populationgenomics / automated-interpretation-pipeline

Rare Disease variant prioritisation MVP
MIT License
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161 base jinja template for report #169

Closed daniaki closed 1 year ago

daniaki commented 1 year ago

Proposed Changes

Checklist

MattWellie commented 1 year ago

Couple of things to investigate - Variant IDs aren't rendering as hyperlinks CSQ field is first-character only

(I'll check it out, just keeping note)

MattWellie commented 1 year ago

contains changes to 30+ files because I'm a sucker for a messy rebase. In addition to @daniaki 's templating changes, I've made a few additions -

This could be extended in a couple of ways, but I think it's a good stopping point for now. Next move is to get this whole application bundled into a docker image, so I'd like this change in prior to that.

An example of the report this generates is here: https://test-web.populationgenomics.org.au/acute-care/reanalysis/2022-12-14/summary_output.html

Please note that this was part of some simulated retrospective work, so the 'forbidden genes' list would never be this long in regular usage