hpDef {PCAN}R Documentation

Description of HP terms (Example data)

Description

HP terms basic information. Only descendants of 'Phenotypic abnormality' were taken into account.

Format

A data frame with 10962 rows and 2 columns:

id

HP term IDs

name

HP term names

Details

These data are used to examplify the different functions of the package. More data are available in the MultiHumanPhenoDB package.

Source

http://compbio.charite.de/hudson/job/hpo/1529/artifact/hp/hp.obo

Examples

## Prerequisite
data(geneByHp, hp_descendants, package="PCAN")
geneByHp <- unstack(geneByHp, entrez~hp)
ic <- computeHpIC(geneByHp, hp_descendants)

## Compute similarity between different couples of HP terms
data(hp_ancestors, hpDef, package="PCAN")
hp1 <- "HP:0000518"
hp2 <- "HP:0030084"
hp3 <- "HP:0002119"
hp4 <- "HP:0001305"
hpDef[which(hpDef$id %in% c(hp1, hp2)), 1:2]
calcHpSim(hp1, hp2, IC=ic, ancestors=hp_ancestors)
hpDef[which(hpDef$id %in% c(hp2, hp3)), 1:2]
calcHpSim(hp2, hp3, IC=ic, ancestors=hp_ancestors)
hpDef[which(hpDef$id %in% c(hp2, hp4)), 1:2]
calcHpSim(hp2, hp4, IC=ic, ancestors=hp_ancestors)
hpDef[which(hpDef$id %in% c(hp3, hp4)), 1:2]
calcHpSim(hp3, hp4, IC=ic, ancestors=hp_ancestors)

[Package PCAN version 1.20.0 Index]