Supporting the visual analysis of dynamic networks by clustering associated temporal attributes.

The visual analysis of dynamic networks is a challenging task. In this paper, we introduce a new approach supporting the discovery of substructures sharing a similar trend over time by combining computation, visualization and interaction. With existing techniques, their discovery would be a tedious endeavor because of the number of nodes, edges as well as time points to be compared. First, on the basis of the supergraph, we therefore group nodes and edges according to their associated attributes that are changing over time. Second, the supergraph is visualized to provide an overview of the groups of nodes and edges with similar behavior over time in terms of their associated attributes. Third, we provide specific interactions to explore and refine the temporal clustering, allowing the user to further steer the analysis of the dynamic network. We demonstrate our approach by the visual analysis of a large wireless mesh network.

The PluriNetWork: an electronic representation of the network underlying pluripotency in mouse, and its applications.

BACKGROUND: Analysis of the mechanisms underlying pluripotency and reprogramming would benefit substantially from easy access to an electronic network of genes, proteins and mechanisms. Moreover, interpreting gene expression data needs to move beyond just the identification of the up-/downregulation of key genes and of overrepresented processes and pathways, towards clarifying the essential effects of the experiment in molecular terms. METHODOLOGY/PRINCIPAL FINDINGS: We have assembled a network of 574 molecular interactions, stimulations and inhibitions, based on a collection of research data from 177 publications until June 2010, involving 274 mouse genes/proteins, all in a standard electronic format, enabling analyses by readily available software such as Cytoscape and its plugins. The network includes the core circuit of Oct4 (Pou5f1), Sox2 and Nanog, its periphery (such as Stat3, Klf4, Esrrb, and c-Myc), connections to upstream signaling pathways (such as Activin, WNT, FGF, BMP, Insulin, Notch and LIF), and epigenetic regulators as well as some other relevant genes/proteins, such as proteins involved in nuclear import/export. We describe the general properties of the network, as well as a Gene Ontology analysis of the genes included. We use several expression data sets to condense the network to a set of network links that are affected in the course of an experiment, yielding hypotheses about the underlying mechanisms. CONCLUSIONS/SIGNIFICANCE: We have initiated an electronic data repository that will be useful to understand pluripotency and to facilitate the interpretation of high-throughput data. To keep up with the growth of knowledge on the fundamental processes of pluripotency and reprogramming, we suggest to combine Wiki and social networking software towards a community curation system that is easy to use and flexible, and tailored to provide a benefit for the scientist, and to improve communication and exchange of research results. A PluriNetWork tutorial is available at http://www.ibima.med.uni-rostock.de/IBIMA/PluriNetWork/.