discuss the introduction of whole genome sequencing at birth i.e. expanding the

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discuss the introduction of whole genome sequencing at birth i.e. expanding the current newborn screening of 9 genetic diseases. .
I have added some references that I think would be useful and that was suggested
So you need to cover the current UK National Screening programme for newborns, a brief outline of whole genome sequencing and discuss in more detail about limitations of WGS and challenges in non-symptomatic babies. You then need to discuss in a broader way the type of diseases you propose to include on top of the 9 rare but serious health conditions in the current test and why e.g. should they meet certain criteria. You need to briefly cover ethical considerations around newborn screening by NGS

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