Hello Fabricia,
You are probably running the tool like this, correct? This lumps the
upstream flank and downstream flank ends to create one interval:
"Region:" Whole feature
"Location of the flanking region/s:" Both
"Offset" 0
"Length of the flanking region(s):" 7000
Instead, run the tool in
Hi Jen,
Thanks a lot for your reply. But I think you misuderstood my question. I will
reformulate it given examples.
I have initially (because I am doing just preliminary analysis) 70 blat hits
corresponding to different coordinates in the pig genome.
What I would like to have is the flanking r
2 matches
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