Entering edit mode
6.5 years ago
Tania
▴
180
Hi Every one
I am checking an interesting variant in a duplicate gene. I am checking mappability of the region, I get the Duke Unique_35 mappability from the UCSC genome browser. I took a window size greater than my read length and found the mappability is 1. Does this make sense given the gene is a duplicate? I thought if the gene is duplicate then it will have lower mappability? And is the window size reasonable? Am I missing anything here?
Thanks
. I took a window size greater than my read length and found the mappability is 1.
how did you get that number ? cmd line ?
From IGV, I got the read length, say 150 and my variant is in the middle for example. then I checked the position of this gene by considering around 200 bases around my variant (I mean including the read length) in this window. I looked for Duke Unique_35 mappability in the UCSC. No command line.
Not sure if I explain it well.