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The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability

BACKGROUND: The Cell Ontology (CL) is an OBO Foundry candidate ontology covering the domain of canonical, natural biological cell types. Since its inception in 2005, the CL has undergone multiple rounds of revision and expansion, most notably in its representation of hematopoietic cells. For in vivo...

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Autores principales: Diehl, Alexander D., Meehan, Terrence F., Bradford, Yvonne M., Brush, Matthew H., Dahdul, Wasila M., Dougall, David S., He, Yongqun, Osumi-Sutherland, David, Ruttenberg, Alan, Sarntivijai, Sirarat, Van Slyke, Ceri E., Vasilevsky, Nicole A., Haendel, Melissa A., Blake, Judith A., Mungall, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932724/
https://www.ncbi.nlm.nih.gov/pubmed/27377652
http://dx.doi.org/10.1186/s13326-016-0088-7
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author Diehl, Alexander D.
Meehan, Terrence F.
Bradford, Yvonne M.
Brush, Matthew H.
Dahdul, Wasila M.
Dougall, David S.
He, Yongqun
Osumi-Sutherland, David
Ruttenberg, Alan
Sarntivijai, Sirarat
Van Slyke, Ceri E.
Vasilevsky, Nicole A.
Haendel, Melissa A.
Blake, Judith A.
Mungall, Christopher J.
author_facet Diehl, Alexander D.
Meehan, Terrence F.
Bradford, Yvonne M.
Brush, Matthew H.
Dahdul, Wasila M.
Dougall, David S.
He, Yongqun
Osumi-Sutherland, David
Ruttenberg, Alan
Sarntivijai, Sirarat
Van Slyke, Ceri E.
Vasilevsky, Nicole A.
Haendel, Melissa A.
Blake, Judith A.
Mungall, Christopher J.
author_sort Diehl, Alexander D.
collection PubMed
description BACKGROUND: The Cell Ontology (CL) is an OBO Foundry candidate ontology covering the domain of canonical, natural biological cell types. Since its inception in 2005, the CL has undergone multiple rounds of revision and expansion, most notably in its representation of hematopoietic cells. For in vivo cells, the CL focuses on vertebrates but provides general classes that can be used for other metazoans, which can be subtyped in species-specific ontologies. CONSTRUCTION AND CONTENT: Recent work on the CL has focused on extending the representation of various cell types, and developing new modules in the CL itself, and in related ontologies in coordination with the CL. For example, the Kidney and Urinary Pathway Ontology was used as a template to populate the CL with additional cell types. In addition, subtypes of the class ‘cell in vitro’ have received improved definitions and labels to provide for modularity with the representation of cells in the Cell Line Ontology and Reagent Ontology. Recent changes in the ontology development methodology for CL include a switch from OBO to OWL for the primary encoding of the ontology, and an increasing reliance on logical definitions for improved reasoning. UTILITY AND DISCUSSION: The CL is now mandated as a metadata standard for large functional genomics and transcriptomics projects, and is used extensively for annotation, querying, and analyses of cell type specific data in sequencing consortia such as FANTOM5 and ENCODE, as well as for the NIAID ImmPort database and the Cell Image Library. The CL is also a vital component used in the modular construction of other biomedical ontologies—for example, the Gene Ontology and the cross-species anatomy ontology, Uberon, use CL to support the consistent representation of cell types across different levels of anatomical granularity, such as tissues and organs. CONCLUSIONS: The ongoing improvements to the CL make it a valuable resource to both the OBO Foundry community and the wider scientific community, and we continue to experience increased interest in the CL both among developers and within the user community.
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spelling pubmed-49327242016-07-06 The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability Diehl, Alexander D. Meehan, Terrence F. Bradford, Yvonne M. Brush, Matthew H. Dahdul, Wasila M. Dougall, David S. He, Yongqun Osumi-Sutherland, David Ruttenberg, Alan Sarntivijai, Sirarat Van Slyke, Ceri E. Vasilevsky, Nicole A. Haendel, Melissa A. Blake, Judith A. Mungall, Christopher J. J Biomed Semantics Database BACKGROUND: The Cell Ontology (CL) is an OBO Foundry candidate ontology covering the domain of canonical, natural biological cell types. Since its inception in 2005, the CL has undergone multiple rounds of revision and expansion, most notably in its representation of hematopoietic cells. For in vivo cells, the CL focuses on vertebrates but provides general classes that can be used for other metazoans, which can be subtyped in species-specific ontologies. CONSTRUCTION AND CONTENT: Recent work on the CL has focused on extending the representation of various cell types, and developing new modules in the CL itself, and in related ontologies in coordination with the CL. For example, the Kidney and Urinary Pathway Ontology was used as a template to populate the CL with additional cell types. In addition, subtypes of the class ‘cell in vitro’ have received improved definitions and labels to provide for modularity with the representation of cells in the Cell Line Ontology and Reagent Ontology. Recent changes in the ontology development methodology for CL include a switch from OBO to OWL for the primary encoding of the ontology, and an increasing reliance on logical definitions for improved reasoning. UTILITY AND DISCUSSION: The CL is now mandated as a metadata standard for large functional genomics and transcriptomics projects, and is used extensively for annotation, querying, and analyses of cell type specific data in sequencing consortia such as FANTOM5 and ENCODE, as well as for the NIAID ImmPort database and the Cell Image Library. The CL is also a vital component used in the modular construction of other biomedical ontologies—for example, the Gene Ontology and the cross-species anatomy ontology, Uberon, use CL to support the consistent representation of cell types across different levels of anatomical granularity, such as tissues and organs. CONCLUSIONS: The ongoing improvements to the CL make it a valuable resource to both the OBO Foundry community and the wider scientific community, and we continue to experience increased interest in the CL both among developers and within the user community. BioMed Central 2016-07-04 /pmc/articles/PMC4932724/ /pubmed/27377652 http://dx.doi.org/10.1186/s13326-016-0088-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Database
Diehl, Alexander D.
Meehan, Terrence F.
Bradford, Yvonne M.
Brush, Matthew H.
Dahdul, Wasila M.
Dougall, David S.
He, Yongqun
Osumi-Sutherland, David
Ruttenberg, Alan
Sarntivijai, Sirarat
Van Slyke, Ceri E.
Vasilevsky, Nicole A.
Haendel, Melissa A.
Blake, Judith A.
Mungall, Christopher J.
The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability
title The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability
title_full The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability
title_fullStr The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability
title_full_unstemmed The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability
title_short The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability
title_sort cell ontology 2016: enhanced content, modularization, and ontology interoperability
topic Database
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932724/
https://www.ncbi.nlm.nih.gov/pubmed/27377652
http://dx.doi.org/10.1186/s13326-016-0088-7
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