Sequencing

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.

"Rare" diseases affect 1 in 10 Americans. 1 in 13 don't even know it yet.

"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-showca…

Genome Sequencing Appears to Edge Out Exome Sequencing in Clinical Utility in Meta-Analysis. genomeweb.com/scan/genome-se…

@medifindhealth uses the power of big data to connect patients with the right doctors and treatments faster. Their mission naturally aligned with our goals. We are so excited to have Medifind help us educate the impact of WGS on people trying to access the best preventive care

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.

@DevinShuman @3TomatoesShort Hi Devin, we provide whole genome sequencing services and help our customers obtain data on 100% of their genome.

@DevinShuman @GeneticCouns Hi Devin, Dr. Colby is a licensed medical physician with expertise in personal genomics and predictive medicine. He has been an associated member of NSGC for more than 7 years and sees patients for genetic counseling. Thank you for correcting the membership status with NSGC.

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/2023/02/2…

Register today for #RareDiseaseDay at @NIH and join NCATS, @DRDRI_NCATS and the @NIHClinicalCntr to learn more about #RareDiseases research on Feb. 28: bit.ly/3UScU2p 1/2 #RDDNIH

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?

@LisaHandwovens @stcohen112 @hola_orla Thank you for using our product Lisa! @stcohen112 if you are ever interested in reviewing our product, please DM us. dna.sequencing.com/ehlers-danlos-…

Many people asking recently "why is an #hEDS diagnosis important if there's nothing I can do about it?" There's a simple answer and a complex one. Simply: because that's not TRUE - there's LOADS we can do about it. A brief 🧵

DNA Myths Debunked instagram.com/reel/Ck55Btdsa…

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-tec…

.@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/please-welcome…

Great article from @royfurchgott. We are waiting for the day when whole genome sequencing can cost $100. nytimes.com/2022/10/12/bus…