Kornelia Neveling, PhD, is a scientific researcher at the Human Genetics department at the Radboud UMC in Nijmegen, the Netherlands. She earned her degree in Biology at the Heinrich-Heine-University Düsseldorf, Germany. Subsequently, she performed her PhD in Human Genetics at the Julius-Maximilians-University Würzburg, Germany, investigating the molecular causes and consequences of genetic instability syndromes, with a special interest in Fanconi anemia. In 2009, she started as postdoc at the Dept of Human Genetics of the Radboud UMC, where she learned all about NGS. From 2011-2018 she worked at the sequencing facility and since 2018 she joined the Translational Genomics group, both at Genome Diagnostics Nijmegen. Kornelia’s main interest is in the implementation of new technologies into diagnostic routine, with long read sequencing and long read optimal mapping being her current passion.
