4.7 Article

GutBalance: a server for the human gut microbiome-based disease prediction and biomarker discovery with compositionality addressed

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 22, Issue 5, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbaa436

Keywords

microbiome; balance; logistic regression; disease prediction; balance-disease association; microbe-disease association

Funding

  1. National Key Research and Development Program of China [2018YFC0910405]
  2. National Natural Science Foundation of China [61771331, 61922020, 91935302]

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This study highlights the compositional nature of microbiome data and introduces the distal discriminative balance analysis method for building balance-based models for human gut microbiome-related diseases. The concept of balance-disease associations is emphasized, leading to the development of the Human Gut Balance-Disease Association Database (GBDAD). The inference of balance-based species-disease associations can accelerate the generation of new microbe-disease association hypotheses in gastrointestinal microecology research and clinical trials.
The compositionality of the microbiome data is well-known but often neglected. The compositional transformation pertains to the supervised learning of microbiome data and is a critical step that decides the performance and reliability of the disease classifiers. We value the excellent performance of the distal discriminative balance analysis (DBA) method, which selects distal balances of pairs and trios of bacteria, in addressing the classification of high-dimensional microbiome data. By applying this method to the species-level abundances of all the disease phenotypes in the GMrepo database, we build a balance-based model repository for the classification of human gut microbiome-related diseases. The model repository supports the prediction of disease risks for new sample(s). More importantly, we highlight the concept of balance-disease associations rather than the conventional microbe-disease associations and develop the human Gut Balance-Disease Association Database (GBDAD). Each predictable balance for each disease model indicates a potential biomarker-disease relationship and can be interpreted as a bacteria ratio positively or negatively correlated with the disease. Furthermore, by linking the balance-disease associations to the evidenced microbe-disease associations in MicroPhenoDB, we surprisingly found that most species-disease associations inferred from the shotgun metagenomic datasets can be validated by external evidence beyond MicroPhenoDB. The balance-based species-disease association inference will accelerate the generation of new microbe-disease association hypotheses in gastrointestinal microecology research and clinical trials. The model repository and the GBDAD database are deployed on the GutBalance server, which supports interactive visualization and systematic interrogation of the disease models, disease-related balances and disease-related species of interest.

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