Evidence map›Paper›PMID 17650343›Full record

ArticleBMC bioinformatics2007

Semantic integration to identify overlapping functional modules in protein interaction networks.

Young-Rae Cho, Woochang Hwang, Murali Ramanathan, Aidong Zhang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

44 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Young-Rae ChoDepartment of Computer Science and Engineering, State University of New York, Buffalo, NY, USA. ycho8@cse.buffalo.edu
Woochang Hwang
Murali Ramanathan
Aidong Zhang

Funding

Computational Approaches to Disease Causes and TreatmentP20GM067650 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ZHANG, AIDONG · 2003 to 2005
$1.2M
NIGMS NIH HHS 1 P20 GM067650-01A1NIGMS NIH HHS P20 GM067650
6 · The paper itself

Abstract

backgroundThe systematic analysis of protein-protein interactions can enable a better understanding of cellular organization, processes and functions. Functional modules can be identified from the protein interaction networks derived from experimental data sets. However, these analyses are challenging because of the presence of unreliable interactions and the complex connectivity of the network. The integration of protein-protein interactions with the data from other sources can be leveraged for improving the effectiveness of functional module detection algorithms.

resultsWe have developed novel metrics, called semantic similarity and semantic interactivity, which use Gene Ontology (GO) annotations to measure the reliability of protein-protein interactions. The protein interaction networks can be converted into a weighted graph representation by assigning the reliability values to each interaction as a weight. We presented a flow-based modularization algorithm to efficiently identify overlapping modules in the weighted interaction networks. The experimental results show that the semantic similarity and semantic interactivity of interacting pairs were positively correlated with functional co-occurrence. The effectiveness of the algorithm for identifying modules was evaluated using functional categories from the MIPS database. We demonstrated that our algorithm had higher accuracy compared to other competing approaches.

conclusionThe integration of protein interaction networks with GO annotation data and the capability of detecting overlapping modules substantially improve the accuracy of module identification.

Indexed as

Databases, ProteinModels, BiologicalNatural Language ProcessingAlgorithmsComputer SimulationInformation Storage and RetrievalProtein Interaction MappingProteomeSemanticsSignal TransductionSystems IntegrationProteome

Identifiers

PMID17650343
PMCPMC1971074

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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.