News archive for Genomics Core Facility (GCF)
RareVariantVis: a new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data. (07.03.2018)
A bioinformatic tool made by Tomasz Stokowy at the UiB Genomic Core Facility.
Regarding our new Illumina HiSeq4000 sequencing system at the Genomics Core Facility we are happy to invite you to a NGS application seminar on Thursday September 8th, the seminar is hosted in a collaboration with Illumina.