Pharmacogenomics of rare and inherited diseases

Pharmacogenomics of rare and inherited diseases

This module will provide students with a thorough understanding of the core principles of pharmacogenomics and genomic technologies in diagnosing and treating uncommon and hereditary illnesses.

This program combines field training at healthcare institutions with in-person classroom sessions.

Key Information

Campus location        

Languages: English

Study format: Online

Duration: 2-3 weeks

Pace: Part-time 

Tuition fees: Free  

    • Lectures
    • Field visit
    • Tutorial
    • Assignments
    • Log-book completion
    • Final Project Assessment

Applied certificates are designed to serve diverse career opportunities for a range of professions from laboratory-based researchers to diagnostic and healthcare professionals. That includes:

    • Hospital pharmacists
    • Physicians
    • Industrial Pharmacists
    • Molecular biologists
    • Workers in the biotechnology field
    • Community Pharmacist

You will study the following topics in the Pharmacogenomics of Rare and inherited diseases module:

    • Introduction to pharmacogenomics and its application in clinical settings
    • Karyotyping as the first genomic approach
    • Next-generation sequencing and Diagnosis of Genetically Heterogeneous Disorders (Inherited Retinitis Pigmentosa)
    • Molecular Diagnosis and Genetic Counseling of Cystic Fibrosis and Related Disorders
    • Precision Medicine in Cardiovascular Disease
    • Precision Medicine in Cardiovascular Diseases Part II
    • Ethical and Policy Issues around Genome-Wide Association Studies and Biobanks

You must have the following qualifications as a minimum:

    • Sc. in pharmaceutical sciences
    • Sc. in medicine
    • Sc. in biotechnology

You must have the following qualifications as a minimum:

    • B.Sc. in pharmaceutical sciences
    • B.Sc. in medicine
    • B.Sc. in biotechnology