library(shiny)
library(igvShiny)
library(cyjShiny)
library(GenomicAlignments)
#cyjshiny object
tbl.nodes <- data.frame(id=c("A", "B", "C"),
type=c("kinase", "TF", "glycoprotein"),
lfc=c(-3, 1, 1),
count=c(0, 0, 0),
stringsAsFactors=FALSE)
tbl.edges <- data.frame(source=c("A", "B", "C"),
target=c("B", "C", "A"),
interaction=c("phosphorylates", "synthetic lethal", "unknown"),
stringsAsFactors=FALSE)
graph.json <- toJSON(dataFramesToJSON(tbl.edges, tbl.nodes), auto_unbox=TRUE)
#----------------------------------------------------------------------------------------------------
f <- system.file(package="igvShiny", "extdata", "gwas.RData")
stopifnot(file.exists(f))
tbl.gwas <- get(load(f))
print(dim(tbl.gwas))
printf <- function(...) print(noquote(sprintf(...)))
ns.sep <- "."
#----------------------------------------------------------------------------------------------------
igv_ui = function(id){
ns <- NS(id)
shinyUI(fluidPage(
igvShinyOutput(ns('igvShiny_0')),
cyjShiny::cyjShinyOutput(ns('cyjShiny')),
width=10
)
)
}
#----------------------------------------------------------------------------------------------------
igv_server <- function(input, output, session) {
ns <- session$ns
genomes <- c("hg38", "hg19", "mm10", "tair10", "rhos")
loci <- c("chr5:88,466,402-89,135,305", "MEF2C", "Mef2c", "1:7,432,931-7,440,395", "NC_007494.2:370,757-378,078")
i <- 2
output$igvShiny_0 <- renderIgvShiny({
genomeOptions <-
parseAndValidateGenomeSpec(genomeName = genomes[i], initialLocus = loci[i])
igvShiny(genomeOptions, displayMode = "SQUISHED")
})
output$cyjShiny <- cyjShiny::renderCyjShiny({
cyjShiny::cyjShiny(graph=graph.json, layoutName="cola")
})
} # server
#----------------------------------------------------------------------------------------------------
server <- function(input, output, session){
callModule(igv_server, "igv")
}
ui <- fluidPage(
igv_ui(id="igv")
)
runApp(shinyApp(ui = ui, server = server), port=9834)
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