Hi NGS user,
could anyone give me an advice to detect CNV in targeted exome sequencing?
I'm trying ExomeCNV but I'm not expertize with R and I have some difficult to understand what i have to do.
Thanx a lot
ME
could anyone give me an advice to detect CNV in targeted exome sequencing?
I'm trying ExomeCNV but I'm not expertize with R and I have some difficult to understand what i have to do.
Thanx a lot
ME