populationgenomics / automated-interpretation-pipeline

Rare Disease variant prioritisation MVP
MIT License
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move metadata registration into a separate process #278

Closed MattWellie closed 1 year ago

MattWellie commented 1 year ago

Motivation

Addition of the mandatory metamist file registration was dumb, and will break the MSFT implementation.

Given that I'm planning to ditch work on this codebase for a while I'm rolling a few currently open issues into this single change.

Fixes

Proposed Changes

Checklist

MattWellie commented 1 year ago

https://test-web.populationgenomics.org.au/ohmr3-mendelian/reanalysis/chr2_denovo_test/summary_output.html was generated using this form (limited to just chr2 variants in the latest ohmr3-mendelian joint call)

Note - there are two samples reaching the report, from the same family, so there's a bunch of similar identifiers but I've checked that it's accurate

jeremiahwander commented 1 year ago

Thanks for the refactor, this is going to be really helpful on our end!