| Literature DB >> 24099179 |
Inna Kuperstein1, David P A Cohen, Stuart Pook, Eric Viara, Laurence Calzone, Emmanuel Barillot, Andrei Zinovyev.
Abstract
BACKGROUND: Molecular biology knowledge can be formalized and systematically represented in a computer-readable form as a comprehensive map of molecular interactions. There exist an increasing number of maps of molecular interactions containing detailed and step-wise description of various cell mechanisms. It is difficult to explore these large maps, to organize discussion of their content and to maintain them. Several efforts were recently made to combine these capabilities together in one environment, and NaviCell is one of them.Entities:
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Year: 2013 PMID: 24099179 PMCID: PMC3851986 DOI: 10.1186/1752-0509-7-100
Source DB: PubMed Journal: BMC Syst Biol ISSN: 1752-0509
Comparison of NaviCell features with existing tools
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*Analytical tools:
Pathway projector-Data mapping, Path search, Sequence-based search (BLAST), Pathway prediction; KEGG-Data mapping, Pathways enrichment analysis; Reactome-Data mapping, Pathways enrichment analysis, Path search; CellDesigner-Simulation; Payao-analytical text-mining by PathText; SBGN-ED-Data mapping, Network analysis, Simulation; Panther-Data mapping; BioCyc-Pathway Tools Software; PathVisio-Data mapping, Pathways enrichment analysis; GenMAPP-Data mapping, Pathways enrichment analysis; BioUML-Simulation and analysis; Cytoscape-Various tools available through plugins.
Figure 1General architecture of NaviCell environment.
Figure 2NaviCell layout. (A) Map panel with top-level view of the modular RB-E2F map, (B) Fragment of the detailed view of the map with a callout and markers, (C) Selection panel with list of the map entities grouped per type.
Figure 3NaviCell semantic zooming. The same area of the map is visualized at four different zoom levels; each image is twice smaller than in the preceding zoom level. (A) In the top-level view, boundaries of map modules are visualized, (B) In the pruned view, only the most important molecular cascades are visualized, (C) In the hidden details view, unreadable details (such as residue names) are hidden, (D) In the detailed view, entity names, modifications and reaction IDs are visible.
Figure 4Module maps. (A) RB module on the Top-level view zoom, (B) RB module on the hidden-details view zoom, (C) RB module shown as a separate map.
Figure 5Annotation post in the blog for the complex CDK2:cyclin A2*:p27Kip1*.