Motivation: Phenotypic information is important for the analysis of the molecular mechanisms underlying disease. A formal ontological representation of phenotypic information can help to identify, interpret and infer phenotypic traits based on experimental findings. The methods that are currently used to represent data and information about phenotypes fail to make the semantics of the phenotypic trait explicit and do not interoperate with ontologies of anatomy and other domains. Therefore, valuable resources for the analysis of phenotype studies remain unconnected and inaccessible to automated analysis and reasoning.Results: We provide a framework to formalize phenotypic descriptions and make their semantics explicit. Based on this formaliz...
Scientists and clinicians who study genetic alterations and disease have traditionally described phe...
Neurodegenerative diseases present a wide and complex range of biological and clinical features. An...
The past decade has seen an explosion in the collection of genotype data in domains as diverse as me...
Motivation: Phenotypic information is important for the analysis of the molecular mechanisms underly...
The past decade has seen an explosion in the collection of genotype data in domains as diverse as me...
BACKGROUND: Integration and analysis of phenotype data from humans and model organisms is a key chal...
Phenotypes are investigated in model organisms to understand and reveal the molecular mechanisms und...
Abstract Background Integration and analysis of phenotype data from humans and model organisms is a ...
Motivation: The systematic observation of phenotypes has become a crucial tool of functional genomic...
Contains fulltext : 136954.pdf (publisher's version ) (Open Access)The Human Pheno...
The systematic investigation of the phenotypes associated with genotypes in model organisms holds th...
The path to disease gene discovery in humans is often a lengthy one, but can be significantly shorte...
The Human Phenotype Ontology (HPO) consists of a well-defined and comprehensive set of more than 12,...
The systematic investigation of the phenotypes associated with genotypes in model organisms holds th...
The Human Phenotype Ontology (HPO) project, available at http://www.human-phenotype-ontology.org, pr...
Scientists and clinicians who study genetic alterations and disease have traditionally described phe...
Neurodegenerative diseases present a wide and complex range of biological and clinical features. An...
The past decade has seen an explosion in the collection of genotype data in domains as diverse as me...
Motivation: Phenotypic information is important for the analysis of the molecular mechanisms underly...
The past decade has seen an explosion in the collection of genotype data in domains as diverse as me...
BACKGROUND: Integration and analysis of phenotype data from humans and model organisms is a key chal...
Phenotypes are investigated in model organisms to understand and reveal the molecular mechanisms und...
Abstract Background Integration and analysis of phenotype data from humans and model organisms is a ...
Motivation: The systematic observation of phenotypes has become a crucial tool of functional genomic...
Contains fulltext : 136954.pdf (publisher's version ) (Open Access)The Human Pheno...
The systematic investigation of the phenotypes associated with genotypes in model organisms holds th...
The path to disease gene discovery in humans is often a lengthy one, but can be significantly shorte...
The Human Phenotype Ontology (HPO) consists of a well-defined and comprehensive set of more than 12,...
The systematic investigation of the phenotypes associated with genotypes in model organisms holds th...
The Human Phenotype Ontology (HPO) project, available at http://www.human-phenotype-ontology.org, pr...
Scientists and clinicians who study genetic alterations and disease have traditionally described phe...
Neurodegenerative diseases present a wide and complex range of biological and clinical features. An...
The past decade has seen an explosion in the collection of genotype data in domains as diverse as me...