www.hee.nhs.uk masters programme in genomic medicine open day event tendering process anne gilford,...
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Masters Programme in Genomic Medicine Open Day Event
Tendering process
Anne Gilford, Head of Education and Quality, HEWM
3rd September 2014
Masters Programme in Genomic Medicine Open Day Event
MSc Genomic Medicine Curriculum
Val Davison, Scientific Advisor, National School of Healthcare Science
10 November 2015
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HEE/GeL Masters (MSc) Programme in Genomic Medicine
Support 100,000 genomes
project and the research &
clinical opportunities it
provides
Transformation of both
specialist and general work
force
Wider education in
genomic medicine
Multiprofessional - build
sustainable capacity within
the NHS
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Development of MSc
MSc – full curricula available
with tender
Developed by experts from both GE and
HEE
Academic and clinical input
Also out to consultation with patients and public
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Commissioning
• MSc Genomic Medicine delivered in South West geographical footprint
• Track record of teaching at postgraduate level• Demonstrate potential partnerships with Genomic
Medicine Centres • Required to form a national network and work
collaboratively • 65 commissions to be allocated to successful for full
Master’s• 100 CPPD commissions to be allocated
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Programme Structure
• A full time option delivered over 1 year • P/T – 2 years blended learning format • Access to individual modules CPD• Combinations of credit modules that can lead to PG Cert or
PG Diploma • A significant research component in the MSc• Flexibility delivered by core modules and optional modules
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Programme Structure
Core Modules 15 credits
• An introduction to genomics• Omics techniques and their
application to medicine • Genomics of common and
rare disease • Molecular pathology of cancer • Pharmacogenetics and
stratified healthcare• Application of Genomics to
infectious disease• Bioinformatics interpretation • Research dissertation (60 /30
credits)
Optional Modules 15 credits
• ELSI• Counselling skills for
genomics• Economic models and
genomics• Workbased learning • Professional and research
skills • Epigenetics
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Research modules
• Research project (60 credits)– Education and Training GeCIP led by HEE– In house project
• Clinical • Laboratory based
• Literary dissertation (30 credits)– Epigenetics – Clinical topics
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Potential Module Combinations
Modules
Core modules 1-7
Research Module
Optional modules
Total Credits
Combination 1
7x15 = 105 credits
1x60=60credits
1x15=15credits
180 credits
Combination 2
7x15=105 credits
1x30 = 30 credits
3x15=45 credits
180 credits
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• Discuss the human genome structure and the properties of DNA sequence
• Critique the regulation of gene expression, transcription and translation and the contribution of each to cellular phenotype
• Discuss critically epigenetic modifications and imprinting and role in disease
• Describe the correlation of genotype with phenotype for both dichotomous and quantitative traits
• Describe and evaluate the purpose, structures, use and storage of health records
An Introduction to Human Genetics and Genomics
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Omics Techniques and application to genomic medicine
• Describe and critically evaluate a range of sequence technologies to targeted parts of the genome or whole genomes
• Discuss how these techniques and their applications in RNA expression, metabolomics and proteomic analysis
• Discuss and criticially appraise approaches to the bioinformatics analysis and interpretation of ‘omics’ data
• Critically evaluate the different ‘omics’ technologies and platforms in relation to genomic medicine
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Genomics of common and rare disease
• Explain the principles of the genetic architecture of common and rare diseases
• Critique traditional and current approaches used to identify genes for common and rare diseases
• Discuss the Genomics England Programme and the Data Infrastructure
• Identify phenotype, select cases and relevant family information for whole exome or whole genome based approaches for hypothesis free whole exome or whole genome sequencing.
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Pharmacogenomics & stratified health-care
• Discuss and evaluate the mechanism of several examples of genomically-determined differential drug response, and drug reaction
• Critique the strategies and analytical approaches for stratifying patients for adverse drug reactions or optimal drug response, including ethnic differences, and how these translate into ‘companion diagnostics’
• Discuss critically with examples, how genomic information can enable development of drugs targeted for particular genotypes
• With reference to examples, demonstrate an appreciation of the ELSI which could accompany patient
stratification for healthcare advice or intervention.
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: Application of genomics in Infectious disease
• Demonstrate an in-depth knowledge of the differences between prokaryotes and eukaryotes genomes
• Discuss how the genome sequence of pathogens can be used to track cross infection and outbreaks of infections among the population
• Critique the molecular basis of organism drug resistance in some infections and how this directs drug research
• Evaluate how sequencing of the genome of infective organisms can be used in infectious disease for assessing: diagnosis, sub-classification & strain identity, pathogenicity, drug resistance and drug selection; and for epidemic control.
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Clinical Bioinformatics • Discuss the principles applied to quality control of sequencing
data, alignment of sequence to the reference genome, pathogenic mutations in sequencing data
• the principles of informatics and bioinformatics applied to clinical data, and gain practical experience of the major national and international resources and standards which underpin them
• Discuss Iinterrogate major datasources, e.g. of genomic sequence, protein sequences, variation, pathways, (e.g. EVS, dbSNP, ClinVar, etc.) and be able to integrate with clinical data, to assess the pathogenic significance of genome result
• Acquire computational skills • Gain practical experience of the bioinformatics pipeline through
the Genomics England programme• Understand the place of Professional Best Practice Guidelines in the diagnostic setting for the reporting of genomic variation.
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Making sense of the science……..
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