Reads PURPLE somatic CNVs for use with HRDetect.
Value
Tibble containing following columns:
chromosome, start, end
copyNumber (total)
minorAllelePloidy
Examples
x <- system.file("extdata/purple/purple.cnv.somatic.tsv", package = "gpgr")
(cnv <- hrdetect_read_purple_cnv(x))
#> # A tibble: 59 × 5
#> Chromosome chromStart chromEnd total.copy.number.in…¹ minor.copy.number.in…²
#> <chr> <int> <int> <dbl> <dbl>
#> 1 1 1 123605522 1.02 0.0184
#> 2 1 123605523 200044314 1.99 0.989
#> 3 1 200044315 200044570 2.83 0.993
#> 4 1 200044571 248956422 2.01 0.993
#> 5 2 1 93139350 2.01 0.994
#> 6 2 93139351 219955359 2.00 0.996
#> 7 2 219955360 225225069 1.02 0.0196
#> 8 2 225225070 242193529 2.03 0.990
#> 9 3 1 92214015 1.03 0.0176
#> 10 3 92214016 198295559 2.00 0.992
#> # ℹ 49 more rows
#> # ℹ abbreviated names: ¹total.copy.number.inTumour, ²minor.copy.number.inTumour