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When I pass `channel_alias` argument in `parseWorkspace`, I expect that it will update the channel names in compensation matrices, transformations, and gates; however, it's only changing the channel n…
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Hi Jon,
First, profuse thanks for writing RScattnlay! I'm an R guy, and have written an R wrapper for bhmie, but now need to do multi-layer particles, and your code seems to be the class act.
I…
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Bonjour @NataliyaSokolovska , @julibinho
J'ai une question sur les résultats des fichiers CyTOF,
Comment peut-on trouver l'existence du cytomegalovirus antibodies dans chaque sample?
je collec…
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Hi,
thank you for this package, it works quite nicely and is much faster than Phenograph!
I am working with 20 million cells from a flow cytometry analysis. When I used a comparatively low "k" (…
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Hi,
In step five of the work example, you set the lower bound to 0. Now I want zeros to be considered so I changed 0 to -0.01. However, it turned out that the code chunk in step seven keeps running…
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Hi there,
I am trying to use your package on flow cytometry data using an examplary dataset of ~30.000 cells and 5 dimensions with a pre-set start_id. The fluorescence data is wrapped into counts a…
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Hi,
Thank for making nQuire. I've installed and run the program successfully (and easily, great job!). I'm testing nQuire on a mixed bacterial sample of somewhat known composition. In this case, th…
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I just tried to assembly the tetraploid with MaSuRca 3.2.7, but the file "PLOIDY.txt" shows "1", how can I fix that?
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Dear authors
thanks for the useful package and I have the following error reporting:
```
> Embase
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Is there any way to make the color corresponding with 0 density white and have the color approach red as the density increases?