Sequencing

Use your DNA to live healthier, happier and longer. Order DNA tests & get your whole genome sequenced. Free DNA reports for 23andMe, Ancestry, MyHeritage & more

[Sequencing @SequencingCom]

Get offer: https://t.co/VLHxba7C6G

[Sequencing @SequencingCom]

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.

[Sequencing @SequencingCom]

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.

[Sequencing @SequencingCom]

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.

[Sequencing @SequencingCom]

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.

[Sequencing @SequencingCom]

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

[Sequencing @SequencingCom]

"Globally https://t.co/apwA4sQpee’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."

https://t.co/bVsrRCYYFz

[Sequencing @SequencingCom]

Genome Sequencing Appears to Edge Out Exome Sequencing in Clinical Utility in Meta-Analysis.

https://t.co/m6IFtbkaK7

[Sequencing @SequencingCom]

@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

[MediFind @medifindhealth]

Everyone deserves access to the best healthcare possible. That’s why we’ve teamed up with @SequencingCom to provide exclusive access to cutting-edge whole genome sequencing (100% of your DNA). Get screened today and make more informed health decisions. https://t.co/0GBnqEtXpx

[UNDIAGNOSED @UndiagnosedFilm]

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

[Sequencing @SequencingCom]

Within a few weeks of the public announcement from NBCI, the https://t.co/apwA4sQX3M 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 @SequencingCom]

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

[Sequencing @SequencingCom]

@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.

[Rare Disease Day @rarediseaseday]

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!

[Sequencing @SequencingCom]

"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. "

https://t.co/ug0ubCM4Js

[NCATS @ncats_nih_gov]

Register today for #RareDiseaseDay at @NIH and join NCATS, @DRDRI_NCATS and the @NIHClinicalCntr to learn more about #RareDiseases research on Feb. 28: https://t.co/Gy0hn0UsuP 1/2 #RDDNIH

[Sequencing @SequencingCom]

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?

[Sequencing @SequencingCom]

@LisaHandwovens @stcohen112 @hola_orla Thank you for using our product Lisa!

@stcohen112 if you are ever interested in reviewing our product, please DM us. https://t.co/Ki7s1VaveB

[Sequencing @SequencingCom]

DNA Myths Debunked https://t.co/ZQJWhBZ3aG

[Sequencing @SequencingCom]

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
https://t.co/HHJU2INPhz