Institute for Human Genetics

Inga Nagel


+49 (0) 431 / 500 - 30 625
i.nagel [at]

Research Interest

Inga Nagel

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.