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I think currently we exclude all out of frame CDR3s from any part of the analysis after sequence parsing. It's good to exclude these from analysis since they are non-functional, but it is important to track their clonality, as they are a correlate of clonality signals for functional CDR3s.
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Would we want their clonality to contribute to estimates of clonality for their parent repertoires, or should it be reported separately? And when you say clonality, you mean the overall distribution of clone sizes, or the actual clone sizes for all the out-of-frames?
I think currently we exclude all out of frame CDR3s from any part of the analysis after sequence parsing. It's good to exclude these from analysis since they are non-functional, but it is important to track their clonality, as they are a correlate of clonality signals for functional CDR3s.
The text was updated successfully, but these errors were encountered: