Hi,
I was looking at your paper and I was wondering if your method works for multi-patient integration instead of multi-sample integration. i.e. if you have multiple slices from several different patient would I be able to get a batch corrected object that I can compare with RPCA in seurat e.g. (i.e. use single cell approaches for spatial data integration).
Hi,
I was looking at your paper and I was wondering if your method works for multi-patient integration instead of multi-sample integration. i.e. if you have multiple slices from several different patient would I be able to get a batch corrected object that I can compare with RPCA in seurat e.g. (i.e. use single cell approaches for spatial data integration).