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### =========================================================================
### Tests for bedtools genomecov command
### -------------------------------------------------------------------------
###
### Based on tests from bedtools (C) 2016 Aaron Quinlan et al.
###
test_genomecov <- function() {
setwd(system.file("unitTests", "data", "genomecov", package="HelloRanges"))
genome <- import("test.genome")
y <- import("y.bed", genome=genome)
cov_gr <- as(coverage(granges(y)), "GRanges")
exp <- subset(cov_gr, score > 0L)
r <- bedtools_genomecov("-i y.bed -bg -g test.genome")
checkIdentical(exp, eval(r))
asBam("three_blocks.sam", "three_blocks", overwrite=TRUE)
three_blocks <- import("three_blocks.bam")
cov_gr <- as(coverage(granges(three_blocks)), "GRanges")
exp <- subset(cov_gr, score > 0L)
r <- bedtools_genomecov("-i three_blocks.bam -bg")
checkIdentical(exp, eval(r))
cov_gr <- as(coverage(three_blocks), "GRanges")
exp <- subset(cov_gr, score > 0L)
r <- bedtools_genomecov("-i three_blocks.bam -bg -split")
checkIdentical(exp, eval(r))
exp <- cov_gr
r <- bedtools_genomecov("-i three_blocks.bam -bga -split")
checkIdentical(exp, eval(r))
exp <- GPos(coverage(three_blocks))
r <- bedtools_genomecov("-i three_blocks.bam -dz -split")
checkIdentical(exp, eval(r))
asBam("sam-w-del.sam", "sam-w-del", overwrite=TRUE)
sam_w_del <- import("sam-w-del.bam")
cov_gr <- as(coverage(sam_w_del, drop.D.ranges=TRUE), "GRanges")
exp <- subset(cov_gr, score > 0L)
r <- bedtools_genomecov("-i sam-w-del.bam -bg -split")
checkIdentical(exp, eval(r))
exp <- DataFrame(seqnames=Rle(c("1", "2", "3", "genome"),
c(3L, 1L, 1L, 3L)),
coverage = factor(c(0:2, 0, 0, 0:2)),
count = c(93, 4, 3, rep(100, 2), 293, 4, 3),
len = c(rep(100, 5), rep(300, 3)))
exp <- within(exp, fraction <- count / len)
r <- bedtools_genomecov("-i y.bam")
checkIdentical(exp, eval(r))
asBam("pair-chip.sam", "pair-chip", overwrite=TRUE)
pair_chip <- import("pair-chip.bam", paired=TRUE)
cov_gr <- as(coverage(granges(pair_chip)), "GRanges")
exp <- subset(cov_gr, score > 0L)
r <- bedtools_genomecov("-i pair-chip.bam -bg -pc")
checkIdentical(exp, eval(r))
asBam("chip.sam", "chip", overwrite=TRUE)
chip <- import("chip.bam")
cov_gr <- as(coverage(resize(granges(chip), 100L)), "GRanges")
exp <- subset(cov_gr, score > 0L)
r <- bedtools_genomecov("-i chip.bam -bg -fs 100")
checkIdentical(exp, eval(r))
}
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