Usecase: human genetics researcher #87

Scenario:

• obtain patient id from spreadsheet (first column, bunch of numbers)
• copy paste into epic patient lookup (citrix)
• patient lookup, paste mrn
• chart review tab, labs subtab
• check if any presence of genome diagnostics
• click "genome diagnostics"
• click "external genetic test stored"
• scroll down to where it says "scans on order"
• click on blue link with scan title
• if no genome diagnostic, click "Encounters" tab, "ChartMaxx" button
• click patient name to expand tree
• click "genetic testing"
• click "sent out genetic testing" (may be mulitple)
• press down button until page says "genetic testing report" (or similar)
• extract gene name and mutation (e.g. RS1 gene, c.589 C>T mutation) (may be multiple)
• paste into excel
• then go to clinvar (database of clinical variants)
• google "clinvar" open first link
• paste from excel into search:
• copy and paste interpretation (e.g. "pathogenic")
• paste into excel spreadsheet "categorization"

Scenario:

• parse electrophysiology results from pdf in citrix
• insert into excel