Thanks again for all of your help in leveraging the great dataset you generated.
I subsetted the whole tonsil cite-seq Seurat object to obtain 2 cite-seq objects (one object for B cells expressing CD38 and one object for B cells not expressing CD38).
I followed the codes you kindly deposited to perform WNN analysis of RNA+ADT for each of these 2 objects, including harmony to integrate by "gem_ID" within each object within each object.
I now hope to merge these 2 B cell objects and cluster them using RNA+ADT.
Would you minding providing some opinion whether I should simply use merge() or what is the recommended workflow?
Hi there,
Thanks again for all of your help in leveraging the great dataset you generated.
I subsetted the whole tonsil cite-seq Seurat object to obtain 2 cite-seq objects (one object for B cells expressing CD38 and one object for B cells not expressing CD38).
I followed the codes you kindly deposited to perform WNN analysis of RNA+ADT for each of these 2 objects, including
harmony
to integrate by "gem_ID" within each object within each object.I now hope to merge these 2 B cell objects and cluster them using RNA+ADT.
Would you minding providing some opinion whether I should simply use
merge()
or what is the recommended workflow?Thank you very much!