QCplots | R Documentation |
Correlation plots default to mRNA covering reads.
Meta plots defaults to leader, cds, trailer.
Output will be stored in same folder as the
libraries in df.
Correlation plots will be fpkm correlation and
log2(fpkm + 1) correlation between samples.
QCplots(
df,
region = "mrna",
stats_folder = QCfolder(df),
plot.ext = ".pdf",
complex.correlation.plots = TRUE,
library.names = bamVarName(df),
force = TRUE,
BPPARAM
)
df |
an ORFik |
region |
a character (default: mrna), make raw count matrices of whole mrnas or one of (leaders, cds, trailers) |
stats_folder |
directory to save, default:
|
plot.ext |
character, default: ".pdf". Alternatives: ".png" or ".jpg". Note that in pdf format the complex correlation plots become very slow to load! |
complex.correlation.plots |
logical, default TRUE. Add in addition to simple correlation plot two computationally heavy dots + correlation plots. Useful for deeper analysis, but takes longer time to run, especially on low-quality gpu computers. Set to FALSE to skip these. |
library.names |
character vector, names of libraries, default: name_decider(df, naming) |
force |
logical, default TRUE If TRUE, reload library files even if
matching named variables are found in environment used by experiment
(see |
BPPARAM |
how many cores/threads to use? default: bpparam().
To see number of threads used, do |
Is part of QCreport
invisible(NULL) (objects stored to disc)
Other QC report:
QCreport()
,
QCstats()
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