Entering edit mode
5.2 years ago
avichaireich
▴
10
Hello. I have a SAM file and a referance genome. I'm trying to get a list of all the positions that in the referance it has A and in the alternative is has C, with total depth of at least 20X.
I don't need to do variant call, only get the list of the positions.
I'm a bit lost in this, I'll be happy for help solving it.
Thank you.
Thank you for the quick reply! How can I know what is the depth of each allele?