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Lack of an existing "somatic event ID" to tie DNA and RNA data together...eventually methylation data, etc. This actually surfaced today as a primary complaint from another project, as when they do molecular subtyping, it's causing conflict not being able to resolve multiple samples per patient.
Priority:
High
Desired solution:
Unified and clear interface for getting a unique "somatic event id" for any given sample id
Preferred or recommended technical approach:
DoD:
Questions
How does the current mapping process look like? We need to map the different scenarios.
Ideas
Maybe we can come up with a well-defined central "somatic event id" process that is configurable per study?
The text was updated successfully, but these errors were encountered:
Lack of an existing "somatic event ID" to tie DNA and RNA data together...eventually methylation data, etc. This actually surfaced today as a primary complaint from another project, as when they do molecular subtyping, it's causing conflict not being able to resolve multiple samples per patient.
Priority:
Desired solution:
Preferred or recommended technical approach:
DoD:
Questions
Ideas
The text was updated successfully, but these errors were encountered: