4.1 Article

The Gene Ontology (GO) Cellular Component Ontology: integration with SAO (Subcellular Anatomy Ontology) and other recent developments

期刊

JOURNAL OF BIOMEDICAL SEMANTICS
卷 4, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/2041-1480-4-20

关键词

Gene ontology; Cellular component ontology; Subcellular anatomy ontology; Neuroscience; Annotation; Ontology language; Ontology integration; Neuroscience information framework

资金

  1. National Human Genome Research Institute (NHGRI) P41 grant [5P41HG002273-09]
  2. European Union RTD Programme 'Quality of Life and Management of Living Resources' [QLRI-CT-2001-00981, QLRI-CT-2001-00015]
  3. UniProtKB-GOA groups at EMBL-EBI
  4. National Institute of General Medical Sciences (NIGMS) [GM080646]
  5. European Molecular Biology Laboratory (EMBL)
  6. European Bioinformatics Institute Outstation (EMBL-EBI)
  7. NIH via the National Institute on Drug Abuse [HHSN271200800035C]
  8. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  9. [HG002273]

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Background: The Gene Ontology (GO) (http://www.geneontology.org/) contains a set of terms for describing the activity and actions of gene products across all kingdoms of life. Each of these activities is executed in a location within a cell or in the vicinity of a cell. In order to capture this context, the GO includes a sub-ontology called the Cellular Component (CC) ontology (GO-CCO). The primary use of this ontology is for GO annotation, but it has also been used for phenotype annotation, and for the annotation of images. Another ontology with similar scope to the GO-CCO is the Subcellular Anatomy Ontology (SAO), part of the Neuroscience Information Framework Standard (NIFSTD) suite of ontologies. The SAO also covers cell components, but in the domain of neuroscience. Description: Recently, the GO-CCO was enriched in content and links to the Biological Process and Molecular Function branches of GO as well as to other ontologies. This was achieved in several ways. We carried out an amalgamation of SAO terms with GO-CCO ones; as a result, nearly 100 new neuroscience-related terms were added to the GO. The GO-CCO also contains relationships to GO Biological Process and Molecular Function terms, as well as connecting to external ontologies such as the Cell Ontology (CL). Terms representing protein complexes in the Protein Ontology (PRO) reference GO-CCO terms for their species-generic counterparts. GO-CCO terms can also be used to search a variety of databases. Conclusions: In this publication we provide an overview of the GO-CCO, its overall design, and some recent extensions that make use of additional spatial information. One of the most recent developments of the GO-CCO was the merging in of the SAO, resulting in a single unified ontology designed to serve the needs of GO annotators as well as the specific needs of the neuroscience community.

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