Research projects overview
- DETECT study: Detection of structural genomic variants causing hereditary cancer (Norwegian Cancer Society project #281610): Millionsatsing på dristig kreftforskning (kreftforeningen.no)
- Norwegian Sequencing Centre (www.sequencing.uio.no)
- Long-read DNA sequencing with oxford Nanopore technology (Oxford Nanopore Technologies)
- Structural Variant Detection with Bionano optical genome mapping (Bionano Genomics | Structural Variation Detection with Optical Genome Mapping)
- Functional assay of FBN1 secretion (together with Benedicte Paus, OUH - Group members (ous-research.no)