library(TrenaValidator)
library(BiocParallel)
if(!exists("tbl.benchmark"))
tbl.benchmark <- get(load(system.file(package="TrenaValidator", "extdata", "tbl.A.RData")))
mtx <- get(load(system.file(package="TrenaValidator", "extdata", "mtx.gtex.lung.RData")))
OUT_DIR <- "lung-eliteGH"
LOG_DIR <- "lung-eliteGH.log"
if(!file.exists(OUT_DIR))
dir.create(OUT_DIR)
if(!file.exists(LOG_DIR))
dir.create(LOG_DIR)
#------------------------------------------------------------------------------------------------------------------------
# steps:
# get enhancers for targetGene
# get high-scoring TFs in highly conserved regions of the enhancers
# build trena model with those tfs and a GTEX expression matrix
# save enhancers, motif matches, model
validateOnePair <- function(TF, targetGene)
{
printf("--- validateOnePair(%s, %s)", TF, targetGene)
tv <- TrenaValidator(TF, targetGene, mtx, tbl.benchmark)
findEnhancers(tv, eliteOnly=TRUE)
tbl.enhancers <- getEnhancerTable(tv)
save(tbl.enhancers, file=sprintf("%s/%s-%s.RData", OUT_DIR, TF, targetGene))
} # validateOnePair
#------------------------------------------------------------------------------------------------------------------------
WORKERS <- 2
parallel <- TRUE
rows <- sample(seq_len(nrow(tbl.benchmark)),3)
if(parallel){
bp.params <- MulticoreParam(stop.on.error=FALSE, log=TRUE, logdir=LOG_DIR, threshold="INFO", workers=WORKERS)
results <- bptry({bplapply(rows,
function(r) with(tbl.benchmark[r,], validateOnePair(TF, target)),
BPPARAM=bp.params)})
} else {
results <- lapply(rows, function(r) with(tbl.benchmark[r,], validateOnePair(TF, target)))
}
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