Comments (1)
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.
Related Issues (20)
- Describe Human Cell Landscape CTD levels HOT 2
- Assess pLI in HPO genes HOT 6
- `phenomix`: Exploring more efficient methods for celltype enrichment HOT 5
- Identify variant-level mechanisms of each rare disease HOT 3
- Update website with the results from the new scRNA-seq datasets HOT 1
- Assess our results against known phenotype-celltype links HOT 4
- Regenerate manuscript figures with new results HOT 2
- Rewrite manuscript HOT 2
- Remake equations with color coding HOT 1
- Adjust congenital onset figure HOT 1
- Remove diagnosis/prognosis figures
- Redo Monarch recall stats HOT 1
- Create static versions of network plots
- Adjust ontology levels figure HOT 5
- Rework target prioritisation figure HOT 1
- Assess distribution of congenital phenotypes HOT 7
- Target prioritisation pipeline figure HOT 5
- Move AD/PD networks to supplementary materials HOT 1
- Include animal model availability in target prioritisation pipeline HOT 1
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from rare_disease_celltyping.