Inga Nagel

Institute for Human Genetics

Research Interest

My focus area is the identification of causal constitutional sequence and copy number variants in rare diseases. I am also working on the identification of variants that lead to cancer therapy resistance in hematological malignancies. For both subject areas I am using whole exome sequencing data. My aim is to switch more and more to the analysis of whole genomes to be able to discover pathogenic non-coding variants as well.