Path to improving the life cycle and quality of genome-scale models of metabolism

Yara Seif, Bernhard Ørn Palsson

Research output: Contribution to journalReview articlepeer-review

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.

Original languageEnglish
Pages (from-to)842-859
Number of pages18
JournalCell Systems
Volume12
Issue number9
DOIs
Publication statusPublished - 1 Sept 2021

Bibliographical note

Funding Information: We thank Almut Heinken and Ines Thiele for providing us with the starting draft AGORA models and Marc Abrams for reviewing this manuscript. This work was supported by NIH grants U01 AI124316 and R01GM057089 and Novo Nordisk Foundation grant NNF10CC1016517. Y.S. designed the study, conducted computational analysis, and wrote the perspective; B.O.P. critically reviewed the content. The authors declare no competing interests. Funding Information: We thank Almut Heinken and Ines Thiele for providing us with the starting draft AGORA models and Marc Abrams for reviewing this manuscript. This work was supported by NIH grants U01 AI124316 and R01GM057089 and Novo Nordisk Foundation grant NNF10CC1016517 . Publisher Copyright: © 2021 The Authors

Other keywords

  • functional annotation
  • metabolic modeling
  • metabolic reconstructions
  • systems biology

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