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Using ontologies to study cell transitions
BACKGROUND: Understanding, modelling and influencing the transition between different states of cells, be it reprogramming of somatic cells to pluripotency or trans-differentiation between cells, is a hot topic in current biomedical and cell-biological research. Nevertheless, the large body of publi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128511/ https://www.ncbi.nlm.nih.gov/pubmed/24103098 http://dx.doi.org/10.1186/2041-1480-4-25 |
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author | Fuellen, Georg Jansen, Ludger Leser, Ulf Kurtz, Andreas |
author_facet | Fuellen, Georg Jansen, Ludger Leser, Ulf Kurtz, Andreas |
author_sort | Fuellen, Georg |
collection | PubMed |
description | BACKGROUND: Understanding, modelling and influencing the transition between different states of cells, be it reprogramming of somatic cells to pluripotency or trans-differentiation between cells, is a hot topic in current biomedical and cell-biological research. Nevertheless, the large body of published knowledge in this area is underused, as most results are only represented in natural language, impeding their finding, comparison, aggregation, and usage. Scientific understanding of the complex molecular mechanisms underlying cell transitions could be improved by making essential pieces of knowledge available in a formal (and thus computable) manner. RESULTS: We describe the outline of two ontologies for cell phenotypes and for cellular mechanisms which together enable the representation of data curated from the literature or obtained by bioinformatics analyses and thus for building a knowledge base on mechanisms involved in cellular reprogramming. In particular, we discuss how comprehensive ontologies of cell phenotypes and of changes in mechanisms can be designed using the entity-quality (EQ) model. CONCLUSIONS: We show that the principles for building cellular ontologies published in this work allow deeper insights into the relations between the continuants (cell phenotypes) and the occurrents (cell mechanism changes) involved in cellular reprogramming, although implementation remains for future work. Further, our design principles lead to ontologies that allow the meaningful application of similarity searches in the spaces of cell phenotypes and of mechanisms, and, especially, of changes of mechanisms during cellular transitions. |
format | Online Article Text |
id | pubmed-4128511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41285112014-08-12 Using ontologies to study cell transitions Fuellen, Georg Jansen, Ludger Leser, Ulf Kurtz, Andreas J Biomed Semantics Research BACKGROUND: Understanding, modelling and influencing the transition between different states of cells, be it reprogramming of somatic cells to pluripotency or trans-differentiation between cells, is a hot topic in current biomedical and cell-biological research. Nevertheless, the large body of published knowledge in this area is underused, as most results are only represented in natural language, impeding their finding, comparison, aggregation, and usage. Scientific understanding of the complex molecular mechanisms underlying cell transitions could be improved by making essential pieces of knowledge available in a formal (and thus computable) manner. RESULTS: We describe the outline of two ontologies for cell phenotypes and for cellular mechanisms which together enable the representation of data curated from the literature or obtained by bioinformatics analyses and thus for building a knowledge base on mechanisms involved in cellular reprogramming. In particular, we discuss how comprehensive ontologies of cell phenotypes and of changes in mechanisms can be designed using the entity-quality (EQ) model. CONCLUSIONS: We show that the principles for building cellular ontologies published in this work allow deeper insights into the relations between the continuants (cell phenotypes) and the occurrents (cell mechanism changes) involved in cellular reprogramming, although implementation remains for future work. Further, our design principles lead to ontologies that allow the meaningful application of similarity searches in the spaces of cell phenotypes and of mechanisms, and, especially, of changes of mechanisms during cellular transitions. BioMed Central 2013-10-08 /pmc/articles/PMC4128511/ /pubmed/24103098 http://dx.doi.org/10.1186/2041-1480-4-25 Text en Copyright © 2013 Fuellen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fuellen, Georg Jansen, Ludger Leser, Ulf Kurtz, Andreas Using ontologies to study cell transitions |
title | Using ontologies to study cell transitions |
title_full | Using ontologies to study cell transitions |
title_fullStr | Using ontologies to study cell transitions |
title_full_unstemmed | Using ontologies to study cell transitions |
title_short | Using ontologies to study cell transitions |
title_sort | using ontologies to study cell transitions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128511/ https://www.ncbi.nlm.nih.gov/pubmed/24103098 http://dx.doi.org/10.1186/2041-1480-4-25 |
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