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UCT/MRC Human Genetics Research Unit

Director: Prof. Rajkumar S Ramesar
E-mail:
raj.ramesar@uct.ac.za

Prof. RAJ RamesarAn assessment of the current situation in human/medical genome research indicates that it is essential to regroup strategically (and speedily) in order to develop a firm informed base of genomic practitioners, through whom genomic information is sought from our peoples, deciphered, and processed for their betterment.

The way forward is to increase capacity at currently existing academic institutions/departments, units or individual enterprises that practice the various aspects of (Human) Genome analysis.

Prof. RAJ Ramesar heads up the new UCT/MRC Human Genetics Research Unit.

The UCT/MRC Human Genetics Research Unit  benefit from the strong history of excellent research within the host Division of Human Genetics, and  focuses its efforts on the genome research/clinic interface. Building capacity is one of its major outputs.

To date, the Division of Human Genetics has played an important role in:

  • the early diagnosis of inherited disorders, their management and treatment;
  • providing genetic counselling; and
  • conducting research towards offering predictive testing and the possibility of preventing recurrence of respective diseases.

A wealth of data has been built up which is pertinent to disorders in South Africa, reflecting their prevalence, demographic profile in different populations, geographic origins and possible economic burden.

The envisaged expansion of the Unit will be in the areas of:

  • developing a high throughput genetic analysis facility for the purpose of disease-genomic research;
  • training researchers to map and identify genes which are of interest in and to our populations; and
  • understanding the biology of such genetic elements by drawing on the expertise within the Institute for Infectious Diseases and Molecular Medicine on the UCT campus, and other interested bodies in the country.

The core expertise and resident functions in the Unit will ultimately include:

  • genetic study co-ordination which will help with the development and co-ordination of patient, family and population-based studies, and the design of such investigations;
  • assistance with the development of diagnostic criteria and screening for specific research programmes;
  • subject contact and collection of biological material;
  • A high throughput genetic analysis capability to carry out large scale genotyping and sequencing to identify disease-predisposing elements in our populations.
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Last updated:
20 December, 2012
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