Charlotte Gustafsson

The paper introduces T-RHEX-RNAseq, a method for generating stranded RNAseq libraries from very low numbers of lysed cells without RNA purification steps.

This study uses linked-read whole-genome sequencing to detect structural variants and copy number variations in multiple myeloma, identifying both common and private variants that affect gene regulation and molecular classification.

This paper introduces HT-ChIPmentation, a method that enables rapid ChIP-seq data generation from very low cell numbers by eliminating DNA purification and reducing reverse-crosslinking time.