Abstract

Researchers use animal studies to better understand human diseases. In recent years, large-scale phenotype studies such as Phenoscape and EuroPhenome have been initiated to identify genetic causes of a species' phenome. Species-specific phenotype ontologies are required to capture and report about all findings and to automatically infer results relevant to human diseases. The integration of the different phenotype ontologies into a coherent framework is necessary to achieve interoperability for cross-species research.Here, we investigate the quality and completeness of two different methods to align the Human Phenotype Ontology and the Mammalian Phenotype Ontology. The first method combines lexical matching with inference over the ontologies' taxonomic structures, while the second method uses a mapping algorithm based on the formal definitions of the ontologies. Neither method could map all concepts. Despite the formal definitions method provides mappings for more concepts than does the lexical matching method, it does not outperform the lexical matching in a biological use case. Our results suggest that combining both approaches will yield a better mappings in terms of completeness, specificity and application purposes.

Highlights

  • Large-scale mutagenesis projects aim to identify the phenotypes of organisms resulting from modifications to the organisms’ genetic markup and thereby provide the tantalizing possibility for revealing valuable information about the molecular mechanisms underlying human disease [1]

  • The lower number of mapped concepts for one particular concept suggests that the formal definitions method maps to more generalized concepts of the other ontology

  • The number of mapped concepts and the specificity of the mappings generated by the formal definitions method depends solely on the availability and quality of the formal definitions for both ontologies, which constitutes an advantage at the same time

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Summary

Introduction

Large-scale mutagenesis projects aim to identify the phenotypes of organisms resulting from modifications to the organisms’ genetic markup and thereby provide the tantalizing possibility for revealing valuable information about the molecular mechanisms underlying human disease [1]. Lexical mappings between the labels of concepts in species-specific phenotype ontologies are used to identify related phenotypes in different species. One implementation of this approach is the Lexical OWL Ontology Matcher (LOOM) [7] which has been shown to perform well on aligning anatomical ontologies. The second approach is implemented in the PhenomeBLAST software [11] and both, software and the resulting mappings, are publicly available from http://phenomeblast.googlecode.com

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