Literature DB >> 22480202

Structure-based classification and ontology in chemistry.

Janna Hastings1, Despoina Magka, Colin Batchelor, Lian Duan, Robert Stevens, Marcus Ennis, Christoph Steinbeck.   

Abstract

BACKGROUND: Recent years have seen an explosion in the availability of data in the chemistry domain. With this information explosion, however, retrieving relevant results from the available information, and organising those results, become even harder problems. Computational processing is essential to filter and organise the available resources so as to better facilitate the work of scientists. Ontologies encode expert domain knowledge in a hierarchically organised machine-processable format. One such ontology for the chemical domain is ChEBI. ChEBI provides a classification of chemicals based on their structural features and a role or activity-based classification. An example of a structure-based class is 'pentacyclic compound' (compounds containing five-ring structures), while an example of a role-based class is 'analgesic', since many different chemicals can act as analgesics without sharing structural features. Structure-based classification in chemistry exploits elegant regularities and symmetries in the underlying chemical domain. As yet, there has been neither a systematic analysis of the types of structural classification in use in chemistry nor a comparison to the capabilities of available technologies.
RESULTS: We analyze the different categories of structural classes in chemistry, presenting a list of patterns for features found in class definitions. We compare these patterns of class definition to tools which allow for automation of hierarchy construction within cheminformatics and within logic-based ontology technology, going into detail in the latter case with respect to the expressive capabilities of the Web Ontology Language and recent extensions for modelling structured objects. Finally we discuss the relationships and interactions between cheminformatics approaches and logic-based approaches.
CONCLUSION: Systems that perform intelligent reasoning tasks on chemistry data require a diverse set of underlying computational utilities including algorithmic, statistical and logic-based tools. For the task of automatic structure-based classification of chemical entities, essential to managing the vast swathes of chemical data being brought online, systems which are capable of hybrid reasoning combining several different approaches are crucial. We provide a thorough review of the available tools and methodologies, and identify areas of open research.

Entities:  

Year:  2012        PMID: 22480202      PMCID: PMC3361486          DOI: 10.1186/1758-2946-4-8

Source DB:  PubMed          Journal:  J Cheminform        ISSN: 1758-2946            Impact factor:   5.514


  25 in total

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Authors:  Leonid L Chepelev; Janna Hastings; Marcus Ennis; Christoph Steinbeck; Michel Dumontier
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9.  IntAct--open source resource for molecular interaction data.

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Journal:  Nucleic Acids Res       Date:  2006-12-01       Impact factor: 16.971

10.  Chemical Entities of Biological Interest: an update.

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Journal:  Nucleic Acids Res       Date:  2009-10-23       Impact factor: 16.971

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Journal:  J Cheminform       Date:  2012-12-29       Impact factor: 5.514

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8.  libChEBI: an API for accessing the ChEBI database.

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