test_that("test_readBed", {
bedHg19Fn <- file.path(system.file("extdata", package="CNEr"),
"filter_regions.hg38.bed")
bedHg19 <- readBed(bedHg19Fn)
## Chekc the number of items
expect_identical(length(bedHg19), 413L)
## Check the first 5 ranges
expect_identical(start(bedHg19[1:5]),
as.integer(c(26817474, 156772018, 156772160,
156772495, 156774135)))
}
)
test_that("test_axtInfo", {
axtFilesHg19DanRer7 <- file.path(system.file("extdata", package="CNEr"),
"hg38.danRer10.net.axt")
axtInfoHg19DanRer7 <- axtInfo(axtFilesHg19DanRer7)
## Check the number of alignments
expect_identical(length(axtInfoHg19DanRer7), 50L)
## Check the first five widths of alignments
expect_identical(axtInfoHg19DanRer7[1:5], c(359L, 398L, 961L, 673L, 55L))
}
)
test_that("test_readAxt", {
axtFilesHg19DanRer7 <- file.path(system.file("extdata", package="CNEr"),
"hg38.danRer10.net.axt")
axtHg19DanRer7 <- readAxt(axtFilesHg19DanRer7)
## Check the number of alignments
expect_identical(length(axtHg19DanRer7), 50L)
## Check the target ranges
library(GenomicRanges)
ansTargetsRanges <- GRanges(seqnames=c("chr1", "chr1", "chr10", "chr13",
"chr13"),
ranges=IRanges(start=c(148165963, 222131480,
65322021,
94750629, 94966940),
end=c(148166304, 222131835,
65322919,
94751259, 94966991)),
strand="+")
expect_identical(as.character(seqnames(targetRanges(axtHg19DanRer7)[1:5])),
as.character(seqnames(ansTargetsRanges)))
expect_identical(ranges(targetRanges(axtHg19DanRer7)[1:5]),
ranges(ansTargetsRanges))
expect_identical(strand(targetRanges(axtHg19DanRer7)[1:5]),
strand(ansTargetsRanges))
## Check the query ranges
ansQueryRanges <- GRanges(seqnames=c("chr6"),
ranges=IRanges(start=c(25825774, 24819722,
26227619, 26600600,
26745445),
end=c(25826099, 24820074, 26228468,
26601208, 26745499)),
strand=c("+"))
expect_identical(as.character(seqnames(queryRanges(axtHg19DanRer7)[1:5])),
as.character(seqnames(ansQueryRanges)))
expect_identical(ranges(queryRanges(axtHg19DanRer7)[1:5]),
ranges(ansQueryRanges))
expect_identical(strand(queryRanges(axtHg19DanRer7)[1:5]),
strand(ansQueryRanges))
## Check the score
expect_identical(score(axtHg19DanRer7)[1:5],
c(5310L, 221L, 946L, 3302L, 711L))
library(Biostrings)
## Check the target seqs
expect_equivalent(subseq(targetSeqs(axtHg19DanRer7)[1:5], start=1, end=5),
DNAStringSet(c("TCTCT", "CTTAA", "TTGCA", "GCCTT",
"ATTCA"))
)
## Check the query seqs
expect_equivalent(subseq(querySeqs(axtHg19DanRer7)[1:5], start=1, end=5),
DNAStringSet(c("TTTCT", "TTCGA", "TTGTT", "GCTTT",
"AGCCA"))
)
}
)
test_that("test_writeAxt", {
axtFilesHg19DanRer7 <- file.path(system.file("extdata", package="CNEr"),
"hg38.danRer10.net.axt")
axtHg19DanRer7 <- readAxt(axtFilesHg19DanRer7)
## Check we can output the axt
expect_silent(writeAxt(axtHg19DanRer7, con=tempfile()))
})
test_that("test_read.rmMask.GRanges", {
fn <- system.file("extdata", "ce2chrM.fa.out", package="IRanges")
ans <- read.rmMask.GRanges(fn)
## Check the number of repeats
expect_identical(length(ans), 28L)
})
test_that("test_readCNERangesFromSQLite", {
dbName <- file.path(system.file("extdata", package="CNEr"),
"danRer10CNE.sqlite")
cneGRangePairs <- readCNERangesFromSQLite(dbName=dbName,
tableName="danRer10_hg38_45_50")
expect_equal(length(cneGRangePairs), 3209L)
})
test_that("test_read.rmskFasta", {
library(GenomicRanges)
fn <- file.path(system.file("extdata", package="CNEr"),
"rmsk.fa")
ans <- read.rmskFasta(fn)
expect_equal(ans, GRanges(seqnames=c("chr1", "chr2"),
ranges=IRanges(start=c(6,3),
end=c(7,5)),
strand="+"))
})
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.