Tweet
Interested in identifying rare and common structural variants in an individual? Common structural variants in a population? Disease-causing variants or genes in a cohort?
One winner will receive SMRTbell library construction, sequencing on the Sequel System and bioinformatics analysis from our PacBio Certified Service Provider, the University of Minnesota Genomics Center.
Submit your entry today! Entries due by November 30, 2018
One winner will receive SMRTbell library construction, sequencing on the Sequel System and bioinformatics analysis from our PacBio Certified Service Provider, the University of Minnesota Genomics Center.
Submit your entry today! Entries due by November 30, 2018