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We are analyzing https://link.springer.com/article/10.1186/1471-2105-12-6.

Title:
Logical Development of the Cell Ontology | BMC Bioinformatics
Description:
Background The Cell Ontology (CL) is an ontology for the representation of in vivo cell types. As biological ontologies such as the CL grow in complexity, they become increasingly difficult to use and maintain. By making the information in the ontology computable, we can use automated reasoners to detect errors and assist with classification. Here we report on the generation of computable definitions for the hematopoietic cell types in the CL. Results Computable definitions for over 340 CL classes have been created using a genus-differentia approach. These define cell types according to multiple axes of classification such as the protein complexes found on the surface of a cell type, the biological processes participated in by a cell type, or the phenotypic characteristics associated with a cell type. We employed automated reasoners to verify the ontology and to reveal mistakes in manual curation. The implementation of this process exposed areas in the ontology where new cell type classes were needed to accommodate species-specific expression of cellular markers. Our use of reasoners also inferred new relationships within the CL, and between the CL and the contributing ontologies. This restructured ontology can be used to identify immune cells by flow cytometry, supports sophisticated biological queries involving cells, and helps generate new hypotheses about cell function based on similarities to other cell types. Conclusion Use of computable definitions enhances the development of the CL and supports the interoperability of OBO ontologies.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Telecommunications
  • Education
  • Science

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We don't see any clear sign of profit-making.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com might be cashing in, but we can't detect the method they're using.

Keywords {πŸ”}

cell, ontology, types, computable, definitions, classes, cells, ontologies, relationships, class, pubmed, article, type, figure, hematopoietic, isa, google, scholar, obo, defined, inferred, surface, protein, relationship, reasoners, markers, reasoner, biological, expression, owl, cas, masci, automated, natural, central, developsfrom, mature, gene, hemocl, oboedit, alphabeta, definition, capableof, authors, immune, hierarchy, complex, killer, receptor, mungall,

Topics {βœ’οΈ}

net/viewvc/obo/obo/ontology/anatomy/cell_type anna maria masci gov/pubmed/20123131 http article download pdf medicine-clinical terms entity/quality-based logical definitions 2nd international conference mhc-ib protein complexes author information authors view held human-oriented textual definitions testing neural-immune interactions accommodate species-specific expression b-cell immunological synapse lymphocyte receptor complex species-specific cell types reflect species-specific differences cell receptor complex related subjects species-neutral cell type hidden cell-classes displaying obo-edit software tools owl-indexed knowledge bases formal textual definitions represent species-specific expression red zig-zag hematopoietic stem cell central nervous system human stem cells double-positive thymocyte class cd11b-negative dendritic cell varying standards snomed-ct ontology-based phenotype annotation amm contributed terms privacy choices/manage cookies hematopoietic stem cells full size image de la salle de-ac02-05ch11231 natural t-regulatory cell nucleate erythrocyte cell receptor genes species-specific differences human skeletal phenome authors’ original file uber anatomy ontology gene ontology consortium human cell markers complex biomedical ontologies

Questions {❓}

  • Curotto de Lafaille MA, Lafaille JJ: Natural and adaptive foxp3+ regulatory T cells: more of the same or a division of labor?
  • Godfrey DI, MacDonald HR, Kronenberg M, Smyth MJ, Van Kaer L: NKT cells: what's in a name?

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Logical Development of the Cell Ontology
         description:The Cell Ontology (CL) is an ontology for the representation of in vivo cell types. As biological ontologies such as the CL grow in complexity, they become increasingly difficult to use and maintain. By making the information in the ontology computable, we can use automated reasoners to detect errors and assist with classification. Here we report on the generation of computable definitions for the hematopoietic cell types in the CL. Computable definitions for over 340 CL classes have been created using a genus-differentia approach. These define cell types according to multiple axes of classification such as the protein complexes found on the surface of a cell type, the biological processes participated in by a cell type, or the phenotypic characteristics associated with a cell type. We employed automated reasoners to verify the ontology and to reveal mistakes in manual curation. The implementation of this process exposed areas in the ontology where new cell type classes were needed to accommodate species-specific expression of cellular markers. Our use of reasoners also inferred new relationships within the CL, and between the CL and the contributing ontologies. This restructured ontology can be used to identify immune cells by flow cytometry, supports sophisticated biological queries involving cells, and helps generate new hypotheses about cell function based on similarities to other cell types. Use of computable definitions enhances the development of the CL and supports the interoperability of OBO ontologies.
         datePublished:2011-01-05T00:00:00Z
         dateModified:2011-01-05T00:00:00Z
         pageStart:1
         pageEnd:12
         license:http://creativecommons.org/licenses/by/2.0
         sameAs:https://doi.org/10.1186/1471-2105-12-6
         keywords:
            Gene Ontology
            Automate Reasoner
            Human Hematopoietic Stem Cell
            Nucleate Erythrocyte
            Cell Receptor Complex
            Bioinformatics
            Microarrays
            Computational Biology/Bioinformatics
            Computer Appl. in Life Sciences
            Algorithms
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                     address:
                        name:Department of Neurology, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, USA
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ScholarlyArticle:
      headline:Logical Development of the Cell Ontology
      description:The Cell Ontology (CL) is an ontology for the representation of in vivo cell types. As biological ontologies such as the CL grow in complexity, they become increasingly difficult to use and maintain. By making the information in the ontology computable, we can use automated reasoners to detect errors and assist with classification. Here we report on the generation of computable definitions for the hematopoietic cell types in the CL. Computable definitions for over 340 CL classes have been created using a genus-differentia approach. These define cell types according to multiple axes of classification such as the protein complexes found on the surface of a cell type, the biological processes participated in by a cell type, or the phenotypic characteristics associated with a cell type. We employed automated reasoners to verify the ontology and to reveal mistakes in manual curation. The implementation of this process exposed areas in the ontology where new cell type classes were needed to accommodate species-specific expression of cellular markers. Our use of reasoners also inferred new relationships within the CL, and between the CL and the contributing ontologies. This restructured ontology can be used to identify immune cells by flow cytometry, supports sophisticated biological queries involving cells, and helps generate new hypotheses about cell function based on similarities to other cell types. Use of computable definitions enhances the development of the CL and supports the interoperability of OBO ontologies.
      datePublished:2011-01-05T00:00:00Z
      dateModified:2011-01-05T00:00:00Z
      pageStart:1
      pageEnd:12
      license:http://creativecommons.org/licenses/by/2.0
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         Gene Ontology
         Automate Reasoner
         Human Hematopoietic Stem Cell
         Nucleate Erythrocyte
         Cell Receptor Complex
         Bioinformatics
         Microarrays
         Computational Biology/Bioinformatics
         Computer Appl. in Life Sciences
         Algorithms
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      author:
            name:Terrence F Meehan
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            name:Lindsay G Cowell
            affiliation:
                  name:Duke University Medical Center
                  address:
                     name:Dept. of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Judith A Blake
            affiliation:
                  name:The Jackson Laboratory
                  address:
                     name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Christopher J Mungall
            affiliation:
                  name:Lawrence Berkeley National Laboratory
                  address:
                     name:Lawrence Berkeley National Laboratory, Berkeley, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Alexander D Diehl
            affiliation:
                  name:The Jackson Laboratory
                  address:
                     name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
                     type:PostalAddress
                  type:Organization
                  name:University at Buffalo School of Medicine and Biomedical Sciences
                  address:
                     name:Department of Neurology, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, USA
                     type:PostalAddress
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         name:Lawrence Berkeley National Laboratory, Berkeley, USA
         type:PostalAddress
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      address:
         name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
         type:PostalAddress
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         name:Department of Neurology, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, USA
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Person:
      name:Terrence F Meehan
      affiliation:
            name:The Jackson Laboratory
            address:
               name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Anna Maria Masci
      affiliation:
            name:Duke University Medical Center
            address:
               name:Dept. of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, USA
               type:PostalAddress
            type:Organization
      name:Amina Abdulla
      affiliation:
            name:Lawrence Berkeley National Laboratory
            address:
               name:Lawrence Berkeley National Laboratory, Berkeley, USA
               type:PostalAddress
            type:Organization
      name:Lindsay G Cowell
      affiliation:
            name:Duke University Medical Center
            address:
               name:Dept. of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, USA
               type:PostalAddress
            type:Organization
      name:Judith A Blake
      affiliation:
            name:The Jackson Laboratory
            address:
               name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
               type:PostalAddress
            type:Organization
      name:Christopher J Mungall
      affiliation:
            name:Lawrence Berkeley National Laboratory
            address:
               name:Lawrence Berkeley National Laboratory, Berkeley, USA
               type:PostalAddress
            type:Organization
      name:Alexander D Diehl
      affiliation:
            name:The Jackson Laboratory
            address:
               name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
               type:PostalAddress
            type:Organization
            name:University at Buffalo School of Medicine and Biomedical Sciences
            address:
               name:Department of Neurology, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
      name:Dept. of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, USA
      name:Lawrence Berkeley National Laboratory, Berkeley, USA
      name:Dept. of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, USA
      name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
      name:Lawrence Berkeley National Laboratory, Berkeley, USA
      name:Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, USA
      name:Department of Neurology, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, USA

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