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Dragging feature boundaries not working as expected for Shine-Dalgarno and CDS #2515
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Can you right-click on the annotation and add the GFF3 for all components in there? |
This is the GFF for the specific example in the screenshot but it's happening across most organisms we've created since the update to 2.6.1 |
@MoffMade I'm not seeing it initially, but I'm sure I don't have the same setup. Can you email me a tarball of the jbrowse directory you are using so I can emulate it. If you could also indicate from which track and how you generated the annotation, that would be helpful. I'm assuming you are running off of the latest. |
Sure thing, let me pull it and I'll send it your way. We're running a fork of 2.6.1 with a couple of docker changes and css modifications. This issue is occurring on features promoted to gene annotations from any of the tracks that have both a Shine-Dalgarno and a Exon/CDS |
Should be noted that the GFF3 I get is fairly similar, with nothing of note incorrect:
However, when I look at the child / parent feature relationship for the exon being edited, the parent is also the same exon . . .
for child feature relationships of feature:
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However, the `bcaf...' does not show up in the GFF3. |
So, the issue is that it goes from gene -> mRNA -> exon -> exon . . . I'm not sure why its creating the second exon or why it was created at that level. I actually removed most of the Shine Dalgarno code because there were some implementation issues, so its surprising it is working at all. I actually thought we were going to wait on this implementation, but its possible that we can work around this, as well. |
So, the issue here is to fix this by:
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@MoffMade This does work for HTMLFeatures:
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You have to drag them up at the same time, and then it works as expected. I think the fix for this is multiple fold.
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We're experiencing some issues dragging the boundaries on gene annotations called from evidence with both a Shine-Dalgarno_sequence and a CDS.
Screenshot of error:
This same error message appears when attempting to "split" a gene with both SD and CDS
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