#----Load data------------------------------------------------------------------
data(tx2gene)
data(sample_info)
sample_info <- rbind(
sample_info, sample_info
)
sample_info$BioSample[2] <- "SAMN02422670"
sample_info$Experiment[2] <- "SRX384346"
sample_info$BioProject[2] <- "PRJNA229999"
sample_info$Run[2] <- "SRR1039509"
sample_info$Layout[2] <- "SINGLE"
## Create fake single-end FASTQ file
fake_fastq <- c(
"@SRR1039508.2486",
"TTCAACCTTTCATGTAACAAAACTTATAAAATTCCTTTAGCTCTTCCTTTTTCTAAAGAAAAA",
"+",
"HJJJJJJJJJJJJJJJJJJJJJJJJJJIJJJJJJJJJJJJJJJJJJJJJJJJJJJIJJJJJJJ",
"@SRR1039508.14392",
"CTGGCACACCTGATCAAATTTCTCCTCCATCAAGTCTCTGCAACACCGGCTCTCCACCAGGGT",
"+",
"HJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJIJGIJJHHHHFFFFFDDD;",
"@SRR1039508.14861",
"GACATTACTTTCACTTGTGTTTCATATTCCGTAAAACGAACAAAGCCAAACCCCTTTGAATGA",
"+",
"HJJJJJJJJJJJJJJJJHHIJJJJJJJJJIJJIJIJJJJJJJJJJJJJJJIAHHHHFFFFFFF",
"@SRR1039508.18596",
"AGCGGCCAGATCGGCTTCATGCTGTGCAGCAAGAACCCGAGCACGAACTTCCAGGAGCCGGTG",
"+",
"HJJJJJJJJJJJJJJJJI>FGGGEBFB<CF@HGFHADHEEEFDED@BB<C@CCCDBBBD9@;@",
"@SRR1039508.25193",
"TCATACACTGAGACACTGGATTCCTGTAGCGAAGCCCACACGCCCCTGGAAACTGGGCTGTAA",
"+"
)
fastqdir <- file.path(tempdir(), "fastqdir")
if(!dir.exists(fastqdir)) { dir.create(fastqdir, recursive = TRUE) }
## Write fake FASTQ to `fastqdir`
gz1 <- gzfile(file.path(fastqdir, "SRR1039509.fastq.gz"), "w")
writeLines(text = fake_fastq, con = gz1)
close(gz1)
## Copy FASTQ files in inst/extdata to `fastqdir`
fqfiles <- list.files(
system.file("extdata", package = "bears"), pattern = ".fastq.gz",
full.names = TRUE
)
c1 <- file.copy(from = fqfiles[1], to = fastqdir)
c2 <- file.copy(from = fqfiles[2], to = fastqdir)
# Path to files and directories used in this set of tests
salmonindex <- file.path(tempdir(), "salmonidx")
transcriptome_path <- system.file(
"extdata", "Homo_sapiens.GRCh37.75_subset_transcripts.fa.gz",
package = "bears"
)
salmondir <- file.path(tempdir(), "salmon_quant")
## Create a random SummarizedExperiment object
nrows <- 200
ncols <- 6
counts <- matrix(runif(nrows * ncols, 1, 1e4), nrows)
colData <- data.frame(
Treatment=rep(c("ChIP", "Input"), 3),
row.names=LETTERS[1:6]
)
se_random <- SummarizedExperiment::SummarizedExperiment(
assays = list(counts = counts), colData = colData
)
## Change PATH
Sys.setenv(
PATH = paste(
Sys.getenv("PATH"),
paste0(Sys.getenv("HOME"), "/.local/bin"),
paste0(
Sys.getenv("HOME"),
"/Documents/Programs/salmon-1.9.0_linux_x86_64/bin/"
),
"/opt/STAR-2.7.9a/bin/Linux_x86_64_static/",
"/opt/salmon-1.9.0_linux_x86_64/bin/",
"/opt/bin/",
"/opt/kallisto/",
"/opt/subread-2.0.3-Linux-x86_64/bin/",
"/opt/stringtie-2.1.7.Linux_x86_64/",
"/opt/taco-v0.7.3.Linux_x86_64/",
sep = ":"
)
)
#----Start tests----------------------------------------------------------------
test_that("salmon_index(), salmon_quantify(), and salmon2se() work", {
si <- data.frame()
sq <- data.frame()
se_gene <- se_random
se_tx <- se_random
se_both <- list()
if(salmon_is_installed()) {
si <- salmon_index(salmonindex, transcriptome_path)
sq <- salmon_quantify(
sample_info, fastqdir, salmonindex, salmondir
)
d <- fs::dir_delete(file.path(salmondir, "SAMN02422670"))
se_gene <- salmon2se(sample_info[1, ], "gene", salmondir, tx2gene)
se_tx <- salmon2se(sample_info[1, ], "transcript", salmondir, tx2gene)
se_both <- salmon2se(sample_info[1, ], "both", salmondir, tx2gene)
expect_error(
salmon2se(sample_info[1, ], "error", salmondir, tx2gene)
)
}
expect_equal(class(si), "data.frame")
expect_equal(class(sq), "data.frame")
expect_true("SummarizedExperiment" %in% class(se_gene))
expect_true("SummarizedExperiment" %in% class(se_tx))
expect_equal(class(se_both), "list")
})
test_that("run2biosample_salmon() handles technical replicates", {
r1 <- run2biosample_salmon(sample_info, fastqdir)
expect_equal(class(r1), "list")
expect_equal(length(r1), 2)
expect_equal(names(r1), c("paired", "single"))
})
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