Thanks. for your reply before.
But still i don't understand exactly for making coverage.
First of all, I know which tool to use to create the coverage.
But what I still don't know is whether I can define the GRCh38 genome file as eligible territory. In other words, should GRCh38 gtf be converted to bed to bigwig?
Or, read coverage varies from sample to sample, so I have to use different coverage files for each sample.
I'm very thank you for your kindness.
Thanks. for your reply before.
But still i don't understand exactly for making coverage.
First of all, I know which tool to use to create the coverage.
But what I still don't know is whether I can define the GRCh38 genome file as eligible territory. In other words, should GRCh38 gtf be converted to bed to bigwig?
Or, read coverage varies from sample to sample, so I have to use different coverage files for each sample.
I'm very thank you for your kindness.