Nothing
#compares reading in of the three different hap file formats
context("data2haplohh")
test_that("checked_example1", {
sink(file = "test_example1.log")
hh1 <-
data2haplohh(hap_file = "example1.hap",
map_file = "example1.map",
allele_coding = "01")
hh2 <-
data2haplohh(hap_file = "example1.hap",
map_file = "example1.map",
allele_coding = "map")
expect_identical(hh1, hh2)
hh3 <-
data2haplohh(hap_file = "example1.hap",
map_file = "example1.map",
allele_coding = "none")
expect_identical(hh1, hh3)
skip_if_not_installed("vcfR")
hh2 <- data2haplohh(hap_file = "example1.vcf")
expect_identical(hh1, hh2)
sink()
file.remove("test_example1.log")
})
test_that("checked_example2", {
sink(file = "test_example2.log")
hh1 <-
data2haplohh(hap_file = "example2.hap",
map_file = "example2.map",
allele_coding = "01")
hh2 <-
data2haplohh(hap_file = "example2.hap",
map_file = "example2.map",
allele_coding = "map")
expect_identical(hh1, hh2)
skip_if_not_installed("vcfR")
hh2 <- data2haplohh(hap_file = "example2.vcf")
expect_identical(hh1, hh2)
## test with filtering
hh1 <- data2haplohh(
hap_file = "example2.hap",
map_file = "example2.map",
allele_coding = "01",
min_perc_geno.hap = 50,
min_perc_geno.mrk = 50
)
hh2 <-
data2haplohh(
hap_file = "example2.vcf",
min_perc_geno.hap = 50,
min_perc_geno.mrk = 50
)
expect_equivalent(hh1, hh2)
sink()
file.remove("test_example2.log")
})
test_that("checked_bta", {
sink(file = "test_bta.log")
hap1 <- data2haplohh(
hap_file = "bta12_cgu.hap",
map_file = "map.inp",
allele_coding = "map",
chr.name = 12
)
hap2 <-
data2haplohh(
hap_file = "bta12_cgu.thap",
map_file = "map.inp",
haplotype.in.columns = TRUE,
allele_coding = "map",
chr.name = 12
)
#reading standard format includes row-names, reading
#transposed format does not, hence only equivalent, but not equal
expect_equivalent(hap1, hap2)
hap3 <-
data2haplohh(
hap_file = "bta12_hapguess_switch.out",
map_file = "map.inp",
allele_coding = "map",
popsel = 7,
chr.name = 12
)
expect_equivalent(hap1, hap3)
skip_if_not_installed("data.table")
skip_if_not_installed("R.utils")
hap4 <-
data2haplohh(hap_file = "bta12_cgu.vcf.gz",
polarize_vcf = FALSE,
vcf_reader = "data.table")
expect_equal(hap3, hap4)
skip_if_not_installed("vcfR")
hap5 <-
data2haplohh(hap_file = "bta12_cgu.vcf.gz",
polarize_vcf = FALSE,
vcf_reader = "vcfR")
expect_equal(hap3, hap5)
sink()
file.remove("test_bta.log")
})
test_that("data2haplohh_AA_scan", {
skip_if_not_installed("data.table")
skip_if_not_installed("vcfR")
sink(file = "test_AA_scan.log")
tmp <- tempfile()
## check if ancestral allele is correctly parsed
writeLines(
c(
"##fileformat=VCFv4.2",
"##INFO=<ID=AC,Number=A,Type=Integer,Description=\"Total number of alternate alleles\">",
"##INFO=<ID=AA,Number=1,Type=String,Description=\"Ancestral Allele\">",
"##INFO=<ID=VT,Number=.,Type=String,Description=\"Variant Type\">",
"##FORMAT=<ID=GT,Number=1,Type=String,Description=\"Genotype\">",
"#CHROM\tPOS\tID\tREF\tALT\tQUAL\tFILTER\tINFO\tFORMAT\tHG1\tHG2",
"chr1\t10000\trs1\tG\tT\t100\tPASS\tAA=G\tGT\t.\t0|0",
"chr1\t20000\trs2\tG\tA\t100\tPASS\t.\tGT\t0\t1|0",
"chr1\t30000\trs3\tA\tC\t100\tPASS\tAC=2;AF=0.5;AA=C;VT=SNP\tGT\t0\t1|0"
),
tmp
)
hh1 <-
suppressWarnings(data2haplohh(tmp, vcf_reader = "data.table", verbose = FALSE))
hh2 <-
suppressWarnings(data2haplohh(tmp, vcf_reader = "vcfR", verbose = FALSE))
expect_equal(hh1, hh2)
unlink(tmp)
sink()
file.remove("test_AA_scan.log")
})
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