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. 2015 Mar 17;11(3):e1005012. doi: 10.1371/journal.pgen.1005012

Fig 2. Forty non-exclusive patient groups, each group’s patients sharing the same HPO term, amongst whom individual copy number variant candidate genes were each recurrently identified by multiple functional genomics methods and whose recurrently-identified candidate genes demonstrated a significant number of protein-protein interactions.

Fig 2

The dendrogram displays the relationship between categories based upon the number of candidate genes identified by multiple methods that are shared between the phenotype-group patients. Categories are marked if there were significant enrichments using clustering in a gene expression network (Blue), GO (Green) or KEGG (yellow). No phenotype-grouped patients with candidate genes meeting these criteria were identified use mouse KO phenotype (MGI) associations.