| Literature DB >> 34555324 |
Yara Seif1, Bernhard Ørn Palsson2.
Abstract
Genome-scale models of metabolism (GEMs) are key computational tools for the systems-level study of metabolic networks. Here, we describe the "GEM life cycle," which we subdivide into four stages: inception, maturation, specialization, and amalgamation. We show how different types of GEM reconstruction workflows fit in each stage and proceed to highlight two fundamental bottlenecks for GEM quality improvement: GEM maturation and content removal. We identify common characteristics contributing to increasing quality of maturing GEMs drawing from past independent GEM maturation efforts. We then shed some much-needed light on the latent and unrecognized but pervasive issue of content removal, demonstrating the substantial effects of model pruning on its solution space. Finally, we propose a novel framework for content removal and associated confidence-level assignment which will help guide future GEM development efforts, reduce duplication of effort across groups, potentially aid automated reconstruction platforms, and boost the reproducibility of model development.Entities:
Keywords: functional annotation; metabolic modeling; metabolic reconstructions; systems biology
Mesh:
Year: 2021 PMID: 34555324 PMCID: PMC8480436 DOI: 10.1016/j.cels.2021.06.005
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 11.091