Description Usage Arguments Value Examples
View source: R/plotGeneModel.R
plotGeneModel
Given a gff file and snpeff annotated snp file,
plot the mutations pertaining to a specific gene.
1 2 3 4 5 6 7 | plotGeneModel(gff, snpEffVCF, geneID, upstreamBuffer = 1000,
downstreamBuffer = 500, features2plot = c("exon", "five_prime_UTR",
"three_prime_UTR"), colors = c("steelblue3", "lightsteelblue1",
"lightsteelblue1"), mutations2annotate = c("missense", "stop", "start"),
pchMutation = c(2, 8, 8), colMutation = c("darkblue", "darkred", "green"),
orientation = NULL, windowSize = 100, stepSize = 10, scaleBar = 0.1,
...)
|
gff |
The gff file, must contain the following column names: chr, type, start, end, orientation, info |
snpEffVCF |
The snpeff annotated vcf file, must contain the following column names: CHR, POS, INFO, where info is the snpeff annotations |
upstreamBuffer |
How many bp upstream should be plotted |
downstreamBuffer |
How many bp downstream should be plotted |
features2plot |
What gff elements should be plotted? |
colors |
Colors for exon, 3'UTR and 5'UTR respectively |
mutations2annotate |
Partial string matching for types of differences to annotate |
pchMutation |
Shape of points that specify annotated sites |
colMutation |
Color of points that specify annotated sites |
windowSize |
Sliding window (for difference densities) window size |
stepSize |
Sliding window step size |
scaleBar |
If NULL, do not plot a scale bar, otherwise, specify the proportion of total gene space that the scale bar covers |
... |
additional arguments, not currently in use. |
a dataframe containing the annotated vcf file of Hal2 Fil2 differences for the gene specified in geneID
1 | plotGeneModel(gff = gf, snpEffVCF = sev, geneID = "Pahal.C00786", windowSize=200, stepSize = 5)
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