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I used the R package supercell to merge the single cells with high transcriptomic similarity, and generate metacell, and use the metacell data to build seurat object.
For metacell's seurat objects, can I use the standard process of R package seurat to process and analyze them?
The text was updated successfully, but these errors were encountered:
I used the R package supercell to merge the single cells with high transcriptomic similarity, and generate metacell, and use the metacell data to build seurat object.
For metacell's seurat objects, can I use the standard process of R package seurat to process and analyze them?
The text was updated successfully, but these errors were encountered: