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Let’s shape the future - University of Antwerp
The University of Antwerp is a dynamic, forward-thinking, European university. We offer an innovative academic education to more than 20000 students, conduct pioneering scientific research and play an important service-providing role in society. We are one of the largest, most international and most innovative employers in the region. With more than 6000 employees from 100 different countries, we are helping to build tomorrow's world every day. Through top scientific research, we push back boundaries and set a course for the future – a future that you can help to shape.
For a whole genome sequencing project at the Center for Medical Genetics (CMG) in the Faculty of Medicine and Health Sciences of the University of Antwerp is looking for a full-time (100%) doctoral scholarship holder in the field of “From Genome to Diagnosis: Clinical Application and Translation of Whole Genome Sequencing in Rare Disease Diagnostics”.
Help Shape the Future of Whole Genome Sequencing Diagnostics
Over the past decade, next generation sequencing has undergone a remarkable evolution. What began with targeted gene panel testing has progressed to exome sequencing and, ultimately, whole genome sequencing. As sequencing technologies become faster, more accurate and more affordable, both short-read and long-read whole genome sequencing (sr/lrWGS) are now moving within reach of routine clinical diagnostics. These technologies open up new possibilities for identifying the genetic causes of rare diseases, including in patients for whom conventional diagnostic approaches have not provided an answer. At the same time, long-read WGS introduces new challenges, particularly in the areas of bioinformatics, data analysis and clinical interpretation.
As part of this PhD project, you will have the opportunity to contribute to the clinical application and translation of whole genome sequencing in the diagnosis of rare diseases. You will work with sr/lrWGS data and help develop innovative analytical approaches that will take genetic diagnostics to the next level. Your research will focus on, among other topics:
In doing so, you will contribute to a future in which more patients with rare diseases receive a faster and more accurate diagnosis.
The project will be executed at the Antwerp CMG, embedded within the University of Antwerp and the Antwerp University Hospital. It has built up substantial know-how and infrastructure in the field of clinical, molecular and pathophysiological investigation of hereditary diseases, including heart and large vessel diseases, hearing loss, cancer, bone diseases and intellectual disability. Within this environment, the research teams of Prof. Dr. Loeys and Prof. Dr. Meuwissen spearhead the projects focused on cardiovascular and neurodevelopmental disorders. The project will be co‑supervised by Dr Dale Annear and Prof Josephina Meester, which both have a strong background in bio-informatic analysis of genome datasets.
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The University of Antwerp received the European Commission’s HR Excellence in Research Award for its HR policy. We are a sustainable, family-friendly organisation which invests in its employees’ growth. We encourage diversity and attach great importance to an inclusive working environment and equal opportunities, regardless of gender identity, disability, race, ethnicity, religion or belief, sexual orientation or age. We encourage people from diverse backgrounds and with diverse characteristics to apply.
The University of Antwerp is characterised by its high standards in education, internationally competitive research and entrepreneurial approach.
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