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There are some basic things that we can reiterate in this step:
- What data should look like (usually this is not an issue because processed data is pretty standard format, but doesn't hurt to provide example)
- Enough clinical data
- The CELLxGENE template that we use
- Types of issues encountered in the past
- General flow of review and implementation, e.g. Team Data Contributor -> Sage DCC staff -> MSK DCC -> CELLxGENE engineers
How much are we able to support an alternative/branch of the workflow to Broad portal? (need to discuss internally).
inodb
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