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This repository has been archived by the owner on Oct 15, 2024. It is now read-only.
We should create a DoCM tutorial. This could live on a new page of the DoCM site (e.g. help or getting started).
This tutorial could include things like:
Query using DoCM website to get all variants for a specific disease, all variants for a specific gene, all variants for a region of the genome.
Export results of a query to a VCF file or TSV file
Use the API to perform the same queries. Provide an example script that does this. To lower the bar for a broad variety of users, provide examples written in Perl, Python and Ruby.
The text was updated successfully, but these errors were encountered:
We should create a DoCM tutorial. This could live on a new page of the DoCM site (e.g.
help
orgetting started
).This tutorial could include things like:
The text was updated successfully, but these errors were encountered: