PhD Courses in Denmark

Medical genetics and genomics

Graduate School of Health and Medical Sciences at University of Copenhagen

Enrolment guidelines


This is a specialised course. This means that 80% of the seats are reserved to PhD students enrolled at the Faculty of Health and Medical Sciences at UCPH and 20% of the seats are reserved to PhD students from other Danish Universities/faculties (except CBS).

The course is free of charge for PhD students at Danish universities (except Copenhagen Business School), and for PhD Students from NorDoc member faculties. All other participants must pay the course fee.

Anyone can apply for the course, but if you are not a PhD student at a Danish university, you will be placed on the waiting list until enrollment deadline. This also applies to PhD students from NorDoc member faculties. After the enrollment deadline, available seats will be allocated to applicants on the waiting list.


Learning objectives

A student who has met the objectives of the course will be able to:

1. Understand the human genome structure and explain the effect of variants on protein function

2. Understand and use variant nomenclature

3. Apply ACMG guidelines for variant interpretation and classification (including use of public databases, programs and in silico analysis)

4. Evaluate ethical, legal and clinical considerations in genomic medicine (including data storage, biobank, informed consent, secondary findings and clinical implication of results)


Content

The course will cover a general description of the human genome including the structure of genes and how genetic variants may lead to abnormal RNA and protein. The course includes a brief description of inheritance patterns. The students will be introduced to and work with variant nomenclature, variant filtration and variant interpretation using different tools and software. Various sequencing methods are presented as well as ways to process e.g. genome sequencing data. The course will also cover functional analyses, genetic counselling in practice, genome-wide association studies, the use of biobank data and ethical application for genome research.


Participants

PhD students with a background in medical sciences, biology, biochemistry or similar.


Relevance to graduate programmes

The course is relevant to PhD students from the following graduate programmes at the Graduate School of Health and Medical Sciences, UCPH:

All graduate programmes


Language

English


Form

This is an on-site course based on lectures, case-based group work and expert presentations by invited specialists.


Course director

Elsebet Østergaard
Professor, consultant, PhD
Rigshospitalet
Department of Clinical Genetics
Blegdamsvej 9
2100 Copenhagen
Denmark

And

Department of Clinical Medicine
University of Copenhagen
Blegdamsvej 3
2200 Copenhagen
Mail: Elsebet.oestergaard.01@regionh.dk


Teachers

Zeynep Tumer, professor, Department of Clinical Genetics, Rigshospitalet and UCPH

Thomas van Overeem Hansen, professor, Department of Clinical Genetics, Rigshospitalet and UCPH

Karin Wadt, professor, Department of Clinical Genetics, Rigshospitalet and UCPH

Mette Bertelsen Vardrup, professor, Department of Clinical Genetics, Rigshospitalet and UCPH


Dates

1-3 September 2026


Course location

Rigshospitalet


Registration

Please register before 1 August 2026


Expected frequency

Annually


Seats to PhD students from other Danish universities will be allocated on a first-come, first-served basis and according to the applicable rules.

Applications from other participants will be considered after the last day of enrolment


Note: All applicants are asked to submit invoice details in case of no-show, late cancellation or obligation to pay the course fee (typically non-PhD students). If you are a PhD student, your participation in the course must be in agreement with your principal supervisor.