We offer Recommended Track Sets for hg19 and hg38 that display a pre-set browser configuration based on specific areas of interest. These include SNV and CNV interpretation, non-coding variants, exon relevance, problematic regions, and expert panel sets for BRCA1/BRCA2 and Lynch syndrome.
Feel free to contact us if you are interested in attending a workshop, or meeting someone from the team to collaborate, get help, or ask any questions at the meetings. See our Poster Gallery.
Click the images to explore the latest Public Sessions on our main site.