HelixOvjeren akaunt

@my_helix

We are a population genomics company with a simple but powerful mission: empower every person to improve their life through DNA.

San Mateo, CA
Vrijeme pridruživanja: lipanj 2015.

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  1. Prikvačeni tweet
    9. sij

    Excited for our collaboration with on Tapestry—a study aimed at sequencing from 100K people. Together we'll work to advance research and patient care by providing actionable genetic insights to participants and their providers.

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  2. proslijedio/la je Tweet
    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

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  3. proslijedio/la je Tweet
    1. velj

    Watch the video to learn more about our partnership with !

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  4. 31. sij

    Register now to hear how population genomics has impacted healthcare in Nevada and how it's continuing to advance our understanding of human genetics

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  5. proslijedio/la je Tweet
    31. sij

    "We look forward to working with Mayo to accelerate the integration of genomics into standard patient care and drive novel genetic discovery." - Marc Stapley, CEO. 💬

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  6. proslijedio/la je Tweet

    Study of rare variants in the exomes of more than 70,000 individuals. Justin Kao led a panel on scalable return of genomics, at the PMWC 2020 Silicon Valley.

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  7. 28. sij

    The use of exome sequencing data—as opposed to microarray or lcWGS data—enabled detection of singleton variants (those that occurred only once in the study population) without which 88% of associations would have had a weaker statistical significance.

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  8. proslijedio/la je Tweet
    28. sij

    Fantastic work on genome-wide rare variant analysis in multiple large-scale cohorts!

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  9. 28. sij

    Through gene-based collapsing analysis, and her coauthors were able to identify over 100 gene-phenotype associations, 84% of which would not have been identified if variants had been analyzed using a GWAS approach.

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  10. 28. sij

    See how rare variant analysis on thousands of clinical phenotypes and 70,000+ exomes across independent cohorts ( and ) led to the discovery and validation of a number of novel biomarkers on with

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  11. 22. sij

    How do you move genomics to standard of care? Find out at 2:00 pm today as leads a discussion panel on the state of genomics and healthcare.

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  12. proslijedio/la je Tweet
    21. sij

    Proud to welcome the leadership of to as we plan strategies for the Project for 2020.

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  13. proslijedio/la je Tweet
    20. sij

    Could preemptive genetic testing help provide important information about disease risk and allow for better preventive care? Learn how a collaboration between Mayo Clinic and Helix is aimed at answering that question. Clinic

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  14. proslijedio/la je Tweet
    17. sij

    Mayo Clinic, Helix collaborate to better understand how whole exome sequencing may impact health care by providing information about disease risk and allow for better preventive care Clinic

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  15. 17. sij

    Happy to see highlighting our work in population . We’re enabling ongoing disease screening, precision health, and novel genetic discoveries.

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  16. proslijedio/la je Tweet
    17. sij

    . says it is creating a library of genomic sequencing data on 100,000 consented Mayo Clinic participants to advance research and patient care

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  17. 16. sij

    What does it mean to inherit a risk for CDC Tier 1 conditions? We found that it correlates with a 30 year acceleration of disease onset. Learn more from and in this upcoming webinar about our findings from

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  18. 13. sij

    On Jan. 22nd, Sarah Bobulsky, Senior Director of Commercial at Helix will be joining the team at to discuss her career path and to chat about the process of defining your role within a startup. Sign up today and submit questions here:

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  19. proslijedio/la je Tweet
    13. sij

    assoc. dir. explains how the initial study in a new collaboration between and could help diagnose hereditary and

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  20. proslijedio/la je Tweet
    11. sij

    collaboration to build a genomic library could reveal predispostitions to disease and allow for earlier use of throughout a person's lifespan.

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  21. proslijedio/la je Tweet
    10. sij

    Learn more about Tapestry, the new clinical study from & . The project aims to sequence 100k Mayo Clinic patients to create a library of genomic sequencing data to advance research & patient care.

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