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Joined March 2014
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Today is #DNA Day. To celebrate, we’re offering a special discount to uncover what your DNA can reveal. Take control of your health and screen for 15,000+ diseases and conditions.
There are currently thousands of rare diseases. Most are genetic. Many affect children.
Individually, each one is statistically improbable. Collectively, they affect tens of millions of people.
The odds of two siblings having the exact same genetic makeup: less than 1 in 70 trillion.
You are, quite literally, a one-time event in human history.
Your entire genetic instruction manual is written in just 4 letters: A, C, G, and T.
You have 6 billion of them packed into nearly every cell in your body.
A change in just one can be the difference between health and a genetic disease.
"Globally Sequencing.com’s impact extends far beyond individual users and organizations. By providing an open operating system for DNA innovation, they have unlocked a world of possibilities for researchers, developers, and entrepreneurs."
techventure.news/startup-sho…
Genome Sequencing Appears to Edge Out Exome Sequencing in Clinical Utility in Meta-Analysis.
genomeweb.com/scan/genome-se…
Sequencing retweeted
Being #undiagnosed can prevent patients from participating in clinical trials, receiving assistance for treatment or care, & connecting w/others facing similar experiences. Let’s change the #diagnosticodyssey & the future of medicine. #UndiagnosedImpactCampaign #UndiagnosedFilm
Within a few weeks of the public announcement from NBCI, the Sequencing.com team has already updated our platform with the newest dbSNP release.
Build 156 includes has over 1.1 billion RefSNP (rs) records across the human genome.
Sequencing retweeted
Yesterday was #RareDiseaseDay.
We would like to sincerely thank 🙏 everyone that took part in the campaign! We invited you to #LightUpForRare✨ and to #ShareYourColours💙💚💜 and you answered our call beautifully.
Together let's continue advocating for a more equitable society!
"For rare disease patients, a diagnosis, even one with a poor outcome, is often a luxury—long sought after, hard won, and, in a worst-case scenario, forever elusive. The average time to diagnosis, if one can be found: eight years. "
fortune.com/well/2023/02/28/…
So we asked chat CPT to write a tweet for us to explain whole genome sequencing.
“Whole genome sequencing is like a full body scan for your DNA. It can reveal genetic risks for diseases, as well as help with personalized medicine.”
Thoughts?
This capital raise allows us to rapidly expand our unique solutions that unlock the true value of genetic data and directly empower the individual
via @erinbrodwin in @axios
axios.com/pro/health-tech-de…
Sequencing retweeted
.@SequencingCom provides “Whole Genome Sequencing” to consumers affordably and securely for the first time, helping individuals take control of their health and optimize for better health outcomes.
lererhippeau.medium.com/plea…
Great article from @royfurchgott. We are waiting for the day when whole genome sequencing can cost $100.
nytimes.com/2022/10/12/busin…
✨ Want to test the latest and greatest version of Genome Explorer for free?
Now accepting beta testers!
To become a beta tester, please email [email protected].
The requirement is that you have at least one DNA data file stored in your account.
A great explanation on why a gapless sequence of a human genome was so difficult.
When Human Genome Project researchers announced they had successfully completed sequencing the human genome, it was only about 92% complete. There were still hundreds of gaps or missing DNA sequences. Why was it so difficult to complete the sequence? Let’s break it down! #T2T
The DRD1 gene has been linked with anorexia. Incredible research has shown that this may be able to be reversed.
neurosciencenews.com/dopamin…
#anorexia #genetics #genomics #dna #sequencing neurosciencenews.com/dopamin…
