You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
I have found many display errors like this. if the reads can alignment match, it will be orange or bisque bgcolor. But when I zoom in to 200bp enough observed base sequence, I found many base sequence display errors, it was a error arrangement. But it was the reverse compliment sequence of the real sequence.
the detail dispaly is like this: http://7xubqr.com1.z0.glb.clouddn.com/gbrwose_dispaly_errors.png
I have found many display errors like this. if the reads can alignment match, it will be orange or bisque bgcolor. But when I zoom in to 200bp enough observed base sequence, I found many base sequence display errors, it was a error arrangement. But it was the reverse compliment sequence of the real sequence.
the detail dispaly is like this:
http://7xubqr.com1.z0.glb.clouddn.com/gbrwose_dispaly_errors.png
my GBrowse is here: http://211.69.128.148/cgi-bin/gb2/gbrowse/soybean/
an example location: NC_016088.2:14,195,894..14,196,026
The text was updated successfully, but these errors were encountered: