We live in an exciting time where we can easily sequence entire genomes. This, coupled with advances in Artificial Intelligence (AI), has driven significant development in bioinformatics methods - the tools we use to study the sequence information. You will explore state-of-the-art bioinformatics and genomics tools, with a strong focus on practical application of these tools to answer important biological questions. You will combine information from multiple tools to gain detailed knowledge and understanding in the intrepretation of results from bioinformatics and genomics resources, particularly in understanding how genetic variants are associated with disease.
Lecture 12 hours, Computer Workshop 18 hours, Feedback Session 2 hours
Short answer questions and 750 words extended answer Short Writing Piece. Assessment Details: Case Study worth 30%.
1,500 words Report . Assessment Details: Individual Report worth 70%.
Reassessment Method: Like-for-like
On successfully completing the module, students will be able to:
1. Appraise the wide range of bioinformatics and genomics tools that are available for analysis of both genomes and proteins.
2. Apply advanced web-based tools and software to analyse protein structure and function.
3. Apply advanced web-based tools and software to analyse genetic variation in the human genome and how it may alter protein structure and function.
4. Evaluate data obtained from multiple such tools (from 2 and 3) to generate hypotheses about how genetic variants may be associated with disease.
University of Kent makes every effort to ensure that module information is accurate for the relevant academic session and to provide educational services as described. However, courses, services and other matters may be subject to change. Please read our full disclaimer.