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I am trying to generate some rainfall plots from somatic variants over chromosomes. I tested my code on a table generated from somatic SNVs and that works fine. However, I later noticed that kpPlotRainfall also takes a path to VCF as data, I tried that with VCF which contains more complex variants like indels, duplications, and BNDs, and I got the following error:
Error in `[[<-`(`*tmp*`, name, value = c(`NA` = "#888888")) :
1 elements in value to replace 0 elements
Calls: kpPlotRainfall -> $<- -> $<- -> [[<- -> [[<-
Execution halted
I am using custom genome and tracks (chm13), and generating the plots for each chromosome on a PDF page. This works fine when the data given to kpPlotRainfall is a GRanges object, but not when giving a VCF
# genome size and bands for chm13 t2tsample="sample1"custom.genome<- toGRanges(genome_size)
custom.cytobands<- toGRanges(genome_bands)
chromosomes= c("chr1")
i<-1
pdf("test.pdf", height=10, width=16)
# this is supposed to be part of a loop that plots for each chromosomekp<- plotKaryotype(plot.type=1, genome=custom.genome[seqnames(custom.genome)==chromosomes[i]]
,cytobands=custom.cytobands[seqnames(custom.cytobands)==chromosomes[i]],
chromosome=chromosomes[i])
kpAddCytobandLabels(kp, force.all=TRUE, srt=90, col='orange')
title= paste0("[vcf] Somatic Mutations of ", sample, " and chromosome ", chromosomes[i])
kpAddMainTitle(kp, main=title, cex=1.5)
kpAddBaseNumbers(kp)
# only chromosome one VCF
kpPlotRainfall(kp, data="sniffles_svs_chr1.vcf")
kpAxis(kp, ymax=8, r0=0.01, r1=0.9)
kpAddLabels(kp, labels= c("Distance between mutations (log10)"), srt=90, pos=1, label.margin=0.04,
r0=0.01, r1=0.9)
dev.off()
To debug this, I kept removing different SVs (e.g. DEL, INS, INV, DUP, BND), until it worked with only SNVs left.
Is this the intended usage? Or am I doing something wrong?
Thanks for the help,
Fawaz
The text was updated successfully, but these errors were encountered:
Hi,
Thanks for the great library!
I am trying to generate some rainfall plots from somatic variants over chromosomes. I tested my code on a table generated from somatic SNVs and that works fine. However, I later noticed that kpPlotRainfall also takes a path to VCF as data, I tried that with VCF which contains more complex variants like indels, duplications, and BNDs, and I got the following error:
I am using custom genome and tracks (chm13), and generating the plots for each chromosome on a PDF page. This works fine when the data given to
kpPlotRainfall
is a GRanges object, but not when giving a VCFTo debug this, I kept removing different SVs (e.g. DEL, INS, INV, DUP, BND), until it worked with only SNVs left.
Is this the intended usage? Or am I doing something wrong?
Thanks for the help,
Fawaz
The text was updated successfully, but these errors were encountered: