On 01/21/2016 08:52 AM, Frances Wong wrote:
This is Frances Wong, currently a graduate student at the University of Toronto. I am work on using openCyto to gate my flow Cytometry data but I'm running into some problems. Since I'm doing a screen on 4 separate 96 well plates, I have close to 400 fcs files I would like to gate together but some of the samples have low cell counts and this is causing errors when applying the gating template. Is there an argument to ignore low cell counts? I am currently manually removing these cell counts but I would like a more automated way as I have multiple flowSets I need to analyze.
I was planning on bringing the analysis to the live gate stage and filtering flow low cell counts here but I cannot even apply the singlet gate.
Thank you very much in advanced!