An improved ontological representation of dendritic cells as a paradigm for all cell types.

Published

Journal Article

Recent increases in the volume and diversity of life science data and information and an increasing emphasis on data sharing and interoperability have resulted in the creation of a large number of biological ontologies, including the Cell Ontology (CL), designed to provide a standardized representation of cell types for data annotation. Ontologies have been shown to have significant benefits for computational analyses of large data sets and for automated reasoning applications, leading to organized attempts to improve the structure and formal rigor of ontologies to better support computation. Currently, the CL employs multiple is_a relations, defining cell types in terms of histological, functional, and lineage properties, and the majority of definitions are written with sufficient generality to hold across multiple species. This approach limits the CL's utility for computation and for cross-species data integration.To enhance the CL's utility for computational analyses, we developed a method for the ontological representation of cells and applied this method to develop a dendritic cell ontology (DC-CL). DC-CL subtypes are delineated on the basis of surface protein expression, systematically including both species-general and species-specific types and optimizing DC-CL for the analysis of flow cytometry data. We avoid multiple uses of is_a by linking DC-CL terms to terms in other ontologies via additional, formally defined relations such as has_function.This approach brings benefits in the form of increased accuracy, support for reasoning, and interoperability with other ontology resources. Accordingly, we propose our method as a general strategy for the ontological representation of cells. DC-CL is available from http://www.obofoundry.org.

Full Text

Cited Authors

  • Masci, AM; Arighi, CN; Diehl, AD; Lieberman, AE; Mungall, C; Scheuermann, RH; Smith, B; Cowell, LG

Published Date

  • February 25, 2009

Published In

Volume / Issue

  • 10 /

Start / End Page

  • 70 -

PubMed ID

  • 19243617

Pubmed Central ID

  • 19243617

Electronic International Standard Serial Number (EISSN)

  • 1471-2105

International Standard Serial Number (ISSN)

  • 1471-2105

Digital Object Identifier (DOI)

  • 10.1186/1471-2105-10-70

Language

  • eng