Open pieterlukasse opened 1 year ago
Progress update: @forus is going through the docs and the code to get a clear picture of the complete process, the exceptions, edge-cases, etc
@allisonheath @migbro Here is a document with findings of our research and proposal of next steps https://docs.google.com/document/d/1dKwPUKEcmLLVjwRWLwqzMdqBoXCFrVmp_1UDFeKmkec/edit?usp=sharing Please review.
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.
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