Hi, I'm going through the RNA-seq exercise at http://main.g2.bx.psu.edu/u/jeremy/p/galaxy-rna-seq-analysis-exercise. I'm at step 2 of mapping the reads where I've run tophat and have loaded the output files and the regGene tracks onto a new track browser. When I zoom in (to ~45kbp window), the accepted hits and one of the splice junction tracks from tophat do not show data and instead show a crossed pattern and the browser no longer allows clicking and dragging to move the window. Please advise.
Cheers, Steve
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