Genetics of Human Disease

Study mode:On campus Study type:Full-time Languages: English
Local:$ 17.4 k / Year(s) Foreign:$ 32.7 k / Year(s) Deadline: Jul 28, 2024
16 place StudyQA ranking:2595 Duration:1 year

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The Genetics of Human Disease MSc aims to provide students with an in-depth knowledge of molecular genetics, quantitative and statistical genetics and human disease and how this can be applied to improve healthcare through the development and application of diagnostic tests and therapeutic agents.

The programme provides a thorough grounding in modern approaches to the understanding of the genetics of disease alongside the cutting-edge research methods and techniques used to advance our understanding of development of disease. Core modules provide a broad coverage of the genetics of disease, research skills and social aspects, whilst specialised streams in Inherited Diseases, Pharmacogenetics and Computational Genomics, in which students can qualify, and the research project allow more in-depth analysis in areas of genetics.

Students undertake modules to the value of 180 credits.

The programme consists of four core modules (60 credits) and two specialist modules (30 credits) and a research project culminating in a dissertation (90 credits).

A Postgraduate Diploma consisting of six modules (four core modules in term one and two modules within the selected stream in term two) is offered, full-time nine months.

A Postgraduate Certificate consisting of four core modules in term one (60 credits) is offered, full-time three months.

Core modules

  • Advanced Human Genetics: Research Principles
  • Understanding Bioinformatics Resources and their Applications
  • Core Skills
  • Basic Statistics for Medical Sciences

Specialist modules

In term two you will take specialist modules depending on the specialist stream you select: Inherited Disease (A); Pharmacogenetics (B); Computational Genomics (C). 

  • Applications in Human Genetics (A)
  • Either Genetics of Cardiovascular Disease or Genetics of Neurological Disease (A)
  • Clinical Applications of Pharmacogenetic Tests (B)
  • Anti-Cancer Personalised Medicine or Pharmacogenomics, adverse drug reactions and biomarkers (B)
  • Applications in Human Genetics (C)
  • Statistics for Interpreting Genetic Data (C)

Dissertation/report

Students undertake an original research project investigating topical questions in genetics and genetics of human disease which culminates in a dissertation of 12,000 to 14,000 words and an oral presentation.

Teaching and learning

Students develop their knowledge and understanding of genetics of human diseases through a combination of lectures, seminars, tutorials, presentations and journal clubs. Taught modules are assessed by unseen written examination and/or, written reports, oral presentations and coursework. The research project is assessed by the dissertation and oral presentation. 

Normally, a minimum of an upper-second class Bachelor's degree from a UK university in a relevant discipline such as in biomedical sciences, life sciences or a medical degree (MBBS), or an overseas qualification of an equivalent standard. Applicants with an appropriate professional qualification and relevant work experience may also apply.

Scholarships relevant to this department are displayed below.

Commonwealth Shared Scholarship Scheme (CSSS)

Value:

Full fees, flights, stipend, and other allowances (1 year)

Eligibility:

Overseas students

Criteria:

Based on both academic merit and financial need

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