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Hello. I have a dataset from a Rhapsody analyzer and I'm trying to check for batch effect on the control samples. The first problem I had was to adapt the files because they come in a different format, so I splitted the original file and I created a file with ADT data only and another with RNA only. Then I followed the tutorial for Seurat v4 "Using Seurat with multimodal data" to plot UMAPs. My first question is: Is this the right way to use Rhapsody data in a Seurat pipeline? Thank you for your help. |
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Seurat requires a matrix with features in the rows and cells in the columns to create an assay, if that's what you've generated than that's the correct data format.
Use the |
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Seurat requires a matrix with features in the rows and cells in the columns to create an assay, if that's what you've generated than that's the correct data format.
Use the
group.by
argument inDimPlot()
, and see the documentation forDimPlot()
for more information