Module - Human Genetics HSOB5004
This module encompasses the organisation of the human genome the basis of genetic variation, relationship between mutations in or near genes and the manifestation of disease phenotype. Variations in human genomes and their consequences (monogenic and polygenic disorders) will be discussed including epigenetic effects, comprising the role played by non-coding RNAs.

On successful completion, you will be able to:
- Demonstrate comprehensive knowledge of genetic variation, how it arises and how it can be exploited.
- Demonstrate knowledge of the diverse scientific fields that encompass human genetics including clinical genetics, biochemical genetics and pharmacogenetics.
- Critique the development of new and emerging procedures and techniques.
- Access and evaluate information from a variety of sources and communicate the principles in a way that is well organised and topical.
- Biological significance of coding and noncoding DNA
- Human genetic variation: AT, GC rich sequences, tandem repetitive elements, centromere and telomere structure and function.
- The biology and pathology of sex chromosomes: X inactivation (Barr Body), role of X and Y chromosome in disease onset and detection.
- Complex inheritance and disease: susceptibility genes, twin concordance, familial segregation, linkage analysis.
- Typical approaches used in analysis: immunofluorescence and CGH microarray, next generation sequencing.
- Immunogenetics: HLA typing and genetic immunodeficiency.
- Epigenetics and genomic imprinting: chromosomal modification and methylation patterns, Prader Willi and Angellman syndrome.
- The genetics of the aging process: oxidative damage and telomere function.
- Cancer genetics in brief.
- The commercialisation of genetic information: gene therapy and single nucleotide polymorphisms (SNPs) as both indicators for forensic phenotyping and determining susceptibility to disease.
- Genetic Counselling and Ethical considerations.
Modules are delivered in person, through a blend of lectures, seminars, and practical sessions.
You’ll benefit from close interaction with tutors and peers, access to specialist laboratories, and small-group teaching.
Assessment varies by module but may include:
- Written coursework
- Exams
- Practical assessments
- Case-based evaluations
Each module typically carries 20 academic credits and is completed over one semester.
• Hold a relevant honours degree in biomedical science or a closely related subject.
• Have completed a formal IBMS degree assessment that identifies academic shortfalls.
• Be aiming for HCPC registration as a biomedical scientist.
• Applicants should refer to their IBMS assessment letter when selecting modules.
• Please note these modules do not include a placement, they are intended to address academic learning outcomes only.
20 credit module pricing
Tuition fees are set annually and are subject to review each year. The University may therefore raise tuition fees in the second or subsequent years of a course, in line with inflation and/or the maximum permitted by law or government policy. Students will be notified of any changes as soon as possible.
Location
Carlisle - Fusehill Street Campus
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