Rezultati pretraživanja
  1. Fantastic news that we’ve sequenced 100,000 genomes - as pledged 5 years ago. Genomics is the future - it’s bigger than Brexit - and Britain leads the world

  2. 11. pro 2018.

    NWC 100,000 genomics team in London for celebration event today following the 100,000 target reached last week - onwards to 5 million

  3. Best part of the day: hearing from these three participants from about taking part in . I shed a tear hearing about Cuthbert’s contribution.

  4. Congratulations to on their milestone 100,000th genome sequenced . This incredibly valuable project is already delivering life-changing benefits for some patients with rare diseases 👏🏻

  5. 17. pro 2018.

    'He’d asked for a test for his tinsellitis, But the genome had answered a lot more besides this' Some great rhyming on this seasonal poem about sequencing Santa. But what I want to know is which GMC recruited him to ?

  6. 20. sij

    The genomes for all Scottish families in have now completed initial review by & most have been analysed by . But bear with us if you're waiting for results... lots of checks still needed by NHS Scotland Genetics

  7. The achievement is world leading. It would not have been possible without the collaboration and hard work of everyone involved especially participants and their families. Lets keep up the momentum!

  8. 11. pro 2018.

    “An unprecedented achievement with life changing results” Dame Sally Davies summing up the 100k Genomes Project perfectly!

  9. 4. velj

    NEW! We conducted qualitative interviews with 20 parents participating in the 100,000 Genomes Project to find out about their motivations, concerns & understanding of genome sequencing. You can read the open-access paper here:

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  10. 11. pro 2018.

    Two key inspirational Dames continuing to drive Genomics forward within our wonderful Service.

  11. Great morning with and at with lots of interesting discussions and viewpoints on informing policy on secondary genetic findings. Learnings from the Honour as always to add a patient voice

  12. 20. ožu 2019.

    speech by strongly emphasises the ethical Qs raised by genomics. Need to find the right balance re helping people take responsibility for health and advancing research, and ensuring people are supported and their data protected

  13. 11. pro 2018.

    Celebrating completion of recruitment to the recognising the contribution of ⁦⁩ ⁦⁩ ⁦⁩ ⁦⁩ for the benefit of patients across ⁦⁩ ⁦⁩ ⁦

  14. 11. pro 2018.

    Great to have the opportunity again to meet to celebrate our achievements!

  15. Absolutely delighted the UK has achieved my pledge of sequencing 100,000 whole genomes. We are leading the world in genomics – and changing the lives of those with rare diseases and cancer. Thank you to everyone involved

  16. 11. pro 2018.

    'I want us to be the health service that delivers genomics'. Prof Dame Sally Davies

  17. "I wish I was a young pharmacologist right now." John Mattick, CEO of , spoke at this week. He told us afterwards about his excitement about the future of precision medicine.

  18. 22. ožu 2019.

    Ethics can support, rather than hinder, science and medical progress - writes about the importance of placing ethics at the heart of healthcare initiatives

  19. 5. ožu 2019.

    Great evening speaking with these guys about our experiences as patients or parents of patients going through genomic testing. Nice to see so many healthcare professionals in the room interested in our thoughts

  20. 6. pro 2018.

    We are pleased to announce that we have now sequenced 1,000 samples as part of the Project, which aims to improve outcomes for patients by using clinical and genomics data. We look forward to continuing this valuable work with in future

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