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License: GNU General Public License v3.0
a gui tools to filtering genomics variation
License: GNU General Public License v3.0
All filter can be store as a profile
By default, create one table per sample
You may want to use tab to show table separatly
Should be possible to copy cell
database size, etc ...
When you open a second file, the current position in the browser is not kept.
Make a DockWidget which display statistics of variant .
See VEP report
resultView with a button : display sql query
Export filter as Json ..
Same for links !
So.. All inside a settings file
Windows need icon
Check how we can integrated ACMG criteria :
See : https://github.com/WGLab/InterVar
Make user possible to select variant and store them as favorite
Convert Python Sqlite importer to Qt/C++
Samples should appear at first
Would be nice to display somewhere which request was perform...
And maybe a place to run your custom query.
Display intermediate state when not all fields are selected
Should be able to compute bin to make query faster
I would like to filter variant from HPO term.
For instance:
Show me all variants assciated with deafness.
def genesOf("deafness", "heart") = > GJB2 ....
How can we manage this ?
Store hpo into sqlite ? How ?
avoid conflict between version
How to render the result view with unknown data fields ?
CTRL + F = > Show a quick filter
we should be able to import BED , which will be added into filter panel.
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