If element = NULL
, comparison is plotted based on all elements.
Otherwise, show scatter or GSEA plots for a single element compared with
previously given differential expression results.
referenceComparison
object: obtained after running
rankSimilarPerturbations()
or
predictTargetingDrugs()
Character: identifier in the first column of x
Character: method to plot results; choose between
spearman
, pearson
, gsea
or rankProduct
(the
last one is only available if element = NULL
)
Numeric: number of top and bottom genes to label (if a vector of two
numbers is given, the first and second numbers will be used as the number
of top and bottom genes to label, respectively); only used if
element = NULL
Boolean: show available metadata information instead of
identifiers (if available)? Only used if element = NULL
Boolean: plot non-ranked data in grey? Only
used if element = NULL
Numeric: transparency; only used if element = NULL
Character: when plotting gene set enrichment analysis (GSEA),
plot most up-regulated genes (genes = "top"
), most down-regulated
genes (genes = "bottom"
) or both (genes = "both"
); only used
if method = "gsea"
and geneset = NULL
Extra arguments currently not used
Data frame (GCTX z-scores) or character (respective filepath to load data from file)
Character: plot title (if NULL
, the default title depends
on the context; ignored when plotting multiple perturbations)
Plot illustrating the reference comparison
Other functions related with the ranking of CMap perturbations:
as.table.referenceComparison()
,
filterCMapMetadata()
,
getCMapConditions()
,
getCMapPerturbationTypes()
,
loadCMapData()
,
loadCMapZscores()
,
parseCMapID()
,
plot.perturbationChanges()
,
plotTargetingDrugsVSsimilarPerturbations()
,
prepareCMapPerturbations()
,
print.similarPerturbations()
,
rankSimilarPerturbations()
Other functions related with the prediction of targeting drugs:
as.table.referenceComparison()
,
listExpressionDrugSensitivityAssociation()
,
loadExpressionDrugSensitivityAssociation()
,
plotTargetingDrugsVSsimilarPerturbations()
,
predictTargetingDrugs()
# Example of a differential expression profile
data("diffExprStat")
if (FALSE) { # \dontrun{
# Download and load CMap perturbations to compare with
cellLine <- "HepG2"
cmapMetadataKD <- filterCMapMetadata(
"cmapMetadata.txt", cellLine=cellLine,
perturbationType="Consensus signature from shRNAs targeting the same gene")
cmapPerturbationsKD <- prepareCMapPerturbations(
cmapMetadataKD, "cmapZscores.gctx", "cmapGeneInfo.txt", loadZscores=TRUE)
} # }
# Rank similar CMap perturbations
compareKD <- rankSimilarPerturbations(diffExprStat, cmapPerturbationsKD)
#> Subsetting data based on 8790 intersecting genes (65% of the 13451 input genes)...
#> Comparing against 26 comparisons (1 cell line) using 'spearman, pearson, gsea' (gene size of 150)...
#> Comparison performed in 0.62 secs
# Plot ranked list of CMap perturbations
plot(compareKD, method="spearman")
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
plot(compareKD, method="spearman", n=c(7, 3))
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
plot(compareKD, method="pearson")
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
plot(compareKD, method="gsea")
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
# Plot results for a single perturbation
pert <- compareKD[[1, 1]]
plot(compareKD, pert, method="spearman", zscores=cmapPerturbationsKD)
plot(compareKD, pert, method="pearson", zscores=cmapPerturbationsKD)
plot(compareKD, pert, method="gsea", zscores=cmapPerturbationsKD)
# Predict targeting drugs based on a given differential expression profile
gdsc <- loadExpressionDrugSensitivityAssociation("GDSC 7")
#> Loading data from expressionDrugSensitivityCorGDSC7.qs...
predicted <- predictTargetingDrugs(diffExprStat, gdsc)
#> Subsetting data based on 11396 intersecting genes (85% of the 13451 input genes)...
#> Comparing against 266 GDSC 7 compounds (983 cell lines) using 'spearman, pearson, gsea' (gene size of 150)...
#> Comparison performed in 2.5 secs
# Plot ranked list of targeting drugs
plot(predicted, method="spearman")
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: ggrepel: 229 unlabeled data points (too many overlaps). Consider increasing max.overlaps
plot(predicted, method="spearman", n=c(7, 3))
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: ggrepel: 229 unlabeled data points (too many overlaps). Consider increasing max.overlaps
plot(predicted, method="pearson")
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: ggrepel: 228 unlabeled data points (too many overlaps). Consider increasing max.overlaps
plot(predicted, method="gsea")
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's colour values.
#> Warning: ggrepel: 251 unlabeled data points (too many overlaps). Consider increasing max.overlaps
# Plot results for a single targeting drug
drug <- predicted$compound[[4]]
plot(predicted, drug, method="spearman")
#> Loading data from /tmp/RtmpJcKRtX/file743a73f3f256/reference/expressionDrugSensitivityCorGDSC7.qs...
plot(predicted, drug, method="pearson")
#> Loading data from /tmp/RtmpJcKRtX/file743a73f3f256/reference/expressionDrugSensitivityCorGDSC7.qs...
plot(predicted, drug, method="gsea")
#> Loading data from /tmp/RtmpJcKRtX/file743a73f3f256/reference/expressionDrugSensitivityCorGDSC7.qs...