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An R package for the processing of plate reader and flow cytometry data. This includes: normalisation and calibration of plate reader data, and removing debris and doublets and calibration of flow cytometry data.

License: GNU General Public License v3.0

R 100.00%
calibration flow-cytometry fluorescence microplate-reader normalisation plate-reader

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flopr's Issues

process_fcs() : Error 'x' must be an object of class flowFrame

I'm trying to use flopR to analyze a few .fcs files for the automated features it provides. I have installed the package using devtools::install_github() and ensured the prerequisites c("flowCore", "flowClust", "flowStats") are installed.

When I try to run one .fcs file at a time from the dataset using process_fcs(_fcspath_, flu_channels = 'mScarlet-I-A', do_plot = T)

I get the output -

[1] "2 clusters found"
[1] "only debris found"
Error 'x' must be an object of class flowFrame

and some additional warning messages reg NaNs and fluorescent channel exceeding saturation

How do I go about troubleshooting this since no additional information is given about the function generating the error?

I am able to read and visualize the same files using flowWorkspace::'s cytoset and cytoframe datatypes like this -
image

The .fcs file is attached here -
E01.zip

Desktop:

  • OS: Windows 10
  • R Version : 4.1

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