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PATIKA: An informatics infrastructure for cellular networks

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Ontology

Ontology

PATIKA: An informatics

infrastructure for cellular networks

Center for Bioinformatics and Computer Engineering Department, Bilkent University, Ankara 06800, Turkey

§Presenting authors †Corresponding author

C. Aksay, A. Ayaz, O. Babur§, C. Bilgin, A. Cetintas, A. Civril, R. Colak, G. Cozen, E. Demir§

U. Dogrusoz§, †, Z. Erson, O. Gerdaneri, E. Giral, G. Gulesir, G. Nisanci, O. Sakarya, H.Yildirim

B is transformed into B’ by activation of A. In the actual case there are two A homologs, three B homologs and three B’ homologs.

Multi-User Environment

Collaborative construction and concurrent modification issues are also addressed. While a user is working on a pathway locally, others might change its topology or properties in the database.

Checks for up-to-date status of graph objects result in each graph object being color-coded with respect to its status:

Blue: Up-to-date

Red: Out-of-date

Yellow: Local Green: Locally Modified

Automated Layout

Before layout (left) and after layout (right). Specialized algorithms for layout of cellular pathways produce aesthetically pleasing drawings.

THE PATIKA PROJECTaims to develop methods and software tools for effective analysis of complex biological data at a functional level, consisting of following work-packages: • Define an ontology for a comprehensive representation of cellular pathways.

• Develop software tools and construct an associated database using this ontology and provide an effective environment for pathway data integration, storage, access, visualization and analysis.

• Design methods for automatic population and annotation of the pathway database.

• Design methods for effective, advanced querying of the pathway database.

• Design methods for inferring pathway activity using temporal data such as gene expression data.

• Develop techniques for effective visualization of pathway and gene expression data.

States: different forms of Bioentities via chemical modification (acetylated protein), localization (cytoplasmic ion), aberration (mutant gene), homomerization (dimers), etc.

Transitions: changes that states undergo. Basics

Incomplete Information Since the data on cellular processes is incomplete, different levels of information may be available for certain events. On the left, it is unknown whether S4 activates either of two transitions. Homologies

We define an intuitive, comprehensive, uncomplicated representation of cellular networks.

Software

Software

Bioentities: actors of the cellular events;

genetic (e.g., DNAs, proteins), chemical (e.g., ions), or physical (e.g., heat). Bioentity Interactions: high level, imprecise relations: protein-protein interaction, transcriptional regulation or

generic. A client/server architecture to provide access to PATIKA database

through a state-of-the-art visual pathway editor has been implemented in pure JavaTM.

Gene Expression Analysis

Support for analysis of gene expression data including a pathway activity inference method using gene expression data has been implemented.

Please visit POSTER F-67 for details of PATIKA’s Microarray Data Analysis Facilities.

Previous Contributors

Many people have previously worked on the project, to whom we’d like to thank, including A. Gursoy, R. Cetin-Atalay, M. Ozturk, S. F. Akgul, B. Caskurlu, E.D. Ozkan, C. Gerede, A. Kocatas, E. Karakoc, O. Kurt, Z. Madak, E. Sahin, E. Senel, S. Onay, B. Ozmen Querying Advanced, graph theoretic queries may be performed through specialized GUIs, including queries by value or ID, neighborhood and shortest path querying. Molecular Complexes: Non-covalently bound clusters of molecules behaving as a single state.

Cellular compartments: part of the model.

Interactions: relations of states with transitions such as substrate, product, activator and inhibitor.

Inspector window: Edit and visualize object properties.

External links to other databases.

Overview window: Handy for large

graphs. Annotate state variables Automated Layout Bioentity view: high level imprecise relations Compartments are also visualized Compound graph structure allows visualizing complexes and abstractions Graph Editor functions: Save, load, undo, zoom, move …

Mechanistic view Detailed relations Multiple views: Different subgraphs at different level of abstractions

Distinct user interfaces for easier visual discrimination

Color schemas for data visualization of queries, microarray or custom user data.

Referanslar

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