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
I would like to use CaSpER to a 10x scRNA-seq tumor dataset, and I know the group of normal cells. The bam file contains reads from all the cells ( it has both the normal and the cancer cells). Do I need to filter out the reads from the normal cells from the bam file before using BAFExtract? Can you please suggest the best practice in this case for identifying regions with copy number variation using CaSpER?
The text was updated successfully, but these errors were encountered:
Hello Dr. Akdes,
I would like to use CaSpER to a 10x scRNA-seq tumor dataset, and I know the group of normal cells. The bam file contains reads from all the cells ( it has both the normal and the cancer cells). Do I need to filter out the reads from the normal cells from the bam file before using BAFExtract? Can you please suggest the best practice in this case for identifying regions with copy number variation using CaSpER?
The text was updated successfully, but these errors were encountered: