ClinGen

@ClinGenResource

Sharing Data. Building Knowledge. Improving Care.

clinicalgenome.org
Clárú: Bealtaine 2013
26 Pictiúr nó físeán Pictiúir agus físeáin

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  1. Rinne Atweetáil
    19 Iúil

    There is a pressing need for data sharing to help in human genomic variant interpretation.

    , , agus
    22 d’atweetálacha 22 croí
  2. Rinne Atweetáil
    17 Iúil

    Uploading your report - what if you do not have a copy? Email us a and we will help!

    4 atweetáil 4 chroí
  3. 14 Iúil

    Listen to on GenePod, Making sense of a deluge of variants: harnessing the power of community

    12 d’atweetálacha 12 croí
  4. 14 Iúil

    ClinGen recognizes labs sharing their data - see commentary by in

    1 fhreagra amháin 12 d’atweetálacha 18 croí
  5. Rinne Atweetáil
    6 Iúil

    's monthly data release is now available: ftp://ftp.ncbi.nlm.nih.gov/pub/clinvar/release_notes/20170706_data_release_notes.pdf

    2 atweetáil 2 chroí
  6. 30 Meith

    Thanks to everyone who made a success! See you in Hinxton next May for

    2 atweetáil 6 chroí
  7. 30 Meith

    Thank you to the meeting silver sponsors

    3 atweetáil 6 chroí
  8. 30 Meith

    Thank you to the Curating the Clinical Genome meeting platinum sponsors

    1 atweetáil amháin 4 chroí
  9. 30 Meith

    Final session, Functional Genomics Aiding Clinical Interpretation

  10. 30 Meith

    Don't miss the workshop this morning, learn about their tools for variety interpretation and data sharing

    1 atweetáil amháin 3 chroí
  11. Rinne Atweetáil
    30 Meith

    Deb Ritter getting a lot of interest in standards for somatic variants.

    1 fhreagra amháin 1 atweetáil amháin 2 chroí
  12. 29 Meith

    Thanks to our presenters! Now go visit these and all the other fantastic posters in our session!

    1 chroí
  13. 29 Meith

    We want to hear what you thought of the Rapid Platform session, was it a hit?

    1 chroí
  14. 29 Meith

    The first ever Rapid Platform Session is about to begin! 18 poster presenters - one slide and one minute each!!

    1 chroí
  15. 29 Meith

    Evolving Guidelines/Resources to Support Variant Assessment off to a great start with &

    1 atweetáil amháin 5 chroí
  16. 29 Meith

    Return of Results session spans the hereditary cancer, community health and prenatal setting

    1 atweetáil amháin 1 chroí
  17. 29 Meith

    Thank you to our speakers this morning, great to hear from

    2 atweetáil 5 chroí
  18. Rinne Atweetáil
    29 Meith

    Read workshop report on the classification and interpretation of human genome variants.

    , agus
    16 d’atweetálacha 15 croí
  19. 29 Meith

    starts off today at 8amET with sessions on Curating Gene-Disease Relationships and Perspectives and Regulations on Data Sharing

    2 atweetáil 5 chroí
  20. 29 Meith

    Thank you for joining us!

    Lively & educational discussion tonight at Curating the Clinical Genome conf. Thanks for inviting me to speak, .
    3 chroí

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