tests/testthat/test-allele_tests.R
In piyalkarum/rCNV: Detect Copy Number Variants from SNPs Data
test_that("AlleleFreq works", {
expect_type(allele.freq(hetTgen(readVCF(vcf.file.path=paste0(path.package("rCNV"), "/example.raw.vcf.gz")),"GT"),"ind"), "data.frame")
})
piyalkarum/rCNV documentation built on April 17, 2025, 11:46 p.m.
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test_that("AlleleFreq works", {
expect_type(allele.freq(hetTgen(readVCF(vcf.file.path=paste0(path.package("rCNV"), "/example.raw.vcf.gz")),"GT"),"ind"), "data.frame")
})
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Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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