When Noah began having cardiac arrests at 18 months old, his doctors couldn’t figure out why. An exome sequencing test helped reveal the genetic source of his cardiac arrests and gave his parents more certainty about how to protect his health. Read Noah’s story here: https://invit.ae/3Y4hNJD #SCAmonth
Invitae
Biotechnology Research
San Francisco, CA 145,101 followers
Bringing comprehensive genetic information into mainstream medicine to improve healthcare.
About us
Invitae, now part of Labcorp, is a leading medical genetics company trusted by millions of patients and their providers to deliver timely genetic information using digital technology. We’re working to provide accurate and actionable answers to strengthen medical decision-making for individuals and their families. Invitae's genetics experts apply a rigorous approach to data and research, serving as the foundation of our mission to bring comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. Within each of us lies information coded in our DNA that can transform our health. Unlocking that potential requires highly specialized, multidisciplinary collaboration. Our world-class genetics experts drive the development of a highly complex system of tools and processes, including robotics, artificial intelligence, machine learning, and software engineering. All of this comes together to provide patients with accurate, reliable results that can help guide decisions across the healthcare journey and potentially change lives today and for the next generation. Our teammates are grounded in a universal sense of urgency and ownership. We believe in the team above the individual and celebrate freedom with accountability. Employees are encouraged to speak up, try new things and make decisions that push us forward. We provide all Invitaens with opportunities to grow and advance, supported by flexible work hours, unlimited paid time off, the ability to work anywhere for many roles and the satisfaction of doing meaningful work. At Invitae, we're putting patients' genetic insights where they belong—at the center of healthcare. And we're doing it together, with you. Join us.
- Website
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http://www.invitae.com/
External link for Invitae
- Industry
- Biotechnology Research
- Company size
- 1,001-5,000 employees
- Headquarters
- San Francisco, CA
- Type
- Public Company
- Specialties
- genomics, biotechnology, healthcare, oncology, cancer, cardiology, rare genetic disease, neurology, hematology, pediatric genetics, and genetic testing
Locations
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Primary
1400 16th Street
San Francisco, CA 94103, US
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1400 16th St
San Francisco, CA 94103, US
Employees at Invitae
Updates
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As we honor and support survivors and patients during Breast Cancer Awareness Month, take a moment to explore how #genetictesting can be a powerful tool for helping your patients take care of their health. Learn how we make testing easy: https://invit.ae/3XXM50o #BCAM
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There’s still time to register. Join us for this live webinar presented on October 10 at 12 pm ET/9 am PT and earn CEUs by attending. Register: https://invit.ae/4ek1Buw #genetictesting #GCchat
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Interested in exploring Sherloc? Join us for a live webinar presented on October 10 at 12 pm ET/9 am PT and earn CEUs by attending. Register now: https://invit.ae/4ek1Buw #genetictesting #GCchat
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Are you testing all of your ovarian cancer patients? Learn more about #genetictesting recommendations for your patient. https://invit.ae/4erpZdU #OvarianCancerAwarenessMonth
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The evolution of Sherloc: Insights into the innovative and scalable approaches impacting variant classification. Join us for this live webinar presented on October 10 at 12 pm ET/9 am PT and earn CEUs by attending. Register today: https://invit.ae/4ek1Buw #genetictesting #GCchat
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Congrats to ClinVar on reaching their 3 million milestone. This free, public database gathers information on genomic variations and their impact on human health. We're the #1 contributor, having submitted over 1.7 million genetic variant entries as of June 2024, aiming to promote transparency and improve patient care. Learn more about how we do it: https://invit.ae/3zK2pJA National Center for Biotechnology Information (NCBI)
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Ninety-five percent of rare diseases lack approved treatments. Better and deeper genetic datasets can help researchers make data-informed decisions as they strive to meet this urgent medical need. Learn how our huge set of de-identified patient data is helping #biopharma companies develop much-needed novel therapeutics. https://invit.ae/4exQkXk
Rare disease research benefits from large clinical and genomic datasets
blog.invitae.com
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Genetic counselors are such a crucial part of a healthcare team, providing important information and support to patients and their families about their genetics. We’re thrilled about this positive step forward to ensure their services are captured accurately and consistently and to aid in health claims. Congratulations to everyone on this hard-won success. #GeneChat #NSGC24
🧬NEW: Genetic counselors have a new CPT® Code: 96041 launching January 2025! This is a positive step for our profession, ensuring genetic counselors can serve as vital healthcare partners for our provider colleagues and patients. Under the new code, billing will be based on the "total time” provided by the genetic counselor on the date of the encounter. In the coming weeks, NSGC will engage with members and external partners, including payors, starting with a can’t-miss plenary session on Sept. 19 at the #NSGC24 Annual Conference. We thank our volunteer and consultant teams, as well as ACMG - American College of Medical Genetics and Genomics for their efforts to help ensure that we can continue to deliver crucial services to our patients. Stay tuned for more resources as we transition to the new code going live in January 2025. #GeneChat