for datasets out of the snRNA-Seq+ATAC-Seq (multiome data) is still fine to use these parameters for the metadata.tab file:
name technology targetnumcells
XX013 10xv3 10000
or should the technology field be updated with something else?
I see that from 8K cells, only about 1,5K are in output (where the same sample sequenced on normal 10x chemistry v3 I get about 5K cells from 8,5K that I start with.
Hi,
for datasets out of the snRNA-Seq+ATAC-Seq (multiome data) is still fine to use these parameters for the metadata.tab file:
or should the technology field be updated with something else?
I see that from 8K cells, only about 1,5K are in output (where the same sample sequenced on normal 10x chemistry v3 I get about 5K cells from 8,5K that I start with.
Thanks, Alessandro.