View source: R/flowCytometryFunctions.R
process_fcs | R Documentation |
process_fcs
uses mixture models to cluster bacteria from background
debris and fits a linear model to SSC-H vs SSC-A to remove doublets.
process_fcs(fcs_file, flu_channels = c("BL1-H"), do_plot = F, pre_cleaned = F)
fcs_file |
path of an .fcs files to be processed. |
flu_channels |
a vector of strings of the fluorescence channels to keep in the processed data and plotting. Defaults to "BL1-H". |
do_plot |
a Boolean flag to determine whether to produce plots showing
the trimming of each |
pre_cleaned |
have you pre removed background debris. |
nothing is returned. A processed .fcs file is produced and a plot if
do_plot = TRUE
.
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