Hey, I am new to BCR sequencing analysis and nextflow in general, but fairly experienced in other bioinformatic fields. I work in a core facility, so I rarely get to go in depth of the projects I am assigned. I just finished running a BCR bulk on heavychain sequencing data. At the moment I have these two questions on my mind: 1. How do I present the results to the PI? Do I just share the /results folder which contains the /clonal_analysis /fastp /fastqc ... ? And is it likely that the PI (who we assume has no computational experience) understands how to interpert the files in the /results folder? 2. Is there more to BCR sequencing analysis? Can I generate more results from one of the output files? Extra: I also recieved bulk lightchain sequencing data and BCR single cell data (which I am going to push through airrflow asap), so in addition to my question 2, can these extra sequencing results be combined to create more meaningful results?