View source: R/cytof_preProcess.R
cytof_exprsMerge | R Documentation |
Apply preprocessing on each FCS file including compensation (for FCM data only) and transformation
with selected markers, then expression matrix are extracted and merged using one of the methods,
all
, min
, fixed
or ceil
cytof_exprsMerge( fcsFiles, comp = FALSE, transformMethod = c("autoLgcl", "cytofAsinh", "logicle", "arcsinh", "none"), scaleTo = NULL, markers = NULL, mergeMethod = c("ceil", "all", "fixed", "min"), fixedNum = 10000, sampleSeed = 123, ... )
fcsFiles |
A vector of FCS file names. |
comp |
If |
transformMethod |
Data Transformation method, including |
scaleTo |
Scale the expression to a specified range c(a, b), default is NULL. |
markers |
It can be either a text file that containing markers to be used for analysis or a vector of the marker names. |
mergeMethod |
Merge method for mutiple FCS expression data. cells can be combined using one of the four different methods including |
fixedNum |
The fixed number of cells to be extracted from each FCS file. |
sampleSeed |
A sampling seed for reproducible expression matrix merging. |
... |
Other arguments passed to |
A matrix containing the merged expression data, with selected markers, row names added as filename_cellID
, column names added as name<desc>
.
cytof_exprsExtract
d<-system.file('extdata',package='cytofkit2') fcsFiles <- list.files(d,pattern='.fcs$',full=TRUE) merged <- cytof_exprsMerge(fcsFiles)
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