Open CNicholasMDA opened 6 years ago
Additional information/feedback on my issue of Oct 2: I have detected that this bug also affects regrouping (renaming) of the Sample IDs. I began with an RData results file that contained 118 samples. After regrouping (modifying) the sample names, I only had 99 samples loaded in the GUI. There was no rhyme or reason to indicate why a particular subset of samples were dropped (no special characters, etc).
Any help or suggestions you have are greatly appreciated. Is it possible that I have a problem with a supporting package that is installed?
thank you, Courtney
Hi Courtney, I noticed the same thing when I used it and it is an interesting yet weird bug. not sure we will get a response on it.
This is still an issue. Do not rename your markers.
Dear Users,
Thank you very much for your support and feedback. We will fix this bug by this week and update you.
Very sorry for slow reply. I will improve my communication on github forum. And many thanks to Sam who highlighted this issue to me.
Best, Jinmiao
Dear Users,
We have fixed this bug and updated on cytofkit2 at https://github.com/JinmiaoChenLab/cytofkit2
Please download and test it.
Thank you.
Best, Jinmiao
Hi Dr Chen and team, Thank you. This is a great effort. We appreciate it. I do have one question - during this latest install (instructions in the abovementioned link for cytofkit2) I find that the program cannot find a package called cytofkit2. Which line of the installation instructions pertains to downloading and installing cytofkit2?
with thanks, Courtney
Hi Courtney, The installation procedure is at https://github.com/JinmiaoChenLab/cytofkit2 in the scetion "Install this development version". Briefly:
if(!require(devtools)){
install.packages("devtools") # If not already installed
}
devtools::install_github("JinmiaoChenLab/cytofkit2")
To use it:
library("cytofkit2")
cytofkit_shiny_dashboard()
Hello Dr Chen and colleagues, I am enjoying the use of your cyTOFKIT program. Thank you for working so hard to make it user-friendly while executing various important clustering algorithms.
However, today I have encountered a problem and am not sure if it is user error or software error.
When I run the clustering algorithm and open the results in the shinyAPP viewer, I frequently like to re-name my protein markers and re-group my samples to rename them. However, I have noticed that after updating the marker names, the distribution of markers (CD3, for example) changes in the Marker Expression Level Plot. In addition, the expression pattern in the newly-assigned CD4 plot looks disturbingly similar to the “old” CD8a plot. This occurs regardless of whether I export a new RData file after updating the marker names.
Am I using a setting incorrectly, or is there a known software issue? (For now, I will be happy with not changing the marker names…)
image of CD3, CD4, and CD8a prior to marker re-naming:
image of CD3, CD4, and CD8a after marker re-naming:
Any suggestions you can offer are greatly appreciated.