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CellScanner counts microbial species in flow cytometry data of communities separately with the help of a classifier that is trained on mono-cultures.
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msysbio/CellScanner
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CellScanner is a tool that counts different microbial species in flow cytometry data of communities separately with the help of a classifier that is trained on mono-cultures. It is implemented in Python and compatible with Windows, Mac and Linux.
To run CellScanner you first need to get it along with its corresponding dependencies.To this end, you may run the following chunk to get CellScanner and create aconda
environment for it:
git clone https://github.com/msysbio/CellScanner.gitcd CellScannerconda create -n cellscanner python=3.12.2 conda activate cellscannerpip install -r requirements.txt
To run CellScanner with its GUI, you may now run:
# Always remember to activate your conda environment, if you set one for CellScannerconda activate cellscanner# If `python` returns an error message that is not there, try with `python3` insteadpython Cellscanner.py
This will pop-up CellScanner where you can now import your data, fill in your training parameters andpredict your species.
Keep in mind that the CellScanner GUI is a PyQt5 app, meaning it requires from the host to have a working X11 windowing system.
In Windows, you may also follow the steps described above for the Linux and macOS systems.If you try through a WSL however, as already mentioned an X11 is required, which you would have to set up on your own.
Alternatively, you can build an.exe
on your ownAttention! Do not use a WSL. Also, thatpyinstaller
is available.
Then, after you make sure you have activated thecellscanner
conda environment, you may run:
pyinstaller --onefile --icon=logo.ico --add-data"logo.png:." Cellscanner.py
.. or
you can simply download the.exe
of CellScanner v2.0 fromhere.
Assuming you already have CellScanner locally in aconda
environment (seeabove),to run CellScanner using its CLI, you have first to fill in theconfig.yml
file.In this file, you may provide all the arguments you would do in the GUI case as well.
Required arguments are mentioned as such, while it is important to remember that when providing monoculture data for the training step, their names (species_names
in the yaml file) need to be in the same order as their filenames.
species_files:directories: -directory:path:./Testfiles/filenames: -BH_mono_48h_100.fcs -FP_mono_48h_100.fcs -RI_mono_48h_100.fcs -BT_mono_48h_100.fcsspecies_names: -Blautia -Faecalibacterium -Roseburia -Bacteroides
Once your configuration file is ready, you may run CellScanner CLI :
conda activate cellscannerpython CellscannerCLI.py --config config.yml
When using the CLI version, CellScanner is independent of PyQt5, thus no X11 issues should be occurred.
CellScanner v2.0 is based on thefirst version of the tool.
For an overview of what is under the hood, you may have a look on theUser manual of CellScanner v1.0.For the new features that have been added, a manuscript is in process. 📝
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CellScanner counts microbial species in flow cytometry data of communities separately with the help of a classifier that is trained on mono-cultures.