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Description
The Bravo variant browser currently shows chromosome locations, alleles, VEP functional annotations, and allele frequencies for 463 million variants observed in 62,784 individuals sequenced in NHLBI's TOPMed program.
https://bravo.sph.umich.edu/freeze5/hg38/about
There is an API here:
https://bravo.sph.umich.edu/freeze5/hg38/help
There doesn't appear to be a swagger JSON, but it's a fairly standard REST-like RPC API, so an OpenAPI description should be straightforward.
Open question: this API (and the browser) requires authorization and authentication (using google for authentication). The setup has clear instructions on how to do this. I assume we want to indicate this in the API registration metadata; how best to do this? Do we want KC6 input on this?