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Hi!
I'm using the function waterfall from GenVisR package.
As the vignette suggests, I want to change the top plot with custom values. However, I cannot find any option to modified these plot.
As you see the below images, top plot seperated 3 kinds of the translational effect. those values cannot be specified and appear in gray as "Undefined".
Q1. Is it possible to customize the Mutation Burden plot ? I want to change the Translational Effect category.
Q2. And I want to know how to decide the Translational Effect (Synonymous, Non Synonymous) by following Mutation type??
If the mutation type is "silent", the translational effect is specified as sysnonymous I think, but I'm not sure if all mutation types except "silent" are designated as nonsynonymous.
The current waterfall() function cannot do this, however I have an improved one (I plan on deprecating this one), that you might be able to get to do what you want.
Specifically the new one can take a coverage argument which is a named vector corresponding to each sample in order to calculate mutation burden. Further you can tell GenVisR to split up these calculations by the mutation type, see plotATally="complex"
Hi!
I'm using the function waterfall from GenVisR package.
As the vignette suggests, I want to change the top plot with custom values. However, I cannot find any option to modified these plot.
As you see the below images, top plot seperated 3 kinds of the translational effect. those values cannot be specified and appear in gray as "Undefined".
[https://stackoverflow.com/questions/49644304/waterfall-plot-genvisr]
Q1. Is it possible to customize the Mutation Burden plot ? I want to change the Translational Effect category.
Q2. And I want to know how to decide the Translational Effect (Synonymous, Non Synonymous) by following Mutation type??
If the mutation type is "silent", the translational effect is specified as sysnonymous I think, but I'm not sure if all mutation types except "silent" are designated as nonsynonymous.
mutationData <- read.table('input5D_Group1.txt', sep='\t', header=TRUE)
Samplelist <- read.table('Samplelist.txt', sep='\t', header=TRUE)
clinicalData <- melt(data=Samplelist, id.vars=c("sample"))
mutation_priority<- c("Missense, Splice site, Nonsense","Frameshift ins/del., Inframe ins/del.", "silent","UTR","Up, Downstream gene variant")
waterfall(mutationData,
fileType = "Custom",
variant_class_order=mutation_priority,
clinData=clinicalData,
clinVarCol=c('Group1'='#5CD1E5'),
mainPalette = c("Missense, Splice site, Nonsense"='#2F9D27',"Frameshift ins/del., Inframe ins/del."='#FF9436',"UTR"='#FF1493',"Up, Downstream gene variant"='#7B68EE'),
sampOrder=Samplelist$sample[Samplelist$group=="Group1"],
plotSamples=Samplelist$sample[Samplelist$group=="Group1"],
rmvSilent=TRUE,
mainDropMut=TRUE,
maxGenes = 1000,
section_heights=c(1, 10, 0.5),
clinLegCol=3,
mainXlabel=TRUE,
coverageSpace=1000000)
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