Human Genetics Bachelor of Science (with Honours) - BSc (Hons)
Course Overview - Human Genetics Bachelor of Science (with Honours) - BSc (Hons)
Human genetics is central to health, medicine, and pharmacology, and our BSc (Honours) Human Genetics degree is designed to provide you with a comprehensive grounding in this ever-evolving subject.
Recent advances in biology have led to a better understanding of how genetic variations affect genome function and influence traits, which, in turn, has led to increased job opportunities for graduates with skills in human genetics.
The human genetics course will introduce you to the study of molecular biology and explore the fundamentals of:
• evolution and ...
Human genetics is central to health, medicine, and pharmacology, and our BSc (Honours) Human Genetics degree is designed to provide you with a comprehensive grounding in this ever-evolving subject.
Recent advances in biology have led to a better understanding of how genetic variations affect genome function and influence traits, which, in turn, has led to increased job opportunities for graduates with skills in human genetics.
The human genetics course will introduce you to the study of molecular biology and explore the fundamentals of:
• evolution and its impact on genetic differences\
• medical microbiology\
• biochemistry\
• genetics of diseases.
Throughout the course, you will acquire the knowledge, skills and behaviours to excel in research, industry and academia.
What you'll study
Through this course, you will gain a critical understanding of the connections between human genes, the human body and hereditary variations.
As well as learning and fine-tuning your clinical, industrial and research abilities, you will develop techniques to solve modern-day problems such as human disease and threats to population health.
The course will enable you to:
• gain the knowledge and skills to examine samples of patients' nucleic acid (DNA or RNA (Ribonucleic acid)) to identify genetic and genomic alterations that may be responsible for inherited and acquired diseases or conditions, such as cystic fibrosis, sickle cell disease or cancer\
• practice the skills for prenatal diagnosis - examining cells for possible anomalies in the foetus, usually in families where single-gene disorders have been identified by DNA analysis\
• understand carrier testing and risk assessment for identifying presymptomatic individuals at risk from single-gene disorders\
• learn confirmation of diagnosis in both inherited and acquired conditions.
You will also benefit from:
• excellent facilities, including new biomedical science labs\
• regular promotion of work experience opportunities as well as workshops preparing you for working as a geneticist, including interview techniques, work placements, and negotiating workplace politics\
• seminar series with bodies such as Genomics England Clinical Interpretation Partnership (GeCIP), evidence workshops and seminars\
• mentoring programme between students of all years\
• UWL's strong links with local healthcare providers and biotech industries.
Course Information
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Course Details
Information
Study Mode
Full-time
Duration
3 Years
Start Date
2027-09-01
Campus
Main site - West London
Application Details
Provider Details
Codes/info
Course Code
A65-A68
Institution Code
W05
Points of Entry
Year 1
Entry Requirements
A level
UCAS Tariff
Access to HE Diploma
Pass Access to HE Diploma (Minimum of 45 credits at level 3)
Pearson BTEC Level 3 National Extended Diploma (first teaching from September 2016)
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