

SGUL - Interpreting Genomic Variation: Inherited Cancer Susceptibility
- Offered byFutureLearn
Interpreting Genomic Variation: Inherited Cancer Susceptibility at FutureLearn Overview
Interpreting Genomic Variation: Inherited Cancer Susceptibility
at FutureLearn
Duration | 2 weeks |
Total fee | ₹8,364 |
Mode of learning | Online |
Credential | Certificate |
Interpreting Genomic Variation: Inherited Cancer Susceptibility at FutureLearn Highlights
Interpreting Genomic Variation: Inherited Cancer Susceptibility
at FutureLearn
- Earn a certificate of completion from Futurelearn
Interpreting Genomic Variation: Inherited Cancer Susceptibility at FutureLearn Course details
Interpreting Genomic Variation: Inherited Cancer Susceptibility
at FutureLearn
More about this course
- On this course, you will consider how variant interpretation in cancer susceptibility genes has different considerations when compared with variant interpretation in rare paediatric disease
- You'll explore the guidelines produced by the UK Cancer Variant Interpretation Group (CanVIG-UK) for variant interpretation and how these can be applied to the American College of Medical Genetics (ACMG) framework in the classification of germline variants in cancer susceptibility genes
- This course will provide you with patient examples to explore the complexities of variant interpretation in cancer genomics
- You'll also hear from experts in the field about how the CanVIG-UK guidance was created
- You'll be encouraged to apply your learning through case-based exercises that illustrate both the strengths and weaknesses of the tools and guidelines available for cancer variant interpretation
Interpreting Genomic Variation: Inherited Cancer Susceptibility at FutureLearn Curriculum
Interpreting Genomic Variation: Inherited Cancer Susceptibility
at FutureLearn
Cancer susceptibility gene variant interpretation
Introduction to the course
Why is variant interpretation different in Cancer Susceptibility Genes (CSGs)?
Adapting the ACMG framework for CSGs
Population data
Computational and predictive data
Cancer susceptibility gene variant interpretation
Introduction to Week 2
Functional data
Allelic data
Reputable sources
Other data
Other considerations
Pulling it all together
Putting it into practice
The evolving landscape
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Interpreting Genomic Variation: Inherited Cancer Susceptibility
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