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Quick question: I noticed each of the results are per sample. It makes sense as that’s how they were obtained, but I’m wondering if it would be easier for reusers of the data if we share the results as a patient level attribute as well. Basically we would make some informed decision on how to assign a patient’s ancestry given the results from one or more samples
Yea, it is a good question. Averaging would be fine with me if they are pretty consistent across samples within a patient.
The text was updated successfully, but these errors were encountered:
htan_singlecell_ancestry.zip
Notes
We can average the calls per patient:
The text was updated successfully, but these errors were encountered: