ArticlePloS one2010
Module discovery by exhaustive search for densely connected, co-expressed regions in biomolecular interaction networks.
Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Biclustering data analysis: a comprehensive survey.Briefings in bioinformatics · 2024Review
- BicNET: Flexible module discovery in large-scale biological networks using biclustering.Algorithms for molecular biology : AMB · 2016Article
- Quantitative assessment of gene expression network module-validation methods.Scientific reports · 2015Article
- Understanding and predicting binding between human leukocyte antigens (HLAs) and peptides by network analysis.BMC bioinformatics · 2015Article
- Integrative approaches for finding modular structure in biological networks.Nature reviews. Genetics · 2013Review
- Computational solutions for omics data.Nature reviews. Genetics · 2013Review
- Systems genetics in "-omics" era: current and future development.Theory in biosciences = Theorie in den Biowissenschaften · 2013Review
- Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response.PloS one · 2013Article
- Identifying grade/stage-related active modules in human co-regulatory networks: a case study for breast cancer.Omics : a journal of integrative biology · 2012Article
- Inferring cancer subnetwork markers using density-constrained biclustering.Bioinformatics (Oxford, England) · 2010Article
Corrections and comments
- Erratum issued
Authors and funding
6 authors.
Funding
Abstract
backgroundComputational prediction of functionally related groups of genes (functional modules) from large-scale data is an important issue in computational biology. Gene expression experiments and interaction networks are well studied large-scale data sources, available for many not yet exhaustively annotated organisms. It has been well established, when analyzing these two data sources jointly, modules are often reflected by highly interconnected (dense) regions in the interaction networks whose participating genes are co-expressed. However, the tractability of the problem had remained unclear and methods by which to exhaustively search for such constellations had not been presented. METHODOLOGY/PRINCIPAL
findingsWe provide an algorithmic framework, referred to as Densely Connected Biclustering (DECOB), by which the aforementioned search problem becomes tractable. To benchmark the predictive power inherent to the approach, we computed all co-expressed, dense regions in physical protein and genetic interaction networks from human and yeast. An automatized filtering procedure reduces our output which results in smaller collections of modules, comparable to state-of-the-art approaches. Our results performed favorably in a fair benchmarking competition which adheres to standard criteria. We demonstrate the usefulness of an exhaustive module search, by using the unreduced output to more quickly perform GO term related function prediction tasks. We point out the advantages of our exhaustive output by predicting functional relationships using two examples. CONCLUSION/SIGNIFICANCE: We demonstrate that the computation of all densely connected and co-expressed regions in interaction networks is an approach to module discovery of considerable value. Beyond confirming the well settled hypothesis that such co-expressed, densely connected interaction network regions reflect functional modules, we open up novel computational ways to comprehensively analyze the modular organization of an organism based on prevalent and largely available large-scale datasets. AVAILABILITY: Software and data sets are available at http://www.sfu.ca/~ester/software/DECOB.zip.
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