See II.2.4

The Centre for Human Genetics wants to purchase a new software for the interpretation of next-generation sequencing data. This platform is used for viewing, filtering, analyzing and reporting genetic variants. The raw data comes from the Genomics Core and will be loaded into the software. Based on this software, a clinical and biochemical interpretation can be performed for classifying genetic variant as benign or pathogenic. This interpreted data can then be sent via LIS to the requesting doctor in the form of a clinical report.