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4 changes: 2 additions & 2 deletions DESCRIPTION
Original file line number Diff line number Diff line change
@@ -1,7 +1,7 @@
Package: Moonlight2R
Type: Package
Title: Identify oncogenes and tumor suppressor genes from omics data
Version: 1.11.0
Version: 1.11.1
Date:
Authors@R:
c(person("Mona", "Nourbakhsh",
Expand Down Expand Up @@ -90,7 +90,7 @@ SystemRequirements: CScapeSomatic
VignetteBuilder: knitr
URL: https://github.com/ELELAB/Moonlight2R
BugReports: https://github.com/ELELAB/Moonlight2R/issues
RoxygenNote: 7.3.3
LazyData: false
Encoding: UTF-8
Config/testthat/edition: 3
Config/roxygen2/version: 8.0.0
6 changes: 6 additions & 0 deletions NEWS.md
Original file line number Diff line number Diff line change
@@ -1,3 +1,9 @@
# Moonlight2R 1.11.1

## Summary

* Fix FEA Moonlight Z-score to consider experimental logFC in the score calculation

# Moonlight2R 1.9.4

## Summary
Expand Down
69 changes: 32 additions & 37 deletions R/FEA.R
Original file line number Diff line number Diff line change
Expand Up @@ -25,7 +25,7 @@ FEA <- function(BPname = NULL,

# List of variable names
variables_to_check <- c("DiseaseList", "EAGenes")

# Check and load variables if they do not exist
for (variable_name in variables_to_check) {
if (! variable_name %in% names(.GlobalEnv)) {
Expand Down Expand Up @@ -74,7 +74,6 @@ FEA <- function(BPname = NULL,
# sorting strategy to avoid different sorting in case of tie ranks
rankings <- rankings[order(-rankings, names(rankings))]


pathwayNamesList <- list()
for (k in seq_along(lf2)) {

Expand All @@ -101,11 +100,24 @@ FEA <- function(BPname = NULL,
res <- as.data.frame(matrix(0, nrow = 1, ncol = 2,
dimnames = list(1, c("pathway",
"Moonlight.Z.score"))))



pathway_data <- fgseaRes[fgseaRes$pathway == lf2[k],]

leadingEdge_genes <- unlist(pathway_data$leadingEdge)

selected_diseases <- as.data.frame(DiseaseList[[which(names(DiseaseList) == lf2[k])]])

selected_diseases <- selected_diseases[selected_diseases$ID %in% leadingEdge_genes, ]

res$pathway <- lf2[k]

selected_diseases$logFC <- DiffMatrix$logFC[match(selected_diseases$ID, rownames(DiffMatrix))]

selected_diseases <- selected_diseases[!is.na(selected_diseases$logFC), ]


Zscore <- .compute_moonlight_zscore(selected_diseases)

res$Moonlight.Z.score <- Zscore
Expand All @@ -124,7 +136,7 @@ FEA <- function(BPname = NULL,
rename("Diseases.or.Functions.Annotation" = pathway, "p.value" = pval) %>%
select("Diseases.or.Functions.Annotation", "Moonlight.Z.score","p.value", "padj", "ES", "NES", "size", "leadingEdge")


}
else if (method == "ora") {

Expand Down Expand Up @@ -173,37 +185,17 @@ FEA <- function(BPname = NULL,
}

GeneList <- GeneList[GeneList$PROBE_ID %in% selected_diseases$ID, ]

selected_diseases <- selected_diseases[selected_diseases$ID %in% GeneList[, "PROBE_ID"], ]
selected_diseases[, "Exp.Log.Ratio"] <- gsub(",", ".", selected_diseases[, "Exp.Log.Ratio"])
selected_diseases[, "Exp.Log.Ratio"] <- as.numeric(selected_diseases[, "Exp.Log.Ratio"])

rownames(selected_diseases) <- selected_diseases$ID
selected_diseases$logFC <- GeneList$logFC[match(selected_diseases$ID, GeneList$PROBE_ID)]

selected_diseases <- selected_diseases[!is.na(selected_diseases$logFC), ]

rownames(selected_diseases) <- selected_diseases$ID

res$Molecules <- paste0(GeneList$PROBE_ID, collapse = ",")

for (idx in seq.int(nrow(selected_diseases))) {

currTR <- selected_diseases$ID[idx]

if (length(grep("Increases", selected_diseases[currTR, "Findings"])) == 1) {

if (sign(GeneList[currTR, "logFC"]) > 0) {
selected_diseases[currTR, "Prediction..based.on.expression.direction."] <- "Increased"
} else if (sign(GeneList[currTR, "logFC"]) < 0) {
selected_diseases[currTR, "Prediction..based.on.expression.direction."] <- "Decreased"
}
}

if (length(grep("Decreases", selected_diseases[currTR, "Findings"])) == 1) {
if (sign(GeneList[currTR, "logFC"]) < 0) {
selected_diseases[currTR, "Prediction..based.on.expression.direction."] <- "Increased"
} else if (sign(GeneList[currTR, "logFC"]) > 0) {
selected_diseases[currTR, "Prediction..based.on.expression.direction."] <- "Decreased"
}
}
}

Zscore <- .compute_moonlight_zscore(selected_diseases)

res$Moonlight.Z.score <- Zscore
Expand Down Expand Up @@ -237,22 +229,25 @@ FEA <- function(BPname = NULL,
#' @noRd
.compute_moonlight_zscore <- function(selected_diseases) {

if(!all(c("Findings", "logFC") %in% colnames(selected_diseases))){
stop("The input DiseaseList does not contain 'Findings' and 'logFC' columns for Moonlight z-score calculations")
}

Correlation <- matrix(0, nrow(selected_diseases), 1)

selected_diseases <- cbind(selected_diseases, Correlation)

if (length(grep("Decreases", selected_diseases$Findings)) != 0) {
if (any(grepl("Increases|Decreases", selected_diseases$Findings, ignore.case = TRUE))){

selected_diseases[grep("Decreases", selected_diseases$Findings), "Findings"] <- -1
selected_diseases[grep("Increases", selected_diseases$Findings), "Findings"] <- 1
selected_diseases[grep("Affects", selected_diseases$Findings), "Findings"] <- 0
selected_diseases[, "Findings"] <- as.numeric(selected_diseases[, "Findings"])

selected_diseases[, "Exp.Log.Ratio"] <- gsub(",", ".", selected_diseases[, "Exp.Log.Ratio"])
selected_diseases[, "Exp.Log.Ratio"] <- as.numeric(selected_diseases[, "Exp.Log.Ratio"])
PredictionIncreased <- which(sign(selected_diseases$Exp.Log.Ratio) == selected_diseases$Findings)
PredictionDecreased <- which(sign(selected_diseases$Exp.Log.Ratio) != selected_diseases$Findings)
selected_diseases[, "logFC"] <- gsub(",", ".", selected_diseases[, "logFC"])
selected_diseases[, "logFC"] <- as.numeric(selected_diseases[, "logFC"])

PredictionIncreased <- which(sign(selected_diseases$logFC) == selected_diseases$Findings)
PredictionDecreased <- which(sign(selected_diseases$logFC) != selected_diseases$Findings)
PredictionAffected <- which(sign(selected_diseases$Findings) == 0)

selected_diseases[PredictionIncreased, "Correlation"] <- 1
Expand All @@ -263,7 +258,7 @@ FEA <- function(BPname = NULL,
} else {
Zscore <- 0
}

return(Zscore)

}
2 changes: 1 addition & 1 deletion R/PRA.R
Original file line number Diff line number Diff line change
Expand Up @@ -13,7 +13,7 @@
#' data(DiseaseList)
#' data(tabGrowBlock)
#' data(knownDriverGenes)
#' dataPRA <- PRA(dataURA = dataURA[seq.int(2),],
#' dataPRA <- PRA(dataURA = dataURA,
#' BPname = c("apoptosis","proliferation of cells"),
#' thres.role = 0)
PRA <- function(dataURA,
Expand Down
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2 changes: 1 addition & 1 deletion man/PRA.Rd

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16 changes: 8 additions & 8 deletions tests/testthat/test-TFinfluence.R
Original file line number Diff line number Diff line change
Expand Up @@ -9,17 +9,17 @@ data(dataMAVISp)


reference_TFresults <- data.frame(
Target = c("CHST1", "GEN1", "TAP1", "TAP1"),
Moonlight_gene_z_score = c(1.06066017177982, 1.30096115353815, 0.8262079533974, 0.8262079533974),
Moonlight_Oncogenic_Mediator = c("TSG", "OCG", "OCG", "OCG"),
logFC_target = c(1.94917640749552, 1.36435629696216, 1.36486453774995, 1.36486453774995),
TF = c(NA, NA, "IRF1", "IRF2"),
InteractionType = c(NA, NA, "Activation", "Activation"),
PMID = c(NA, NA, "18694960", "15778351"),
Target = c("PDE2A", "GCAT", "ARMC9", "FAM155A"),
Moonlight_gene_z_score = c(1.37642904406401, 0.810977174901446, 0.367466020609254, 1.19863281130568),
Moonlight_Oncogenic_Mediator = c("TSG", "TSG", "TSG", "OCG"),
logFC_target = c(-3.36278468754307, 1.0407914607103, 1.03363210942098, 1.97338960700756),
TF = as.character(c(NA, NA, NA, NA)),
InteractionType = as.character(c(NA, NA, NA, NA)),
PMID = as.character(c(NA, NA, NA, NA)),
tf_mutation = as.character(c(NA, NA, NA, NA)),
stab_class = as.character(c(NA, NA, NA, NA)),
in_MAVISp = c(FALSE,FALSE,FALSE,FALSE),
mutation_available = c(FALSE,FALSE,FALSE,FALSE),
mutation_available = c(FALSE, FALSE, FALSE, FALSE),
stringsAsFactors = FALSE
)

Expand Down
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