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I'm working on my first CITE-Seq project and I had a couple of questions regarding QC.
I've already run WNN analysis and I wanted to calculate the number of cells in each of my clusters expressing each of the surface proteins in my panel. I applied the code described in this comment: #371 (comment). I'm surprised how high the expression levels are in my result (including seeing expression in my isotype controls). And I was wondering if that is to be expected.
I was also wanting to do something analogous to mean fluorescence intensity for my data. Is this something that's possible in Seurat?
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Hello Seurat community,
I'm working on my first CITE-Seq project and I had a couple of questions regarding QC.
I've already run WNN analysis and I wanted to calculate the number of cells in each of my clusters expressing each of the surface proteins in my panel. I applied the code described in this comment: #371 (comment). I'm surprised how high the expression levels are in my result (including seeing expression in my isotype controls). And I was wondering if that is to be expected.
I was also wanting to do something analogous to mean fluorescence intensity for my data. Is this something that's possible in Seurat?
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