Inference of differential gene regulatory networks using boosted differential trees

Author:

Galindez Gihanna12ORCID,List Markus3ORCID,Baumbach Jan45ORCID,Völker Uwe6ORCID,Mäder Ulrike6,Blumenthal David B7ORCID,Kacprowski Tim12ORCID

Affiliation:

1. Division Data Science in Biomedicine, Peter L. Reichertz Institute for Medical Informatics of Technische Universität Braunschweig and Hannover Medical School , Braunschweig, 38106, Germany

2. Braunschweig Integrated Centre of Systems Biology (BRICS), TU Braunschweig , Braunschweig, 38106, Germany

3. Experimental Bioinformatics, TUM School of Life Sciences, Technical University of Munich , Munich, 85354, Germany

4. Institute for Computational Systems Biology, University of Hamburg , Hamburg, 22607, Germany

5. Computational Biomedicine Lab, Department of Mathematics and Computer Science, University of Southern Denmark , Odense, 5230, Denmark

6. Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald , Greifswald, 17475, Germany

7. Biomedical Network Science Lab, Department of Artificial Intelligence in Biomedical Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg , Erlangen, 91052, Germany

Abstract

Abstract Summary Diseases can be caused by molecular perturbations that induce specific changes in regulatory interactions and their coordinated expression, also referred to as network rewiring. However, the detection of complex changes in regulatory connections remains a challenging task and would benefit from the development of novel nonparametric approaches. We develop a new ensemble method called BoostDiff (boosted differential regression trees) to infer a differential network discriminating between two conditions. BoostDiff builds an adaptively boosted (AdaBoost) ensemble of differential trees with respect to a target condition. To build the differential trees, we propose differential variance improvement as a novel splitting criterion. Variable importance measures derived from the resulting models are used to reflect changes in gene expression predictability and to build the output differential networks. BoostDiff outperforms existing differential network methods on simulated data evaluated in four different complexity settings. We then demonstrate the power of our approach when applied to real transcriptomics data in COVID-19, Crohn’s disease, breast cancer, prostate adenocarcinoma, and stress response in Bacillus subtilis. BoostDiff identifies context-specific networks that are enriched with genes of known disease-relevant pathways and complements standard differential expression analyses. Availability and implementation BoostDiff is available at https://github.com/scibiome/boostdiff_inference.

Funder

German Federal Ministry of Education and Research

Publisher

Oxford University Press (OUP)

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