plotCoverage(x, geneID = NULL, geneName = NULL, eventID = NULL,
which = NULL, sample_info = NULL, sizefactor = NA, toscale = c("exon",
"none", "gene"), color = "darkblue", ylim = NULL, label = NULL,
nbin = 200, summary = mean, curvature = 1, main = NULL,
min_anchor = 1, cores = 1)SGFeatureCounts or SGFeatures object.
If x is an SGFeatureCounts object that includes
multiple samples, average coverage and splice junction counts
are obtained.xxxGRanges used to subset xx is an SGFeatureCounts object, sample information
is obtained from colData(x). If sample_info includes
multiple samples, average coverage and splice junction counts
are obtained.sample_info. Used to scale coverages and splice
junction counts before plotting, or before averaging across samples.
Set to NA to disable scaling. If NULL, size factors
are calculated as the number of bases sequenced (the product of library
size and average number of bases sequenced per read or fragment),
plotted coverages and splice junction counts are per 1 billion
sequenced bases.data.frame with information on splice junctions included
in the splice graphpar(mfrow = c(4, 1))
for (j in seq_len(4)) plotCoverage(sgfc_pred[, j])
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