| Literature DB >> 20509878 |
Abstract
BACKGROUND: With the continuously increasing demands on knowledge- and data-management that databases have to meet, ontologies and the theories of granularity they use become more and more important. Unfortunately, currently used theories and schemes of granularity unnecessarily limit the performance of ontologies due to two shortcomings: (i) they do not allow the integration of multiple granularity perspectives into one granularity framework; (ii) they are not applicable to cumulative-constitutively organized material entities, which cover most of the biomedical material entities.Entities:
Mesh:
Year: 2010 PMID: 20509878 PMCID: PMC3098069 DOI: 10.1186/1471-2105-11-289
Source DB: PubMed Journal: BMC Bioinformatics ISSN: 1471-2105 Impact factor: 3.169
Figure 1Four different Types of Hierarchies used in Biology. A) A constitutive hierarchy of molecules, organelles, cells, and organs of a multicellular organism, in which all molecules are contained in organelles, all organelles in cells, and all cells in organs. B) The more realistic case of a cumulative constitutive hierarchy of molecules, organelles, cells and organs of a multicellular organism, in which not all molecules are contained in organelles or cells, and not all cells in organs. C) An aggregative hierarchy of species being aggregated to genera, genera to families and families to orders, just like in a traditional Linnaean taxonomy. D) A cumulative aggregative hierarchy, as it can be found in the hierarchical organization of military stuff, in which individuals with higher ranks (i.e. sergeants, lieutenants, captains) 'emerge' in aggregates of higher order (i.e. squads, platoons, companies).
Figure 2Granularity of Instance vs Granularity of Types. A) Compositional object partitions of an organ. Three partitions are shown: (i) into cells (q, r) and extracellular molecules (a-d); (ii) into organelles (m-p) and cellular molecules (a-h); and (iii) into organelle molecules (a-l). B) The bona fide granularity tree based on these three partitions. The organ itself and each of its partitions represent a cut in the tree and thus an instance granularity level. C) The extension of 'molecule' (i.e. the distribution of instances of 'molecule') of the organ crosses the boundaries of instance granularity levels. Therefore, the instance granularity tree cannot be directly transformed into or mapped upon a type granularity tree. But by following the simple and intuitive rule that a type occupies the lowest granularity level of its instances, one can nevertheless infer granularity levels for types.
Granularity Schemes used in Ontologies of Anatomy.
| Levels of Granularity [ordered from fine < coarse] | Domain/Application | Parent Class Affiliation | Ontology/Controlled Vocabulary | Version |
|---|---|---|---|---|
| 'macromolecular complex' < 'organelle part' < 'organelle' < 'cell part' < 'cell'; | genomic and proteomic | 'cellular component' | 1.689 | |
| human anatomy - to a limited degree also vertebrate anatomy | 'Anatomical structure' | 3.0 | ||
| medical coding and classification, medical terminologies, | 'MicroscopicStructure'; 'OrganicSolidStructure' | 1.1 | ||
| 'Microanatomic Structure' [i.e.: 'Macromolecular Structure' < 'Cell'] < 'Tissue' < 'Organ' < 'Organ System' < 'Body Part' - 'Body Region'; | medical coding for clinical care, translational and basic research, and public information and administrative activities | 'Anatomical Structure, System, or Substance' | 09.07 | |
| clinical terms | 'Anatomical structure' | 2009_01_31 | ||
| 'cell' < 'portion of tissue' < 'multi-tissue structure' < 'compound organ' < 'organism subdivision' < 'whole organism' | Zebrafish anatomy and development | 'anatomical structure' | 1.22 | |
| Xenopus anatomy and development | 1.19 | |||
| 'cell' < 'portion of tissue' < 'multi-tissue structure' < 'compound organ' < 'organism subdivision' < 'body' | multispecies fish anatomy | 'anatomical structure' | 1.120 | |
| 'Biological small molecule' < 'Biological Macromolecule' < 'Cell part' < 'Cell' < 'gross anat structure' < 'Organism'; | vertebrate anatomy; derived mainly from FMA | 'Biological object'' | 1.1 | |
| anatomical dictionary for the adult mouse | 'adult mouse' | 1.195 | ||
| standard terms for annotating mammalian phenotypic data | 'mammalian phenotype' | 1.298 | ||
| a structured controlled vocabulary of the anatomy of Amphibians | - | 1.8 | ||
| 'Anatomy', 'Cell', 'Nucleus'; | anatomy of | 'C. elegans Cell and Anatomy Ontology' | 1.31 | |
| 'cell component' < 'multi-cell-component structure' < 'cell' < 'portion of tissue' < 'multi-tissue structure' < 'organ system subdivision' < 'organ system' < 'organism subdivision' < 'organism'; | anatomy of | 'anatomical structure' | 1.30 | |
| 'cell component' < 'cells' < 'portion of tissue' < 'multi-tissue structure' < 'compound organ' < 'organism subdivision' < 'multi-cellular organism' | a structured controlled vocabulary of the anatomy of mosquitoes. | 'anatomical structure' | 1.10 | |
| 'acellular anatomical structure', 'portion of organism substance', 'whole organism'; | an ontology for spider comparative biology including anatomical parts, behavior, and products | 'anatomical entity' | 1.17 | |
| 'cell component' < 'cell' < 'portion of tissue' < 'multi-tissue structure' < 'compound organ' < 'organism subdivision' < 'multi-cellular organism' | anatomy of Hymenoptera | 'anatomical structure' | SVN Revision 2804 | |
| 'cell component' < 'cell' < 'portion of tissue' < 'multi-tissue structure' < 'compound organ' < 'organism subdivision' < 'multi-cellular organism' | anatomy of Bilateria | 'anatomical structure' | - | |
| 'plant cell' < 'tissue' < 'organ' < 'whole plant' | botanical anatomy & morphology | 'plant structure' | 1.64 | |
| a structured controlled vocabulary for the anatomy of fungi. | 'microbial structure ontology' | 1.3 | ||
| biomedical structures from macromolecules to supracellular level | 'fiat object part', 'object', 'object aggregate' | 1.2.5 | ||
| 'cell component' < 'cell' < 'portion of tissue' < 'multi-tissue structure' < 'compound organ' < 'organism subdivision' < 'multi-cellular organism' | cross-species anatomy: platform for integrating different species-specific anatomy ontologies | 'anatomical structure' | 1.3 | |
| multi-species anatomy, generated from union of existing species-specific anatomy ontologies | 'anatomical structure' | 1.72 | ||
| Minimal set of terms for anatomy | 'animal component' | 1.1 | ||
| 'subatomic particle' < 'atom' < 'molecular entity' < 'poly molecular composite Entity' [i.e. 'molecular complex' < 'structured nonbiological entity'/'structured biological entity' [i.e. 'cellular component' < 'cell' < 'organism part' < 'organism']] | biomedicine | 'material entity' | - | |
Various ontologies and their partly implicit, partly explicit levels of granularity of anatomical structures (from [50]).
Definitions of the Basic Formal Ontology.
| Definition | Parent Class Affiliation | Link/ID |
|---|---|---|
| 'independent continuant' | ||
| 'material entity' | ||
| 'material entity' | ||
| 'material entity' | ||
Definitions of the top-level types of material entity of the Basic Formal Ontology (BFO version 1.1).
Figure 3Examples of Compositional and Spatial Partitions. A) A combination of compositional partitions of an object into objects of a lower level of granularity as its constitutional parts. Exemplified by three partitions of an organ: A partition into cells, one into organelles, and one into molecules. B) A spatial partition of an object into fiat object parts as its regional parts. Exemplified by the partition of an organ into three fiat organ parts. C) A spatial partition of an object into fiat object parts as its regional parts. Exemplified by the partition of an organ into two cell aggregates with ECM. D) A spatial partition of an object into fiat object parts as its regional parts. Exemplified by the partition of an organ into a cell part aggregate with ECM and a cell aggregate with ECM. ECM: extracellular matrix.
Figure 4Scale dependent Resolution. A) On the molecular level, individual molecules and aggregates thereof can be distinguished and are referred to by using count-nouns (i.e. 'molecule'; 'molecule aggregate'). B) On the organelle level, individual organelles can be distinguished and are referred to by using count-nouns (i.e. 'organelle'). Individual molecules and aggregates thereof, however, are usually not distinguished anymore and one refers to them by using mass-nouns, such as 'portion of molecular substance'. One can distinguish extra-organelle from intra-organelle portions of molecular substance. C) On the cellular level, individual cells can be distinguished and are referred to by the count-nouns 'cell' or 'cell cluster with ECM' (or its resolution-dependent countable representation 'cell cluster with portion of ECM'). Individual organelles, however, are usually not distinguished anymore. Instead, one refers to the extracellular matter as non-countable 'portion of ECM', whereas the intracellular matter represents a granular mixture of non-countable organelles and cytoplasm and is referred to as 'portion of organelles and cytoplasm'. Both represent mass-nouns. D) On the organ level, individual cells are usually not distinguished anymore. Instead, one refers to the matter contained in organs as a 'portion of tissue', which is the resolution-dependent non-countable representation of 'cell aggregate with ECM'. 'Portion of tissue' therewith represents a mass-noun. ECM: extracellular matrix.
Figure 5Compositional Object Granularity Perspective. A particular qualitative compositional object granularity perspective that is defined in reference to a combination of direct proper parthood and the defining properties of 'object' as its granulation criterion. The levels of granularity are demarcated according to the defining properties of different subtypes of 'object' that possess proper parthood relations to other such subtypes (e.g. 'Organelle', 'Cell', 'Organ'), and they are ordered according to the direction of direct-proper-part-of relations.
Figure 6Additional Compositional Granularity Perspectives. A combination of three particular qualitative compositional object of fiat object part granularity perspectives. Each perspective is defined in reference to a combination of direct proper parthood and either the defining properties of specific subtypes of 'object' (in the perspectives depicted it is 'cell'), all of which belong to the same compositional object granularity level, or the defining properties of their respective type of 'fiat object part', of which the object entities are direct proper part of (in the perspectives depicted these are 'cell aggregate with ECM', 'fiat organ part', and 'fiat organ part aggregate'). Each of these additional compositional granularity perspectives contains only two levels: a lower level, to which subtypes of 'object' belong (e.g. 'cell'), and a higher level, to which subtypes of 'fiat object part' belong (e.g., 'cell aggregate with ECM', 'fiat organ part', or 'fiat organ part aggregate'). Notice that the three perspectives shown overlap with one another at their 'cell' levels - a particular cell can belong to all three perspectives at the same time. ECM: extracellular matrix.
Figure 7The General Integrated Spatio-Structural Granularity Framework. Some of its granularity perspectives are shown and how they relate, i.e. overcross, with one another.
Figure 8Overview of the Framework. Overview of the different types of compositional, spatial, and resolution granularity perspectives of the General Integrated Spatio-Structural Granularity Framework and how they relate to the basic subtypes of 'material entity', with 'Cell', 'Organ', 'Cell aggregate with ECM', 'Cell part aggregate with ECM', 'Organ part aggregate with portion of tissue', and 'Fiat organ part' as examples. The arrows indicate whether it is a compositional, a spatial, or a resolution perspective and how many granularity levels it distinguishes. Different subtypes of 'fiat object part' are distinguished (i.e. 'Cell part aggregate with ECM', 'Organ part aggregate with portion of tissue', 'Cell aggregate with ECM', and 'Fiat organ part'), which allow the differentiation of further subtypes of spatial and compositional granularity perspectives, which, however, are not discussed in detail here. All perspectives involving object aggregates are not covered in detail, since they are of limited relevance for cumulative-constitutively organized entities. ECM: extracellular matrix.
Figure 9Basic Spatial Granularity Perspectives. A combination of three particular qualitative spatial fiat object part of object granularity perspectives. Each perspective is defined in reference to a combination of proper parthood and either the defining properties of specific subtypes of 'object' (in the perspectives depicted it is 'organ'), all of which belong to the same compositional object granularity level, or the defining properties of their respective 'fiat object part' parts (in the perspectives depicted these are 'cell aggregate with ECM', 'fiat organ part', and 'cell part aggregate with ECM'). Each basic spatial granularity perspective contains only two levels: a lower level, to which subtypes of 'fiat object part' belong (e.g., 'cell aggregate with ECM', 'fiat organ part', or 'cell part aggregate with ECM'), and a higher level, to which subtypes of 'object' belong (e.g., 'organ'). Notice that the three perspectives shown overlap with one another at their 'organ' levels - a particular organ can belong to all three perspectives at the same time. ECM: extracellular matrix.
Figure 10Resolution Granularity Perspective. A particular quantitative scale dependent resolution of object aggregate with fiat object part granularity perspective. Each resolution perspective is defined in reference to a combination of a proper countable parthood relation with a is-representation-of relation and the defining properties of all subtypes of 'object aggregate' or 'object aggregate with fiat object part' that belong to the same compositional object aggregate of object granularity perspective or the same spatial fiat object part of object granularity perspective respectively (depicted is the resolution perspective of cell aggregate with ECM, a particular resolution of object aggregate with fiat object part granularity perspective). Each resolution granularity perspective contains only two levels: a lower level, to which subtypes of 'object cluster' or 'object cluster with portion of substance' (e.g., 'cell cluster with portion of ECM') belong that represent countable representations of the corresponding subtypes of 'object aggregate' or 'object aggregate with fiat object part' (e.g., 'cell aggregate with ECM') respectively, and a higher level, to which subtypes of 'portion of substance' or 'portion of granular mixture of substance X and Y' (e.g., 'portion of tissue') belong that represent the non-countable representations of the same object aggregate or object aggregate with fiat object part. ECM: extracellular matrix.
Figure 11Example of how Structural Granularity Values are assigned to a given Partition. Example for a particular granular partition of an organ into its fiat organ part and cell parts. Shown is a chain of proper parthood relations, starting from a particular cell, that is part of a specific fiat organ part 1, which at its turn is part of a fiat organ part 2 that is part of a fiat organ part 3, which is part of an organ. The structural granularity values of the respective object entities (i.e. cell and organ) can be inferred using the fix natural number values from the compositional object granularity perspective: value X for the cell entity and value (X+1) for the organ entity. The structural granularity values of the different fiat organ part entities must be within the range of X and (X+1), as the overcrossing spatial granularity perspectives imply. With the finer-grained relation ' < ', the respective value interval 'X to (X+1)' can be further confined for each particular fiat organ part entity in the way it is shown in this figure.