Entering edit mode
22 months ago
Sara
▴
270
I have 6 scRNAseq
samples from 2 conditions including 3 treatments and 3 controls (from the same run and same experiment) and we have used 10X genomics
. I have the samples in separate files in h5
format and trying to find a way to merge them all in a single file but so far did not find a way to do it correctly. my final goal is to perform gene expression analysis and marker detection.
In R, you can load in the files individually into Seurat with the Read10x_h5 function into a list, and then merge them all with the merge function there.