Closed patmagee closed 9 years ago
The PGX_information, can be entered independently of the drug recommendations information. Build two collections, one for the GENES and another one for the specific markers. Basically keep the same layout as is currently used, however have a collection for each. Additionally Build an interface which easily allows for this data to be entered at a later time.
For the user interface, instead of making it an "ADD", make it "Manage" Haplotypes. They should get a list of all the haplotypes that they can modify or delete. (similar to projects), or they should be able to add new phasing information.
This will need to be implemented following the addition of the new pgx drug recommendation information