92 research outputs found
Identifying protein complexes from interaction networks based on clique percolation and distance restriction
Background: Identification of protein complexes in large interaction networks is crucial to understand principles of cellular organization and predict protein functions, which is one of the most important issues in the post-genomic era. Each protein might be subordinate multiple protein complexes in the real protein-protein interaction networks.Identifying overlapping protein complexes from protein-protein interaction networks is a considerable research topic.
Result: As an effective algorithm in identifying overlapping module structures, clique percolation method (CPM) has a wide range of application in social networks and biological networks. However, the recognition accuracy of algorithm CPM is lowly. Furthermore, algorithm CPM is unfit to identifying protein complexes with meso-scale when it applied in protein-protein interaction networks. In this paper, we propose a new topological model by extending the definition of k-clique community of algorithm CPM and introduced distance restriction, and develop a novel algorithm called CP-DR based on the new topological model for identifying protein complexes. In this new algorithm, the protein complex size is restricted by distance constraint to conquer the shortcomings of algorithm CPM. The algorithm CP-DR is applied to the protein interaction network of Sacchromyces cerevisiae and identifies many well known complexes.
Conclusion: The proposed algorithm CP-DR based on clique percolation and distance restriction makes it possible to identify dense subgraphs in protein interaction networks, a large number of which correspond to known protein complexes. Compared to algorithm CPM, algorithm CP-DR has more outstanding performance
Detecting highly overlapping community structure by greedy clique expansion
In complex networks it is common for each node to belong to several
communities, implying a highly overlapping community structure. Recent advances
in benchmarking indicate that existing community assignment algorithms that are
capable of detecting overlapping communities perform well only when the extent
of community overlap is kept to modest levels. To overcome this limitation, we
introduce a new community assignment algorithm called Greedy Clique Expansion
(GCE). The algorithm identifies distinct cliques as seeds and expands these
seeds by greedily optimizing a local fitness function. We perform extensive
benchmarks on synthetic data to demonstrate that GCE's good performance is
robust across diverse graph topologies. Significantly, GCE is the only
algorithm to perform well on these synthetic graphs, in which every node
belongs to multiple communities. Furthermore, when put to the task of
identifying functional modules in protein interaction data, and college dorm
assignments in Facebook friendship data, we find that GCE performs
competitively.Comment: 10 pages, 7 Figures. Implementation source and binaries available at
http://sites.google.com/site/greedycliqueexpansion
Communities in Networks
We survey some of the concepts, methods, and applications of community
detection, which has become an increasingly important area of network science.
To help ease newcomers into the field, we provide a guide to available
methodology and open problems, and discuss why scientists from diverse
backgrounds are interested in these problems. As a running theme, we emphasize
the connections of community detection to problems in statistical physics and
computational optimization.Comment: survey/review article on community structure in networks; published
version is available at
http://people.maths.ox.ac.uk/~porterm/papers/comnotices.pd
Recent advances in clustering methods for protein interaction networks
The increasing availability of large-scale protein-protein interaction data has made it possible to understand the basic components and organization of cell machinery from the network level. The arising challenge is how to analyze such complex interacting data to reveal the principles of cellular organization, processes and functions. Many studies have shown that clustering protein interaction network is an effective approach for identifying protein complexes or functional modules, which has become a major research topic in systems biology. In this review, recent advances in clustering methods for protein interaction networks will be presented in detail. The predictions of protein functions and interactions based on modules will be covered. Finally, the performance of different clustering methods will be compared and the directions for future research will be discussed
Community landscapes: an integrative approach to determine overlapping network module hierarchy, identify key nodes and predict network dynamics
Background: Network communities help the functional organization and
evolution of complex networks. However, the development of a method, which is
both fast and accurate, provides modular overlaps and partitions of a
heterogeneous network, has proven to be rather difficult. Methodology/Principal
Findings: Here we introduce the novel concept of ModuLand, an integrative
method family determining overlapping network modules as hills of an influence
function-based, centrality-type community landscape, and including several
widely used modularization methods as special cases. As various adaptations of
the method family, we developed several algorithms, which provide an efficient
analysis of weighted and directed networks, and (1) determine pervasively
overlapping modules with high resolution; (2) uncover a detailed hierarchical
network structure allowing an efficient, zoom-in analysis of large networks;
(3) allow the determination of key network nodes and (4) help to predict
network dynamics. Conclusions/Significance: The concept opens a wide range of
possibilities to develop new approaches and applications including network
routing, classification, comparison and prediction.Comment: 25 pages with 6 figures and a Glossary + Supporting Information
containing pseudo-codes of all algorithms used, 14 Figures, 5 Tables (with 18
module definitions, 129 different modularization methods, 13 module
comparision methods) and 396 references. All algorithms can be downloaded
from this web-site: http://www.linkgroup.hu/modules.ph
Multiple Alignment of Protein Interaction Networks by Three-Index Assignment Algorithm
Bio-molecular networks have led to many discoveries in molecular biology. The most atypical of them are protein-protein interaction (PPI) networks. In PPI networks the nodes refer to proteins and edges refer to interactions between nodes. The comparison of PPI networks can be demonstrated as a powerful approach for examining interactions in these networks and predicting protein functions. This thesis contributes a new alignment algorithm for aligning three PPI networks. We examine how Three-Index Assignment Problem via Hungarian Pair Matching algorithm is used to maximize the complete match between the three networks to identify protein triplets with higher similarity. We have performed tests on PPI networks extracted from the IntAct database and IsoRank database. We experimentally show that the results obtained by our method have more biological significance in comparison to other methods and can be used in future to predict protein functions and complexes in PPI networks
Clustering and Community Detection in Directed Networks: A Survey
Networks (or graphs) appear as dominant structures in diverse domains,
including sociology, biology, neuroscience and computer science. In most of the
aforementioned cases graphs are directed - in the sense that there is
directionality on the edges, making the semantics of the edges non symmetric.
An interesting feature that real networks present is the clustering or
community structure property, under which the graph topology is organized into
modules commonly called communities or clusters. The essence here is that nodes
of the same community are highly similar while on the contrary, nodes across
communities present low similarity. Revealing the underlying community
structure of directed complex networks has become a crucial and
interdisciplinary topic with a plethora of applications. Therefore, naturally
there is a recent wealth of research production in the area of mining directed
graphs - with clustering being the primary method and tool for community
detection and evaluation. The goal of this paper is to offer an in-depth review
of the methods presented so far for clustering directed networks along with the
relevant necessary methodological background and also related applications. The
survey commences by offering a concise review of the fundamental concepts and
methodological base on which graph clustering algorithms capitalize on. Then we
present the relevant work along two orthogonal classifications. The first one
is mostly concerned with the methodological principles of the clustering
algorithms, while the second one approaches the methods from the viewpoint
regarding the properties of a good cluster in a directed network. Further, we
present methods and metrics for evaluating graph clustering results,
demonstrate interesting application domains and provide promising future
research directions.Comment: 86 pages, 17 figures. Physics Reports Journal (To Appear
Module detection in complex networks using integer optimisation
<p>Abstract</p> <p>Background</p> <p>The detection of <it>modules or community structure </it>is widely used to reveal the underlying properties of complex networks in biology, as well as physical and social sciences. Since the adoption of modularity as a measure of network topological properties, several methodologies for the discovery of community structure based on modularity maximisation have been developed. However, satisfactory partitions of large graphs with modest computational resources are particularly challenging due to the NP-hard nature of the related optimisation problem. Furthermore, it has been suggested that optimising the modularity metric can reach a resolution limit whereby the algorithm fails to detect smaller communities than a specific size in large networks.</p> <p>Results</p> <p>We present a novel solution approach to identify community structure in large complex networks and address resolution limitations in module detection. The proposed algorithm employs modularity to express network community structure and it is based on mixed integer optimisation models. The solution procedure is extended through an iterative procedure to diminish effects that tend to agglomerate smaller modules (resolution limitations).</p> <p>Conclusions</p> <p>A comprehensive comparative analysis of methodologies for module detection based on modularity maximisation shows that our approach outperforms previously reported methods. Furthermore, in contrast to previous reports, we propose a strategy to handle resolution limitations in modularity maximisation. Overall, we illustrate ways to improve existing methodologies for community structure identification so as to increase its efficiency and applicability.</p
A least square method based model for identifying protein complexes in protein-protein interaction network
Protein complex formed by a group of physical interacting proteins plays a crucial role in cell activities. Great effort has been made to computationally identify protein complexes from protein-protein interaction (PPI) network. However, the accuracy of the prediction is still far from being satisfactory, because the topological structures of protein complexes in the PPI network are too complicated. This paper proposes a novel optimization framework to detect complexes from PPI network, named PLSMC. The method is on the basis of the fact that if two proteins are in a common complex, they are likely to be interacting. PLSMC employs this relation to determine complexes by a penalized least squares method. PLSMC is applied to several public yeast PPI networks, and compared with several state-of-the-art methods. The results indicate that PLSMC outperforms other methods. In particular, complexes predicted by PLSMC can match known complexes with a higher accuracy than other methods. Furthermore, the predicted complexes have high functional homogeneity
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