News archive for Genomics Core Facility (GCF)

GCF - Optimizing high throughput protocols and quality control steps (21.11.2019)

Visualization of all variants on chromosome 19

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.

Introduction to Sequencing Workshop (17.03.2017)

Analysis workshop Friday 18 November 2016 (16.11.2016)

Analysis workshop Friday 21.10.2016 (06.10.2016)

Invitation to Next-generation sequencing application seminar (22.08.2016)

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.

Discontinuance of Illumina Human Expression Arrays (Illumina HT-12) (04.05.2016)

New funding to research infrastructure (07.01.2016)

NGC Newsletter (07.01.2016)