How can I use HiFi bioinformatics to uncover germline variation?

This video walks you through HiFi sequencing bioinformatics for uncovering germline variation. The talk covers how HiFi reads can provide a better view of genome completeness, an overview of SMRT Link and the GitHub tools that are available for variant calling, information about the PacBio Whole Genome Sequencing variant pipeline, and finally, we take a look at the PacBio compatible partners ecosystem and some helpful additional resources to get you started.