@@ -142,7 +142,9 @@ e-value, number of reads) about each clone.
In addition, depending on what the user launched on this clone, we may also
find detailed informations retrieved from IMGT or from CloneDB.
#### Detailed information from CloneDB (experimental feature)
#### Detailed information from CloneDB
(experimental feature)
If you are connected to a patient/experiment database where CloneDB is enabled,
and if CloneDB was launched on the selected clone,
you can see here occurrences of this clone in CloneDB
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@@ -207,9 +209,32 @@ The sequence panel displays nucleotide sequences from selected clones.
- See "[What is the sequence displayed for each clone ?](#what-is-the-sequence-displayed-for-each-clone)" below
- Sequences can be aligned together (“align” button), identifying substitutions, insertions and deletions. Silent mutations are identified, as soon as a CDR3 is detected, and represented with a double border in blue.
- You can remove sequences from the aligner (and the selection) by clicking on the “X” at the left.
- You can further analyze the sequences with IMGT/V-QUEST, IgBlast or Blast. This opens another window/tab.
- You can unselect all sequences by clicking on the background of the grid.
## Further sequence analysis with external software
The sequence panel displays buttons to further analyze the selected sequences