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Category: Socialising the Genome

Global perspectives on health, research and trustworthiness

Trust is critical to virtually everything we do in life, wherever in the world we are. We trust that when … More

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Data, data sharing, DNA, ethics, Genomics, health data, Research, Society and Ethics Research, Survey

An Important Era for Socialising the Genome

Genomics, Public Trust and Engagement “Genomics” – a scientific term previously considered most relevant to scientific research, is now a … More

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Data, data ethics, data sharing, DNA, ethics, Genomics, public engagement, socialising the genome, Society and Ethics Research

Future of Genomic Research at Risk Without Greater Public Trust in How Genetic Data is Shared, Survey Finds.

The largest ever survey on global public attitudes towards genomic research and data sharing suggests that work is needed to … More

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Data, Genome Research, Genomethics
Articulating the contract between science and people: DNA data sharing

Articulating the contract between science and people: DNA data sharing

A new deal on data: are you with us? For most of us it is hard to unpick the various … More

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Anna Middleton, Consent, Data, Data - Big, DNA, Genome Research, Genomethics, Legal, Research, Research participant, Scientists, Society and Ethics Research
Genomethics Blog - Illustration (Original)

Socialising the Genome – how do we start a conversation about genomics?

How easy is it to strike up a conversation about genomics? Geno-what? Does the average person on the street know … More

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Data, Genetic Testing, Genomics, Healthcare, NHS
DNA Sequencing – Can You Handle the Truth?

DNA Sequencing – Can You Handle the Truth?

Having your genes studied  is cheap (about $99) and easy (just spit here). And according to 23andMe (one of the … More

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Genetic Testing

Recent Posts

  • The Character of science: can what we see on a reel be translated to real-life?
  • The Evolution of the Genetic Counselling Profession
  • Global perspectives on health, research and trustworthiness

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Anna Middleton PhD

Head of Society and Ethics Research, Connecting Science at Wellcome Genome Campus, Cambridge, UK. Chair of Association of Genetic Nurses and Counsellors. Continually asking 'how are people making sense of genomics?'


 

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