This article provides a systematic comparative analysis of three prominent automated genome-scale metabolic model (GEM) reconstruction tools: CarveMe, gapseq, and KBase.
This article provides a systematic benchmarking analysis of three topology-based gap-filling algorithms for genome-scale metabolic models (GEMs): CHESHIRE, NHP, and C3MM.
This article provides a comprehensive examination of ATP futile cycles in genome-scale metabolic models (GEMs), addressing both their biological significance as energy-dissipating mechanisms and their role as potential sources of...
Accurate prediction of phenotype and cellular interactions using compartmentalized, constraint-based metabolic models is critically dependent on the completeness and accuracy of transporter annotations.
Gap-filling is a critical but computationally intensive step in refining genome-scale metabolic models (GEMs), directly impacting their predictive accuracy in drug discovery and systems biology.
Community metabolic models, which simulate the interactions of multiple microorganisms, are powerful tools for understanding complex biological systems relevant to human health and disease.
Dead-end metabolites (DEMs)—compounds produced or consumed without a complete pathway—represent significant gaps in our understanding of metabolic networks and hinder the predictive accuracy of genome-scale models.
Stoichiometric inconsistencies in genome-scale metabolic models (GSMMs) present significant challenges in biomedical research, leading to inaccurate flux predictions and limiting their utility in drug discovery and metabolic engineering.
This article provides a comprehensive overview of the DEMETER (Data-drivEn METabolic nEtwork Refinement) pipeline, a computational tool for the efficient, simultaneous curation of genome-scale metabolic reconstructions.
This article provides a comprehensive overview of the COMMIT (Consideration of Metabolite Leakage and Community Composition) approach for gap-filling genome-scale metabolic models of microbial communities.