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NIBBS-Search for Fast and Accurate Prediction of Phenotype-Biased Metabolic Systems

Overview of attention for article published in PLoS Computational Biology, May 2012
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Title
NIBBS-Search for Fast and Accurate Prediction of Phenotype-Biased Metabolic Systems
Published in
PLoS Computational Biology, May 2012
DOI 10.1371/journal.pcbi.1002490
Pubmed ID
Authors

Matthew C. Schmidt, Andrea M. Rocha, Kanchana Padmanabhan, Yekaterina Shpanskaya, Jill Banfield, Kathleen Scott, James R. Mihelcic, Nagiza F. Samatova

Abstract

Understanding of genotype-phenotype associations is important not only for furthering our knowledge on internal cellular processes, but also essential for providing the foundation necessary for genetic engineering of microorganisms for industrial use (e.g., production of bioenergy or biofuels). However, genotype-phenotype associations alone do not provide enough information to alter an organism's genome to either suppress or exhibit a phenotype. It is important to look at the phenotype-related genes in the context of the genome-scale network to understand how the genes interact with other genes in the organism. Identification of metabolic subsystems involved in the expression of the phenotype is one way of placing the phenotype-related genes in the context of the entire network. A metabolic system refers to a metabolic network subgraph; nodes are compounds and edges labels are the enzymes that catalyze the reaction. The metabolic subsystem could be part of a single metabolic pathway or span parts of multiple pathways. Arguably, comparative genome-scale metabolic network analysis is a promising strategy to identify these phenotype-related metabolic subsystems. Network Instance-Based Biased Subgraph Search (NIBBS) is a graph-theoretic method for genome-scale metabolic network comparative analysis that can identify metabolic systems that are statistically biased toward phenotype-expressing organismal networks. We set up experiments with target phenotypes like hydrogen production, TCA expression, and acid-tolerance. We show via extensive literature search that some of the resulting metabolic subsystems are indeed phenotype-related and formulate hypotheses for other systems in terms of their role in phenotype expression. NIBBS is also orders of magnitude faster than MULE, one of the most efficient maximal frequent subgraph mining algorithms that could be adjusted for this problem. Also, the set of phenotype-biased metabolic systems output by NIBBS comes very close to the set of phenotype-biased subgraphs output by an exact maximally-biased subgraph enumeration algorithm ( MBS-Enum ). The code (NIBBS and the module to visualize the identified subsystems) is available at http://freescience.org/cs/NIBBS.

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Geographical breakdown

Country Count As %
United States 3 7%
New Zealand 1 2%
South Africa 1 2%
Brazil 1 2%
Unknown 36 86%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 13 31%
Researcher 10 24%
Other 3 7%
Student > Master 3 7%
Professor 3 7%
Other 6 14%
Unknown 4 10%
Readers by discipline Count As %
Agricultural and Biological Sciences 18 43%
Computer Science 7 17%
Biochemistry, Genetics and Molecular Biology 6 14%
Environmental Science 3 7%
Engineering 2 5%
Other 0 0%
Unknown 6 14%