Plot sexually dimorphic gender marker genes
Source:R/AllGenerics.R
, R/plotGenderMarkers-methods.R
plotGenderMarkers.Rd
This is a convenience function that quickly plots known sexually dimorphic genes, and overall gene experssion for the X and Y chromosomes.
Usage
plotGenderMarkers(object, ...)
# S4 method for bcbioRNASeq
plotGenderMarkers(
object,
normalized = c("tpm", "sf", "fpkm", "vst", "rlog", "tmm", "rle"),
...
)
Arguments
- object
Object.
- normalized
character(1)
orlogical(1)
. Normalization method to apply:FALSE
: Raw counts. When using a tximport-compatible caller, these are length scaled by default (seecountsFromAbundance
argument). When using a featureCounts-compatible caller, these areinteger
.
tximport caller-specific normalizations:
"tpm"
: Transcripts per million.
Additional gene-level-specific normalizations:
TRUE
/"sf"
: Size factor (i.e. library size) normalized counts.
SeeDESeq2::sizeFactors
for details."fpkm"
: Fragments per kilobase per million mapped fragments.
Requiresfast = FALSE
inbcbioRNASeq()
call and gene annotations inrowRanges()
with definedwidth()
.
SeeDESeq2::fpkm()
for details."vst"
: Variance-stabilizing transformation (log2).
Requiresfast = FALSE
to be set duringbcbioRNASeq()
call.
SeeDESeq2::varianceStabilizingTransformation()
for more information."tmm"
: Trimmed mean of M-values.
Calculated on the fly.
SeeedgeR::calcNormFactors()
for details."rle"
: Relative log expression transformation.
Calculated on the fly.
SeerelativeLogExpression()
for details."rlog"
: Deprecated. Regularized log transformation (log2).
No longer calculated automatically duringbcbioRNASeq()
call, but may be defined in legacy objects.
SeeDESeq2::rlog()
for details.
Note that VST is more performant and now recommended by default instead.
Note that
logical(1)
support only applies tocounts()
. Other functions in the package requirecharacter(1)
and usematch.arg()
internally.- ...
Passthrough to
SummarizedExperiment
method defined in AcidPlots. SeeAcidPlots::plotGenderMarkers()
for details.
Examples
data(bcb)
## bcbioRNASeq ====
## Simulate expression of sexually dimorphic gender marker genes.
rownames(bcb)[seq_len(2L)] <- c("ENSMUSG00000086503", "ENSMUSG00000069045")
plotGenderMarkers(bcb)
#> ℹ Using "tpm" counts.
#> ! Failed to map 2 genes: "ENSMUSG00000056673", "ENSMUSG00000068457".
#> → Applying `log2(x + 1L)` transformation.