogue
http://bioconductor.org/