Hello Christian,
I found this FAQ on the IGV web site. They may be the best resource for
resolving display issues if they continue. Comparing results between IGV
and Galaxy's visualization tool Trackster can help you to determine the
root cause of the problem.
Hi people, I have a litle problem with Bowtie alignments. I am tryin to align
sRNA Illumina dataset to hairpin mirbase. The problem is that after the steps
(detailed below) I only obtain reads of 15-18nt, and I know that I have a lot
of microRNAs (20-22nt) in my data. Beside the size problem,
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