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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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Publications

  • (Smedley et al., 2013) PhenoDigm: analyzing curated annotations to associate animal models with human diseases. Database.
    PMID: 23660285

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