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Try 'pruning' the terms associated with 'Pancreatic Stellate Cells'... if all leaf nodes of a parent are enriched, then drop the leaf terms. Then we can see a cleaner list of what phenotypes are associated with it about rare_disease_celltyping HOT 1 CLOSED

NathanSkene avatar NathanSkene commented on June 14, 2024
Try 'pruning' the terms associated with 'Pancreatic Stellate Cells'... if all leaf nodes of a parent are enriched, then drop the leaf terms. Then we can see a cleaner list of what phenotypes are associated with it

from rare_disease_celltyping.

Comments (1)

bschilder avatar bschilder commented on June 14, 2024

Took a somewhat inverted approach by checking if each term have an descendants. If it does, only include its most precise descendants. This helps remove redundant terms in the target prioritisation pipeline, while retaining maximum precision of phenoptypes.

library(KGExplorer)
dat <- data.table::data.table(hpo_id=c("HP:0000001","HP:0000002","HP:0000003"),
                             name=c("term1","term2","term3"))
ont <- get_ontology("hp")
dat2 <- prune_ancestors(dat,ont=ont)

from rare_disease_celltyping.

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