Short course

Genomics of Common and Rare Inherited Diseases

This five-day specialised microcredential will provide you with a comprehensive foundation in rare inherited diseases helping you understand the patient and family perspective and look at the variety of approaches used to identify genes responsible for common and rare diseases.  

Start date
Monday 3rd February
Duration
5 days
Mode
Face-to-face
Cost
Home - £1000
Level
Postgraduate Microcredential
Credit
15 credits

Overview

The aim of this microcredential is to provide an introduction to the clinical presentation and manifestations of common and rare inherited diseases. The microcredential will also consider the patient and family perspective with respect to the role and impact of genomics, and provide an overview of the approaches used to identify the underlying genes involved.

This microcredential will initially explore the clinical presentation, diagnosis, management and treatment of a range of common and rare inherited diseases. The principles and practice of medical genetics and genomics, and the management and treatment of patients and their families will be discussed. In addition, the role of genomics in a care pathway will be examined including the patient and family perspective.

This microcredential will explore the traditional and current approaches used to identify genes responsible for common and rare inherited diseases, focusing on the latter. Building on knowledge gained in the Omics Techniques and Technologies microcredential, students will further explore the analytical challenges in genomics as applied to rare inherited diseases.

This microcredential will also describe the Genomics England 100,000 Genomes project and data infrastructure and through practical examples highlight which how patients with unmet diagnostic need will benefit from exome or whole genome sequencing.

Content

  • Landscape of common and rare inherited diseases, including: definition; prevalence; age of onset; number of rare diseases with identified associated genes; and number of common diseases with an associated genetic cause.
  • Clinical presentation and course of a range of rare inherited and common diseases.
  • Principles and practise of medical genetics; risk stratification and management of patients and their families, including cascade testing and clinical surveillance.
  • Approaches and techniques used to identify genes responsible for common and rare inherited diseases (for example, candidate gene, positional mapping, genome wide association studies, exome/whole-genome sequencing, use of population data sets, and network biology).
  • Basic statistics to aid interpretation of Genome Wide Associated Studies (GWAS) and analysis of populations.
  • The NHS Genomic Medicine Service and National Genomic Research Library, and their data infrastructures.
  • Selection of tractable cases with unmet diagnostic need, suitable for whole genome analysis.
  • Analytical challenges in genomics as applied to rare inherited diseases including: the potential of electronic health records to enrich patient data; the importance of phenotyping, and use of databases such as ClinVar, and an understanding of the Human Phenotype Ontology; use of large population datasets; and sharing information, for example, Human Variome Project.
  • Clinical use of genomic data, including: awareness of standardised nomenclature used when reporting the results; diagnostic yield; multidisciplinary care; data storage; and patient confidentiality.

Attendance required

On campus teaching will take place on 5 days: Monday 3rd - Wednesday 5th February and Thursday 13th - Friday 14th February 2025.

Leads

Professor Tim Barrett (Professor of Paediatrics and Child Health, University of Birmingham and Honorary Consultant Paediatric Endocrinology and Diabetes, Birmingham Children’s Hospital).
Dr Richard Tuxworth (Senior Lecturer, Department of Cancer and Genomic Sciences).

Prerequisites

You should have a good honours degree in a life sciences subject, although we will consider applicants with alternative qualifications and professional experience within the health service or other relevant background. You should either take Fundamentals in Human Genetics and Genomics and Omics Techniques and Technologies and their Application to Genomic Medicine first, or be able to show you have equivalent knowledge and understanding to enable you to benefit from this module. 

Please contact the Programme Administrator for further information at genomics@contacts.bham.ac.uk

Please note this microcredential is available for home applicants only.

Why choose a Postgraduate Microcredential short course?

  • Usually taken from exisiting modules within a Masters, they can be used as standalone credentials with some also counting as academic credits at postgraduate level
  • Add a postgraduate level qualification to your CV
  • Develop the specialist skills you need for your career goals
  • Alumni status with the University of Birmingham
  • Learners will have the same access to our student support and campus facilities as our students on full degree programmes.

Apply for the Microcredential