library(methods)
suppressPackageStartupMessages(library(GetoptLong))
chr = "chr18"
peak = NULL
GetoptLong("chr=s", "chromosome",
"peak=s@", "peak name")
BASE_DIR = "/icgc/dkfzlsdf/analysis/B080/guz/roadmap_analysis/re_analysis"
source(qq("@{BASE_DIR}/scripts/configure/roadmap_configure.R"))
if(is.null(peak)) peak = MARKS
neg_cr = readRDS(qq("@{OUTPUT_DIR}/rds/all_neg_cr_w6s3.rds"))
pos_cr = readRDS(qq("@{OUTPUT_DIR}/rds/all_pos_cr_w6s3.rds"))
cr = c(neg_cr, pos_cr)
cr = cr[cr$corr_fdr < 0.05 & cr$meth_anova_fdr < 0.05 & cr$meth_diameter > 0.1]
cr = copy_cr_attribute(neg_cr, cr)
if(!chr %in% unique(as.character(seqnames(cr)))) {
stop("'chr' does not exist in 'cr'.")
}
dir.create(qq("@{OUTPUT_DIR}/gviz/@{chr}"), showWarnings = FALSE)
if(length(peak) > 0) {
if(!all(peak %in% MARKS)) {
stop("'peak' should all be in 'MARKS'.")
}
peak_list = lapply(peak, get_peak_list)
names(peak_list) = peak
}
cr_subset = cr[seqnames(cr) == chr]
gn = epic::extract_field_from_gencode(GTF_FILE, level = "gene", primary_key = "gene_id", field = "gene_name")
for(gi in unique(cr_subset$gene_id)) {
pdf(qq("@{OUTPUT_DIR}/gviz/@{chr}/gviz_@{chr}_@{gi}_@{gn[gi]}.pdf"), width = 12, height = 6 + 1*length(peak))
# try(
cr_gviz(cr_subset, gi, EXPR, TXDB,
gf_list = list(CGI = CGI),
hm_list = peak_list, symbol = gn[gi])
# )
dev.off()
}
# for(chr in paste0("chr", 1:22)) {
# cmd = qq("Rscript-3.3.0 /icgc/dkfzlsdf/analysis/B080/guz/roadmap_analysis/re_analysis/scripts/04.correlated_regions_gviz.R --chr @{chr}")
# cmd = qq("perl /home/guz/project/development/ngspipeline2/qsub_single_line.pl '-l walltime=40:00:00,mem=15G -N cr_gviz_@{chr}' '@{cmd}'")
# system(cmd)
# }
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