Hi.
I'd like to calculate the sequencing coverage from bioscope result.
I try to calculate the sequencing coverage with consensus call file which is from SNPs calling from bioscope. Does it make sense?
Is there the way to calculate the sequencing coverage without SNP calling?
I'd like to calculate the sequencing coverage from bioscope result.
I try to calculate the sequencing coverage with consensus call file which is from SNPs calling from bioscope. Does it make sense?
Is there the way to calculate the sequencing coverage without SNP calling?