EU Udbud Interpretation tool for somatic variants v2

Description

The core mission of the NGC is to establish and operate a state-of-the-art and secure national infrastructure for personalised medicine in cooperation with the Regions and universities. NGC routinely performs Whole Genome Sequencing (WGS) and subsequent bioinformatics analysis of samples from the regional healthcare system. Several patient groups with various diseases have already been enrolled, including cancer patients. For this, NGC needs an interpretation tool for analysing somatic variants. NGC sequences WGS samples at NGC’s sequencing facilities, followed by processing by bioinformatics pipelines developed in-house. After quality control, processed samples are relayed to clinical academics in the regional healthcare system for interpretation and treatment decision(s).