Nothing
library(scPloidy)
test_that("fragmentoverlapcount works", {
skip_if_not_installed("GenomicRanges")
skip_if_not_installed("IRanges")
skip_if_not_installed("readr")
library(GenomicRanges)
library(IRanges)
library(readr)
targetregions =
GenomicRanges::GRanges(
c("chr19", "chr20"),
IRanges::IRanges(c(1, 1), width = 500000000))
simpleRepeat = readr::read_tsv(
test_path("testdata/simpleRepeat.chr19_20.txt.gz"),
col_names = c("chrom", "chromStart", "chromEnd"))
simpleRepeat[, 2:3] = simpleRepeat[, 2:3] + 1 # convert from 0-based position to 1-based
simpleRepeat = GenomicRanges::makeGRangesFromDataFrame(
as.data.frame(simpleRepeat),
seqnames.field = "chrom",
start.field = "chromStart",
end.field = "chromEnd")
load(test_path("testdata/SHR_m154211.10cells.chr19_20.result.RData"))
expect_identical(
fragmentoverlapcount(
test_path("testdata/SHR_m154211.10cells.chr19_20.fragments.txt.gz"),
targetregions,
excluderegions = simpleRepeat,
Tn5offset = c(0, -9))[, 1:8],
resfragmentoverlapcount)
})
test_that("ploidy works", {
load(test_path("testdata/SHR_m154211.fragmentoverlap.RData"))
resploidy = read.table(
test_path("testdata/SHR_m154211.result.txt"),
header = TRUE)
expect_equal(
ploidy(fragmentoverlap,
c(2, 4, 8)),
resploidy)
})
test_that("cnv works", {
data(GSE129785_SU008_Tumor_Pre)
x = cnv(SU008_Tumor_Pre_fragmentoverlap,
SU008_Tumor_Pre_windowcovariates,
levels = c(2, 4),
deltaBICthreshold = -600)
expect_equal(
x$CNV,
rescnv$CNV)
expect_equal(
x$cellwindowCN,
rescnv$cellwindowCN)
})
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