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This workshop aims to eliminate multiple is_a inheritance in the Cell Ontology 2.0 through relationships to external ontologies like GO and PATO. The goal is to extend the ontology to include additional immune cell types, lay the groundwork for CL 2.0, and fulfill various annotation needs such as flow cytometry results, immune system modeling, and IEDB annotation.
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Cell Ontology 2.0 • Elimination of multiple is_a inheritance through instantiation of relationships to terms in outside ontologies, such as the GO cellular component, GO biological process, and the PATO phenotype ontologies. • Outcome should be more ontologically correct, and more useful for data analysis. • Process is likely to be slow, due to lack of personnel and funding to organize the work.
Goals for this Workshop(per Alex) Pragmatic Goal Extend the ontology in its current form to include additional immune cell types. Ideal Outcome Lay the groundwork for CL 2.0 in the area of immune cell types.
Use Cases for Cell Ontology Annotation (ongoing for GO). Cross product term formation with GO, MP, and other ontologies (ongoing). Representation of Flow Cytometry Results. Immune System Modeling. IEDB annotation needs. Other?
How do we describe Cells? • Morphology • Surface markers • Transcription factors • Location • Role or process involvement • Lineage
How do we describe Cells? Link to external ontology • Morphology • Surface markers • Transcription factors • Location • Role or process involvement • Lineage Protein Ontology Anatomy Ontology GO Biological Process
How do we describe Cells? Link via specific relationships • Morphology • Surface markers • Transcription factors • Location • Role or process involvement • Lineage expresses_protein located_in participates_in
Issues to Discuss Distinction between ontology, knowledgebase, and vocabulary. How much information is needed to describe a cell uniquely — to create a formal definition? How to deal with species differences.