Our Medical Genomics MSc course will bring you up to speed with the post-genomic era following the game-changing breakthrough that is the sequencing of the human genome. The data now being generated is producing insights at an amazing rate, and personalised medicine is just around the corner. Skilled and talented biologists capable of analysing, processing and innovating are in growing demand by employers. If you're a science graduate who wants to specialise and gain employment in this area, then you can be part of the new golden age in medical genomics with this master's degree.
On this course, you’ll enhance your knowledge of genomic science from a health perspective. As genetic testing becomes part of routine medical evaluations and more geneticists are needed to perform the tests, we can help develop your skills through unique research projects, outstanding teaching and high-quality facilities.
London Met’s superb facilities include a £30 million Science Centre with 280 workstations and specialist laboratories where you can undertake research and refine your hands-on experience. This will greatly enhance your employability upon graduation.
Our research-active staff will be joined guest lecturers from organisations such as Barts Health NHS Trust, Imperial College London, King’s College London, University College London, St George's Hospital and Brunel University. We also maintain a strong collaboration with the prestigious Colombian Institute for the Promotion of Higher Education (ICFES), providing you with the opportunity to sign up to our exciting international work exchange programme.
These connections with prestigious universities mean you’ll have the opportunity to meet and discuss your career options, secure work placements or apply for studentships. When you graduate, you’ll also be eligible to join the Royal Society of Biology, with whom we are registering this course to be accredited in the near future.
The University’s close location to the impressive genome and scientific job market in London means you’ll be well-placed for a career upon graduation. Our Careers and Employability team will help you improve your CV and assist you in your search for employment upon graduation from the Medical Genomics MSc.
You’ll be tested through a wide variety of assessments. You’ll write laboratory reports, give presentations, sit written exams, take part in debates, answer quizzes, experience virtual labs via online learning, make posters and defend your work in presentations.
You will be required to have:
All applicants must be able to demonstrate proficiency in the English language. Applicants who require a Tier 4 student visa may need to provide a Secure English Language Test (SELT) such as Academic IELTS. For more information about English qualifications, please see our English language requirements.
The modules listed below are for the academic year 2018/19 and represent the course modules at this time. Modules and module details (including, but not limited to, location and time) are subject to change over time.
Year 1 modules include:
Introduction to Genetics and Genomics
This module provides information and guidance to faciliatate an indepth understanding and knowledge of the theory and practical applications of molecular biology, genetics and genomics. It explains the underlying mechanisms of molecular biology and enables these ideas to be expanded to the understanding of human health and disease.
This module applies in silico approaches to explore the relationship between genotype and phenotype in the context of human disease and health. It includes an analysis of the influence of genetic variation in human populations to the penetrance of disease phenotype and to responses to environment, lifestyle and therapy. It runs in the Spring semester and is assessed by two pieces of coursework and a presentation. There are no pre-requisites other than satisfaction of general entry requirements.
This module focuses on human diseases with a genetic component, from monogenic disorders to complex, multifactorial diseases. Consideration is also given to hereditary mechanisms not linked to DNA sequence (e.g. genomic imprinting).
This module provides an opportunity for student-lead problem solving applying knowledge acquired to a specific research question.
The module is designed to provide students with an understanding of skills needed for the planning, organisation and practice of research in science. Different analytical approaches to problems will be reviewed together with the need to consider statistics and quality control in the design of projects. Students will consider the impact of appropriate safety, ethical and resourcing implications in the design and operation of a project.
The module focuses on the development and operation of the immune system in both health and disease and explores current research in immunopathology, stem cells and immunotherapy.
The module uses online databases and software to extract, analyse and interpret DNA and protein sequences and to model structures of proteins.
BM7042 Biomedical Diagnostics focuses on current and emerging wet techniques used to analyse disease biomarkers, with an emphasis on genomic markers, for diagnosis in medicine. It runs in the Autumn semester and is assessed by an in-course test and an essay. There are no pre-requisites other than satisfaction of general entry requirements, and it includes a component of laboratory work.
This module focuses on the occurrence of emerging infectious diseases, their origins, evolution and epidemiological features that facilitates their adaptation to, and transmission within, human populations. A range of microbial pathogens will be reviewed and emphasis will be placed on their impact on public health and strategies for disease control. GIS will be covered as an example of an epidemiological tool.
This module provides an opportunity for a formal examination of ethical theories (eg deontology, utilitarianism, care ethics, virtue ethics, etc), and to apply these theories to selected topics in contemporary biomedical science
This module provides an advanced understanding of cancer at the molecular level.
In this course, you will take an introductory module on genetics and Genomics, together with a fascinating module discussing the ethics of science.
With your training in human genetics, many opportunities will be available to you upon graduation. Genomics is important in both public and private domains, and there is increasing demand for new graduates in a growing number of new genome centres and companies in the UK and abroad, such as the Wellcome Trust Sanger Institute in Cambirdge and Medgenome in India. Genomics is also a key area for the NHS, with governmental initiatives such as the 100,000 Genomes Project.
As genetics becomes a recognised part of all biological sciences, there will be an increasing demand for individuals with expertise in this field.
Please note, in addition to the tuition fee there may be additional costs for things like equipment, materials, printing, textbooks, trips or professional body fees.
Additionally, there may be other activities that are not formally part of your course and not required to complete your course, but which you may find helpful (for example, optional field trips). The costs of these are additional to your tuition fee and the fees set out above and will be notified when the activity is being arranged.
Use the apply button to begin your application.
You are advised to apply as early as possible as applications will only be considered if there are places available on the course.
Please select when you would like to start: