Comments (1)
I think we are happy with this new design.
I know we were still discussing how to get VariantSets/Genes/etc. in there. I think we go with the extra breadcrumb button in the Analyze tab, where we'll show the list of whatevers, and then when a person make a selection, jump back to showing Variants with the relevant filter applied.
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Related Issues (20)
- Contig assembly on bootstrap data fails HOT 1
- On variant csv export, what to do about LONG REF/ALT alleles?
- In pre-contig run cleanup, delete old error reports? HOT 1
- JBrowse warning when re-running contig pipeline HOT 2
- Contig calling shows QUEUED_TO_ASSEMBLE even though really ASSEMBLING, sometimes.
- Velvetg runs out of memory during graph building
- Make queries be case insensitive
- Jbrowse tracks for deleted alignments get left behind
- OptMAGE support doesn't work for multi-bp SNVs
- OptMAGE only works with MG1655
- Genbank exported from latest version of Geneious appears to cause error
- filter key Gene non-functional
- jbrowse contig fail
- How is extremely high-coverage defined? HOT 1
- Generate New Reference Genome: ERROR: More than one record found in handle HOT 5
- Files uploaded through browser remain in /tmp after completion
- Problem uploading samples HOT 36
- Is there any interactive/guided in-depth tutorial available? HOT 1
- Will you be updating to Python 3? HOT 1
- ALIGNMENT PIPELINE ERROR HOT 2
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