National study identifies hereditary causes of childhood cancer – for better follow-up and treatment
Follow-up and treatment of children with cancer is significantly improved when inherited genetic causes are also investigated, according to a new Swedish study. The results of the research study involving some 50 researchers and clinicians from across Sweden have been...
Paediatricians in Sweden propose whole genome sequencing as a routine diagnostic test for all childhood cancer patients
The Swedish Paediatric Association’s Section for Paediatric Haematology and Oncology recommends that whole genome sequencing should be a clinical routine at diagnosis for all childhood cancer patients. “For GMS Childhood Cancer, the statement is a...
Genomic Medicine Sweden awarded SEK 30 million for national and international data sharing for precision medicine
The Swedish Innovation Agency Vinnova has decided to fund the further development and implementation of the National Genomics Platform so that data generated in healthcare can be put to the greatest possible use. For healthcare, research and innovation. “This is...
Using whole-genome sequencing in the diagnostics of acute lymphoblastic leukemia in children
A new Swedish study shows that whole genome sequencing can detect clinically relevant genomic abnormalities in acute lymphoblastic leukemia, ALL, and has great potential to be implemented in the diagnostic setting. The study, conducted by researchers within the GMS...