Hello, I was recently informed that there are some individuals that overlap between the RNA-seq bulk samples for the libd_scz and CMC_HBCC cohorts, although the processing of the RNA and sequencing was done separately. I am having a hard time being able to figure how to match individual sources between these cohorts. Is it possible to match individuals that were used in both cohorts? Or are they labeled separately by each cohort and therefore cannot be matched between the cohorts? Thank you for your help.