#Loading packages
#Setting default width option
apiUrl <- "http://www.ilincs.org/api/SignatureLibraries"
req <- GET(apiUrl)
json <- httr::content(req, as = "text")
ilincs_libraries <- fromJSON(json)
ilincs_libraries[,c("libraryID","libraryName")]
term <- "MTOR"
ilincs_libId<-"LIB_6"
apiUrl <- paste("http://www.ilincs.org/api/SignatureMeta/findTermWithSynonyms?term=",term,"&library=",ilincs_libId,sep="")
req <- GET(apiUrl)
mtorCgs<-fromJSON(httr::content(req,type="text"))$data
## No encoding supplied: defaulting to UTF-8.
mtorCgsMcf7<-mtorCgs[intersect(grep("MCF7",mtorCgs$cellline),grep("trt_xpr.cgs",mtorCgs$pert_type)),]
mtorCgsMcf7[,c("cellline","time","treatment","signatureid","pert_type")]
ilincs_signatureId <- mtorCgsMcf7$signatureid[1]
apiUrl <- paste("http://www.ilincs.org/api/SignatureMeta/findConcordantSignatures?sigID=",ilincs_signatureId,"&lib=",ilincs_libId,sep="")
req <- GET(apiUrl)
connectedCgs<-fromJSON(httr::content(req,type="text"))
## No encoding supplied: defaulting to UTF-8.
head(connectedCgs[,c("signatureid","similarity","pValue","cellline","treatment")])
geneFreq <- sort(table(connectedCgs$treatment[1:100]),decreasing=TRUE)[5:1]
geneFreqDf<-data.frame(gene=factor(names(geneFreq),levels=names(geneFreq),ordered=T),geneFreq=as.vector(geneFreq))
tp100cgs<-ggplot(data=geneFreqDf,aes(x=gene,y=geneFreq)) +
geom_bar(stat="identity",fill="steelblue") +
coord_flip() + theme_bw() +
theme(axis.ticks=element_line(color="grey80"),text=element_text(size=20),legend.key.size=unit(1,"cm"),axis.line.x=element_line(colour="black"),panel.grid.major=element_blank(),panel.grid.minor=element_blank(),panel.border=element_blank(),panel.background=element_blank()) +
labs(x="",y="Number of Signatures")
print(tp100cgs)
ilincs_libId<-"LIB_5"
apiUrl <- paste("http://www.ilincs.org/api/SignatureMeta/findConcordantSignatures?sigID=",ilincs_signatureId,"&lib=",ilincs_libId,sep="")
req <- GET(apiUrl)
connectedCps<-fromJSON(httr::content(req,type="text"))
## No encoding supplied: defaulting to UTF-8.
head(connectedCps)
top100GeneTargets<-unlist(strsplit(connectedCps$GeneTargets[1:100],split="\\|"))
geneFreq <- sort(table(top100GeneTargets),decreasing=TRUE)[5:1]
geneFreqDf<-data.frame(gene=factor(names(geneFreq),levels=names(geneFreq),ordered=T),geneFreq=as.vector(geneFreq))
tp100cps<-ggplot(data=geneFreqDf,aes(x=gene,y=geneFreq)) +
geom_bar(stat="identity",fill="steelblue") +
coord_flip() + theme_bw() +
theme(axis.ticks=element_line(color="grey80"),text=element_text(size=20),legend.key.size=unit(1,"cm"),axis.line.x=element_line(colour="black"),panel.grid.major=element_blank(),panel.grid.minor=element_blank(),panel.border=element_blank(),panel.background=element_blank()) +
labs(x="",y="Number of Signatures")
tp100cps