Evidence map›Paper›PMID 22589706›Full record

ArticlePLoS computational biology2012

NIBBS-search for fast and accurate prediction of phenotype-biased metabolic systems.

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

Abstract read
In one paragraph

Article in PLoS computational biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Matthew C SchmidtDepartment of Computer Science, North Carolina State University, Raleigh, North Carolina, United States of America.
Andrea M Rocha
Kanchana Padmanabhan
Yekaterina Shpanskaya
Jill Banfield
Kathleen Scott
James R Mihelcic
Nagiza F Samatova

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Databases, ProteinModels, BiologicalAlgorithmsAnimalsComputer SimulationData MiningHumansMetabolomePeriodicals as TopicPhenotypeProtein Interaction MappingProteomeSignal TransductionProteome

Identifiers

PMID22589706
PMCPMC3349732

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.