test_checkVariantConcordance <- function() {
p53 <- gmapR:::exonsOnTP53Genome("TP53")
bams <- LungCancerLines::LungCancerBamFiles()
bam <- bams$H1993
tally.param <- VariantTallyParam(gmapR::TP53Genome(),
readlen = 100L,
high_base_quality = 23L,
which = range(p53))
called.variants <- callVariants(bam, tally.param)
concord <- checkVariantConcordance(called.variants,
called.variants)
checkTrue(1L, concord$fraction)
}
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