AI Article Synopsis

  • Genome-scale metabolic networks and transcriptomic data are essential for understanding an organism's metabolism, but integrating them effectively is difficult.
  • This study introduces a method called metaboGSE, which constructs condition-specific metabolic sub-networks by strategically removing genes based on transcriptomic data, and evaluates them using a fitness function.
  • The method is validated using public data for Yarrowia lipolytica and mice, showing that it yields more specific gene ontology terms than traditional gene set enrichment methods such as GSEA or topGO.
  • The metaboGSE R package is available for researchers at a provided link.

Article Abstract

Motivation: Genome-scale metabolic networks and transcriptomic data represent complementary sources of knowledge about an organism's metabolism, yet their integration to achieve biological insight remains challenging.

Results: We investigate here condition-specific series of metabolic sub-networks constructed by successively removing genes from a comprehensive network. The optimal order of gene removal is deduced from transcriptomic data. The sub-networks are evaluated via a fitness function, which estimates their degree of alteration. We then consider how a gene set, i.e. a group of genes contributing to a common biological function, is depleted in different series of sub-networks to detect the difference between experimental conditions. The method, named metaboGSE, is validated on public data for Yarrowia lipolytica and mouse. It is shown to produce GO terms of higher specificity compared to popular gene set enrichment methods like GSEA or topGO.

Availability And Implementation: The metaboGSE R package is available at https://CRAN.R-project.org/package=metaboGSE.

Supplementary Information: Supplementary data are available at Bioinformatics online.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596900PMC
http://dx.doi.org/10.1093/bioinformatics/bty929DOI Listing

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