Matching Hierarchical Structures Using Association Graphs
IEEE Transactions on Pattern Analysis and Machine Intelligence
RECOMB '04 Proceedings of the eighth annual international conference on Resaerch in computational molecular biology
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Finding protein functional modules in protein interaction networks amounts to finding densely connected subgraphs. Standard methods such as cliques and k-cores produce very small subgraphs due to highly sparse connections in most protein networks. Furthermore, standard methods are not applicable on weighted protein networks. We propose a method to identify cliques on weighted graphs. To overcome the sparsity problem, we introduce the concept of transitive closure on weighted graphs which is based on enforcing a transitive affinity inequality on the connection weights, and an algorithm to compute them. Using protein network from TAP-MS experiment on yeast, we discover a large number of cliques that are densely connected protein modules, with clear biological meanings as shown on Gene Ontology analysis.