-
Notifications
You must be signed in to change notification settings - Fork 1
Open
Description
Hi!
I’m currently using a real scRNA-seq reference dataset as input to simuRNAseq, and I noticed that the gene names (rownames) in the simulated counts matrix (dat$counts) do not match the gene names in my original reference panel (input counts matrix).
Would it be possible to clarify:
- Why gene names are randomized or replaced in the output?
- Whether there is a way to retain the original gene identifiers from the input panel?
This would be very helpful for realistic benchmarking scenarios where preserving gene identity is important.
Thank you!
Metadata
Metadata
Assignees
Labels
No labels