Rezultati pretraživanja
  1. prije 7 sati

    Comprehensive T cell repertoire characterization of non-small cell lung cancer

  2. 1. velj

    Population-scale efforts, improve our understanding of the human . Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts

  3. 29. sij
  4. A SOM team found that trio exome for fetal structural anomalies has significant diagnostic utility when a diagnosis was suspected. Read about what this could mean for clinical practice in their in Medicine paper here:

  5. 27. sij

    This article will give you some idea of how to be intentional about your career. However, I would add , which is determining the order in which the work is done.

  6. 9. sij

    Our understanding of both common and rare diseases is flourishing. Improvements in technology and are allowing researchers to link mutations and diseases faster than ever, paving the way for prevention and precision medicine.

  7. 9. pro 2019.

    Coupling chemical mutagenesis to next generation sequencing for the identification of drug resistance mutations in Leishmania

  8. Before we got to the final version of our 3D video on & , we needed a storyboard! Special thanks to our art editors Lara Crow and Pat Morgan for their brilliant ideas

  9. Have you watched our new on next-generation and yet? A great collaboration with , sponsored by

  10. 28. lis 2019.

    "We now are at the point where I think the evidence is overwhelming that a rapid genome sequence can save a child's life." Dr. Stephen Kingsmore spoke to about how newborns in intensive care can benefit from rapid whole genome .

  11. 25. lis 2019.

    check out our new article providing new insights into using . In collaboration with & labs, spearheaded by &

  12. 6. lis 2019.

    : from imagination to reality. This short manuscript is always a very nice reading and explains that sometimes important tools need decades to be developed!! 😃

  13. 30. kol 2019.

    Not all heroes wear capes. Great story in about the inspiring quest of & “to bring a genome to every kid who needs one” and use genomic to give hope & answers to families facing rare genetic disease.

  14. New online from Dzunkova et al.: Utilizing a single-cell tagging & approach to identify host - interactions from the human gut :

  15. Playing a long game: finds its footing and ‘next-wave’ applications are emerging. Read our August tech feature here.

  16. New online from Sanchez-Buso et al.: of global isolates finds modern strains emerged relatively recently & split into two lineages with differential susceptibility:

  17. New online from David et al.: European -resistant pneumoniae isolates suggests extensive within-hospital spread & increased transmission of strains with higher degrees of :

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  18. 8. srp 2019.

    "If reveals health risks at any point in life, and if that's good, then it's better to do it early," says , MD, MPH, geneticist and physician at the Brigham.

  19. Great work! Read about how uses transportable to identify potentially pathogenic bacteria in the river Cam Findings will be published in the summer. ​ HT

  20. 28. velj 2019.

    news for : ~10% of babies tested with had risks for actionable, childhood-onset conditions, incl 1 infant who started simple treatment & is now a 2yr old!

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