Entering edit mode
9 months ago
Santhi
•
0
I have a few sequences that are not annotated in the reference genome. Using BLAST and STAR I was able to get the coordinates of all those sequences. Using IGV, I could visualize that my transcriptomic data has reads mapped to these coordinates. How can I quantify them?? Do I need to customize my gtf file? If yes, how can I do that?