Clinical and Technical Working Groups

The Working Group for Clinical use of Whole Genome Sequencing has been established by the Danish National Genome Center in collaboration with the regions and the Organization of Danish Medical Societies (LVS) to ensure a coordinated effort for the development of whole genome sequencing for clinical use in the healthcare system. The working group for clinical use of whole genome sequencing advises the Steering Group on the selection of patient groups to be offered whole genome sequencing via the Danish National Genome Center.

Mandate and Members (In Danish)

The National Specialist Network for Rare Diseases has been established by the Danish National Genome Center in collaboration with the regions, the Organization of Danish Medical Societies (LVS) and the Danish Society of Clinical Academics (DSKA).

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on endocrinological patients (e.g. patients with diabetes, goitre and metabolic diseases, osteoporosis, etc.) to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on hereditary haematological disease, incl. children and young people with unresolved cytopenia (patients with blood diseases, e.g. leukaemia) to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on children and young people with cancer (up to 18 years) and hereditary cancer to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Cancer in Adults (18-30 Years) and Hereditary Cancer in Adults to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Primary Immune Deficiency Diseases to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Hereditary Heart Diseases to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Haematological Cancer to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Psychiatry Children and Young People under 18 Years of Age to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Kidney Faillure to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Fetal Medicine to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

The National Specialist Network must provide health professional advice on Neurogenetic Patients to the Danish National Genome Center for use in the national introduction of whole genome sequencing.

Mandate and Members (In Danish)

Mandate and Members (In Danish)

Mandate and Members (In Danish)

Mandate and Members (In Danish)