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Hello,
I had a question regarding the MiXCR's defaut library reference sequences. I noticed there were some differences in terms of list of alleles for specific v genes and what v genes were included in the reference sequences. Could you elaborate little more on how the default library was built?
Also, if i would want to compare the scTCR output from cell ranger with bulk TCR output from MiXCR to do clonotype expansion tracking over time, how would you recommend synchronizing the reference sequences?
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