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Variation ontology: annotator guide

Overview of attention for article published in Journal of Biomedical Semantics, February 2014
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Title
Variation ontology: annotator guide
Published in
Journal of Biomedical Semantics, February 2014
DOI 10.1186/2041-1480-5-9
Pubmed ID
Authors

Mauno Vihinen

Abstract

Systematic representation of information related to genetic and non-genetic variations is required to allow large scale studies, data mining and data integration, and to make it possible to reveal novel relationships between genotype and phenotype. Although lots of variation data is available it is often difficult to use due to lack of systematics.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Netherlands 1 5%
Sweden 1 5%
Mexico 1 5%
Japan 1 5%
United States 1 5%
Unknown 14 74%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 32%
Student > Ph. D. Student 4 21%
Professor 2 11%
Professor > Associate Professor 2 11%
Lecturer 1 5%
Other 2 11%
Unknown 2 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 6 32%
Biochemistry, Genetics and Molecular Biology 4 21%
Computer Science 2 11%
Medicine and Dentistry 2 11%
Mathematics 1 5%
Other 1 5%
Unknown 3 16%