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Der Phänotyp-Broker: Blockchain und Patienten-Phänotypen

Posted on by by Posted in Allelische Variante, In der Zukunft, Personalisierte Medizin, Personomik, Thasso Post, Theragenomische Medizin No Comments ↓

27. Juli 2019 – “Blockchains for secure digitized medicine”. Dies ist der Titel eines sehr interessanten und wichtigen Artikels im Journal of Personalized Medine (JPM) vom 28. Mai 2019.

Blockchain als aufstrebende Technologie (insbesondere im Zusammenhang mit dem Hype um Bitcoins) hat an Popularität gewonnen,

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RSS random genetics

  • Ancestry launches DNA health service that will compete with 23andMe October 15, 2019
    Ancestry has long appealed to people eager to learn about their family roots. Now the company known for its popular DNA kits is diving into a new area of discovery—health.
  • Improving research with more effective antibodies October 15, 2019
    A new study points to the need for better antibody validation, and outlines a process that other labs can use to make sure the antibodies they work with function properly.
  • New DNA 'clock' could help measure development in young children October 15, 2019
    Scientists have developed a molecular "clock" that could reshape how pediatricians measure and monitor childhood growth and potentially allow for an earlier diagnosis of life-altering development disorders.
  • DNA fracturing rewires gene control in cancer October 15, 2019
    Understanding the mechanisms that mediate widespread DNA damage in the cancer genome is of great interest to cancer physicians and scientists because it may lead to improved treatments and diagnosis. In this study, a multi-institutional team led by researchers at Baylor College of Medicine has brought attention to genomic structural variation as a previously unappreciated […]
  • Most genetic studies use only white participants – this will lead to greater health inequality October 15, 2019
    Few areas of science have seen such a dramatic development in the last decade as genomics. It is now possible to read the genomes of millions of people in so-called genome-wide association studies. These studies have identified thousands of small differences in our genome that are linked to diseases, such as cancer, heart disease and […]
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