‘Genomics of Common and Rare Inherited Diseases’ - Health Assignment Help

Assignment Task:

Task:

“Technical advances in genetics and genomics have potential to impact upon clinical science and the NHS, for example with developments in whole genome sequencing-based diagnostics. Newborn babies are currently subjected to a blood spot test at day 5 which involves taking a small blood sample to screen for 9 rare but serious health conditions. If you were to employ whole genome sequencing at birth in the population what medical conditions would you consider screening for and how may this result in improvement in patient diagnosis, care and also novel therapy development.”

The assignment for the ‘Genomics of Common and Rare Inherited Diseases’ module will be an essay on the following topic

Please return as word document not exceeding 3000 words (excluding tables, figure legends, and references). Indicate only your student ID number (not name) in the file name and title page.

Provide an Abstract of no more than 250 words and structure the main part of the report to have Introduction, main section addressing the question, and a brief Conclusion section Please use only references from peer-reviewed journals; do not include references from sites that have not been peer reviewed and avoid referencing the lecture you attended as part of this module

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