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Fig. 2 | BMC Bioinformatics

Fig. 2

From: PCAN: phenotype consensus analysis to support disease-gene association

Fig. 2

PCAN prior knowledge resources. Public resources used to link genes to phenotypic abnormalities based on the genetic diseases each gene causes. The HPO phenotype annotation resource (build #1039) was used to link HP terms to OMIM disorders and ClinVar (version of May 2015) was used to retrieve genes that cause OMIM disorders. Total counts of each distinct entity type in the resultant gene-trait resource are provided

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