Nothing
# detach(package:vcfR, unload=T)
#
library(testthat)
library(vcfR)
context("freq_peak_plot")
#data("vcfR_example")
test_that("freq_peak_plot works, empty plot",{
expect_true(is.null(freq_peak_plot(pos=1:40)))
})
test_that("freq_peak_plot works, pinfsc50 plot",{
data(vcfR_example)
gt <- extract.gt(vcf)
hets <- is_het(gt)
# Censor non-heterozygous positions.
is.na(vcf@gt[,-1][!hets]) <- TRUE
# Extract allele depths.
ad <- extract.gt(vcf, element = "AD")
ad1 <- masplit(ad, record = 1)
ad2 <- masplit(ad, record = 2)
freq1 <- ad1/(ad1+ad2)
freq2 <- ad2/(ad1+ad2)
myPeaks1 <- freq_peak(freq1, getPOS(vcf))
is.na(myPeaks1$peaks[myPeaks1$counts < 20]) <- TRUE
myPeaks2 <- freq_peak(freq2, getPOS(vcf), lhs = FALSE)
is.na(myPeaks2$peaks[myPeaks2$counts < 20]) <- TRUE
hopefully_null <- freq_peak_plot(pos = getPOS(vcf), ab1 = freq1, ab2 = freq2, fp1 = myPeaks1, fp2=myPeaks2)
expect_true(is.null(hopefully_null))
})
test_that("freq_peak_plot works, pinfsc50 mySamp works",{
data(vcfR_example)
gt <- extract.gt(vcf)
hets <- is_het(gt)
# Censor non-heterozygous positions.
is.na(vcf@gt[,-1][!hets]) <- TRUE
# Extract allele depths.
ad <- extract.gt(vcf, element = "AD")
ad1 <- masplit(ad, record = 1)
ad2 <- masplit(ad, record = 2)
freq1 <- ad1/(ad1+ad2)
freq2 <- ad2/(ad1+ad2)
myPeaks1 <- freq_peak(freq1, getPOS(vcf))
is.na(myPeaks1$peaks[myPeaks1$counts < 20]) <- TRUE
myPeaks2 <- freq_peak(freq2, getPOS(vcf), lhs = FALSE)
is.na(myPeaks2$peaks[myPeaks2$counts < 20]) <- TRUE
i <- 3
hopefully_null <- freq_peak_plot(pos = getPOS(vcf), ab1 = freq1, ab2 = freq2,
fp1 = myPeaks1, fp2=myPeaks2, mySamp = i)
expect_true(is.null(hopefully_null))
})
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