Hello,
My laboratory developed an in-house 5'RACE method with custom primers targeting the constant region of the gamma/delta T cells. We submitted RNA to a third party commercial laboratory to benchmark our method against their 5'RACE method. Both our in-house fastq's and the third party's were processed using MiXCR. How legitimate is it to compare clones from the different library prep methods in a longitudinal analysis (more time points were captured in the in-house method than were submitted to the third party)? Thanks!