麻豆原创

Course description

This course brings together the biggest recent advances in biology so you can understand human disease in detail, at the most fundamental level. It covers the cellular, molecular and genetic factors behind a wide range of illnesses, and how new technologies are revolutionising scientific discovery, diagnosis and treatment.

You will study diseases that are caused by a single gene defect, and the more complex molecular mechanisms that lead to cancer, as well as chronic diseases with overlapping causes that primarily affect ageing populations. You will also learn about the role of the immune system and, in the laboratory, you will examine models of the immune system in healthy and diseased states.

There is training on RNA and DNA sequencing, mass spectrometry techniques, and how these are used to process huge volumes of bioinformatic data to better understand disease. In computational laboratories, you will learn how to map genetic sequences, design PCR reactions that allow you to study your data in more detail, and identify genetic variations in a patient, for example. There is also an optional introduction to the programming language R, which can be used to analyse and present complex data sets.

The course also explains how studying disease at a molecular level can lead to new treatment options for patients. You can learn about a variety of biologic therapies developed in the biotechnology and pharmaceutical industries, and how potential new drugs are identified, designed and tested.

You will also complete a research skills training programme and, after all other teaching has been completed, you will spend 20 weeks working full-time on your own research project. Working as part of a team of professional scientists, you will have the opportunity to test a hypothesis, design experiments, analyse your results and present your findings.