Open gabrielpan147 opened 10 months ago
Hi Gabriel, we also faced that issue recently. I couldn't find a solution yet, but are working on it. If you find a solution in the meanwhile, please let me know, maybe yours is better than mine.
Hello, thanks for your reply! Actually I did not find any current packages in R which support FCS3.2. I don't know if there are tools that can easily convert FCS3.1 into FCS3.2, I will take a look at FCS3.2 standard when I have time and see if we can do it by ourselves. Or maybe, we should contact BD to see if they have any solutions, as they are the only known company who apply FCS3.2 in industry.
Hi Gabriel, the BD file type can't be changed. If you can contact the guys from the flowcore package, I'll check if we can do something from here in the meanwhile.
Thanks for you reply, I am contacting BD for solutions. I will let you know if I hear any updates from them. By the way, I have another question: how do you determine the scale bar of the images extracted from the machine?
Hi,
If it can help IFC
package has been updated and should hopefully allow FCS files parsing according to recent 3.2 specifications. Still need to test with real-world files, see https://github.com/gitdemont/IFC/issues/4
Hi, If it can help
IFC
package has been updated and should hopefully allow FCS files parsing according to recent 3.2 specifications. Still need to test with real-world files, see gitdemont/IFC#4
Hello Demont,
Thank you for your suggestion! I would test if the package works on my side and let you know asap!
Gabriel
Hi @gabrielpan147 ,
So, did you manage to try things out ?
Best
Hello @gitdemont ,
Sorry I did not work on this project these days, I will find a time to do that!
Best, Gabriel
Thanks for your reply @gabrielpan147 Don't hesitate to comment / submit issue about FCS3.2 support in IFC Best
Latest version of flowcore supports FCS 3.2. However, CytoML, which is required for the line below, does not support FCS 3.2. Any update?
flowjo_to_gatingset(open_flowjo_xml(wsp, sample_names_from="sampleNode"))
Hi alefrol. We depend on the CytoML update as well and hope for the update happening soon. The Flowcore (as you mentioned) has been updated.
Correction to my previous comment: Works now, you just need to install it from their github directly.
For all versions, you must have dependencies installed. library(BiocManager) This should pull all dependencies. BiocManager::install("openCyto")
Then install latest dependencies from github, using devtools. _install.packages("devtools") library(devtools) #load it
install_github("RGLab/flowWorkspace") install_github("RGLab/openCyto") installgithub("RGLab/CytoML")
Hello, I am trying to reproduce the analysis workflow of the paper. I tried to generate a table using R and import it to the Fiji plugin to generate processed images. I just noticed that currently the BD image cytometer generates fcs3.2 format, which is not supported in flowCore module in R. Thus the whole R program can not work properly. Do you have any ideas or suggestions?
Thanks!