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I used to use normalID and tumourID for N-T paired samples, and normalID when the sample is by itself. I later realized that the latter was kind of confusing because tumour sample alone can be used to run call-gSNP as well, and that using singleID when the sample is by itself would make more sense. Not urgent though.
The text was updated successfully, but these errors were encountered:
We use sample_id for the overall sample identifier, ex. sample_id = S00-9422, normal_id = S00-9422N_079_114, tumour_id: S00-9422T_027_166. We should clean up the variable names in this pipeline though, there're some inconsistencies across the processes. I'll keep an issue open for this!
I used to use normalID and tumourID for N-T paired samples, and normalID when the sample is by itself. I later realized that the latter was kind of confusing because tumour sample alone can be used to run call-gSNP as well, and that using singleID when the sample is by itself would make more sense. Not urgent though.
The text was updated successfully, but these errors were encountered: