Saturation genome editing of RAD51C
I completed my master’s degree under the supervision of Dr. David Adams and Dr. Andrew Waters at the Wellcome Sanger Institute. My project investigated variants of uncertain significance (VUS) in RAD51C, a gene associated with breast and ovarian cancer predisposition. I used saturation genome editing (SGE) to systematically characterise all possible single-nucleotide variants in this gene. The findings of this study, now published in Cell, provide a valuable resource to aid in the clinical management of VUS and advance targeted therapies.