You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
This is a really cool tool that combines two of my favourite scRNA methods!
I was wondering if you could provide any advice regarding the use of unmatched scRNA/snRNA seq as the reference for deconvolution in cases where only visium data is available for the sample and the source of scRNAseq for deconvolution would be a different sample of the same tissue/cancer type?
Of course it is less ideal, but I was wondering if you have been able to try this approach at all?
Thanks,
Ido
The text was updated successfully, but these errors were encountered:
Hi PrismSpot developers,
This is a really cool tool that combines two of my favourite scRNA methods!
I was wondering if you could provide any advice regarding the use of unmatched scRNA/snRNA seq as the reference for deconvolution in cases where only visium data is available for the sample and the source of scRNAseq for deconvolution would be a different sample of the same tissue/cancer type?
Of course it is less ideal, but I was wondering if you have been able to try this approach at all?
Thanks,
Ido
The text was updated successfully, but these errors were encountered: