devtools::load_all('/imppc/labs/lplab/share/marc/repos/trackHubeR')
pathHub <- '/imppc/labs/lplab/share/marc/browser/insulinomasHg38'
hubName <- 'insulinomas'
hubShortLabel <- 'insulinomas'
hubLongLabel <- 'insulinomas'
emailAddress <- 'msubirana@igtp.cat'
assemblyDatabase <- 'hg38'
gattacaHtml <- 'http://gattaca.imppc.org/genome_browser/lplab'
gattacaFolderHub <- 'marcHubs'
hubGenerator(pathHub = pathHub,
hubName = hubName,
hubShortLabel = hubShortLabel,
hubLongLabel = hubLongLabel,
emailAddress = emailAddress,
assemblyDatabase = assemblyDatabase,
gattacaHtml = gattacaHtml,
gattacaFolderHub = gattacaFolderHub)
# Delete old trackDb if exists (avoid duplicates in the file)
unlink(file.path(pathHub, assemblyDatabase, 'trackDb.txt')) # put inside trackDb function
# pathBigWig <- '/imppc/labs/lplab/share/marc/browser/parserProve/hg19'
pathVcf <- '/imppc/labs/lplab/share/marc/browser/insulinomasHg38/hg38'
tracksVcf <- list.files(pathVcf,
pattern = "\\.vcf.gz$",
full.names = T)
type <- 'vcfTabix'
visibility <- 'dense'
color <- '0, 0, 0'
# paste(as.vector(col2rgb('blue')), collapse = ",")
# autoScale <- 'on'
for (track in tracksVcf){
trackhubTrack(gattacaHtml = gattacaHtml,
gattacaFolderHub = gattacaFolderHub,
pathHub = pathHub,
track = track,
type = type,
visibility = visibility,
color = color,
autoScale = autoScale)
}
gattacaDir <- '/data/apache/htdocs/genome_browser/lplab'
gattacaUser <- 'msubirana@gattaca'
rsyncHub(gattacaHtml = gattacaHtml,
gattacaDir = gattacaDir,
gattacaFolderHub = gattacaFolderHub,
gattacaUser = gattacaUser)
pathBigWig <- '/imppc/labs/lplab/share/marc/browser/insulinomasHg38/hg38'
tracksigWigAtac <- list.files(pathBigWig,
pattern = "\\ATAC.bw$",
full.names = T)
type <- 'bigWig'
visibility <- 'full'
color <- '255, 204, 153'
autoScale <- 'on'
for (track in tracksigWigAtac){
trackhubTrack(gattacaHtml = gattacaHtml,
gattacaFolderHub = gattacaFolderHub,
pathHub = pathHub,
track = track,
type = type,
visibility = visibility,
color = color,
autoScale = autoScale)
}
tracksigWigChip <- list.files(pathBigWig,
pattern = "\\ChIP.bw$",
full.names = T)
type <- 'bigWig'
visibility <- 'full'
color <- '153, 204, 255'
autoScale <- 'on'
for (track in tracksigWigChip){
trackhubTrack(gattacaHtml = gattacaHtml,
gattacaFolderHub = gattacaFolderHub,
pathHub = pathHub,
track = track,
type = type,
visibility = visibility,
color = color,
autoScale = autoScale)
}
gattacaDir <- '/data/apache/htdocs/genome_browser/lplab'
gattacaUser <- 'msubirana@gattaca'
rsyncHub(gattacaHtml = gattacaHtml,
gattacaDir = gattacaDir,
gattacaFolderHub = gattacaFolderHub,
gattacaUser = gattacaUser)
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