Open SonjaR-UniMan opened 8 months ago
First step: simple python script fulfilling in- and output criteria. Second step: create an endpoint to display in our own API to use this module on its own. Input: HGVS genomic variant description, output a json array containing all the MANE and MANE Select Plus data for the variant.
Third step: json output translated to Python dict to better rework, sort, filter data according to needs.
Fourth step: Module automated testing added to tests folder.
Fourth step: Module automated testing added to tests folder.
looking great. Will have a look at it as reference for module 4
First step: simple python script fulfilling in- and output criteria. Second step: create an endpoint to display in our own API to use this module on its own. Input: HGVS genomic variant description, output a json array containing all the MANE and MANE Select Plus data for the variant.
yup a working API without a code that pull the correct data will cause problem for the user
Use HGVS genomic variant description as input and get MANE and MANE+Clinical variant description as output from VariantValidator using the requests module.