Hi,
I am wondering if I could use the same sequencing library for CNV and SNP calling? In general, how much is the library size for CNV calling? Most of the researches emphasize their sequencing depth and I am not sure if the fragment size is the longer the better?
Thank you in advance.
Jie
I am wondering if I could use the same sequencing library for CNV and SNP calling? In general, how much is the library size for CNV calling? Most of the researches emphasize their sequencing depth and I am not sure if the fragment size is the longer the better?
Thank you in advance.
Jie