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PHENOtype comparisons for DIsease and Gene Models PhenoDigm

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An automated method to provide evidence about gene-disease associations by analysing phenotype information. PhenoDigm integrates data from a variety of model organisms and, at the same time, uses several intermediate scoring methods to identify only strongly data-supported gene candidates for human genetic diseases.

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PhenoDigm classification

PhenoDigm specifications

Restrictions to use:
None
Maintained:
Yes

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Publications

Institution(s)

Mouse Informatics Group, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB, UK

Link to literature

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