I am using the gbrowse2 samtools setup to display short read data in terms of coverage plots. Gbrowse is selecting different ranges or limits for the plots (as you see below 8, 20, and 50). I want them all to be the same so they can be compared visually.
How do I set this up so that the plots "know about each other"?
current example of track setup:
[UntreatedReadCoverage] feature = coverage glyph = wiggle_xyplot database = readsUntreated height = 50 fgcolor = black bicolor_pivot = 20 pos_color = blue neg_color = red key = Untreated read coverage category = Coverage label = 0 # Labels on wiggle tracks are redundant.