Abstract

Next-generation sequencing has paved the way for the reconstruction of genome-scale metabolic networks as a powerful tool for understanding metabolic circuits in any organism. However, the visualization and extraction of knowledge from these large networks comprising thousands of reactions and metabolites is a current challenge in need of user-friendly tools. Here we present Fluxer (https://fluxer.umbc.edu), a free and open-access novel web application for the computation and visualization of genome-scale metabolic flux networks. Any genome-scale model based on the Systems Biology Markup Language can be uploaded to the tool, which automatically performs Flux Balance Analysis and computes different flux graphs for visualization and analysis. The major metabolic pathways for biomass growth or for biosynthesis of any metabolite can be interactively knocked-out, analyzed and visualized as a spanning tree, dendrogram or complete graph using different layouts. In addition, Fluxer can compute and visualize the k-shortest metabolic paths between any two metabolites or reactions to identify the main metabolic routes between two compounds of interest. The web application includes >80 whole-genome metabolic reconstructions of diverse organisms from bacteria to human, readily available for exploration. Fluxer enables the efficient analysis and visualization of genome-scale metabolic models toward the discovery of key metabolic pathways.

Highlights

  • Metabolic reconstructions from whole-genome sequencing and biochemical data aim to determine all metabolic processes occurring within a cell or whole organism, which can be integrated into genome-scale metabolic models (GEMs) able to predict cellular phenotypes [1,2]

  • We presented here Fluxer, a user-friendly web application for the computation, analysis and visualization of flux graphs for GEMs

  • The tool can perform Flux Balance Analysis (FBA) including specific reaction knockouts and compute metabolic network representations based on spanning trees, k-shortest paths and complete graphs

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Summary

Introduction

Metabolic reconstructions from whole-genome sequencing and biochemical data aim to determine all metabolic processes occurring within a cell or whole organism, which can be integrated into genome-scale metabolic models (GEMs) able to predict cellular phenotypes [1,2]. There is a need for user-friendly tools based on robust graph-theory methods [21,22,23,24] that can automatically visualize with efficient and clean layouts a complete GEM and its FBA solution fluxes directly from an SBML model.

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