Hey Rare Disease Community! Sign up to our email list to get updates on our service roll out and other important announcements. https://t.co/yPXf20GGRH | #RareDisease#RareButNotForgotten
Watch for the release of our new project "DeepNEU: Stem Cell Suite", coming soon. Validated stem cell disease models will be released to not for profit researchers as they become available beginning in September 2018.
123Genetix is an innovative social enterprise created to empower rare disease research. We have created a growing library of computational models of rare diseases around the globe. https://t.co/yPXf20GGRH
DeepNEU is our big data solution specifically engineered to empower rare disease researchers. Learn more at https://t.co/fjmRcqaRim | #RareDisease#BigData#DeepNEU
To empower rare disease research we have created a growing library of computational models of rare diseases around the globe. These models are easily customizable by the investigator and have a number of important applications. https://t.co/yPXf20GGRH
#Rare disease research is hindered by very limited resources.
We plan on doing something about this.
Learn more at https://t.co/yPXf20GGRH | #RareDisease#RareButNotForgotten
We will be releasing our first validated artificial stem cell simulation of Cystic Fibrosis, free of charge to not for profit researchers later this month. #cysticfibrosis@123Genetix#RareButNotForgotten
Watch for the release of our new project "DeepNEU: Stem Cell Suite", coming soon. Validated stem cell disease models will be released to not for profit researchers as they become available beginning in September 2018.
123Genetix is an innovative social enterprise created to advance rare disease research with our predictive computer modeling technology.
https://t.co/yPXf20GGRH | #RareDisease#RareAction
While there's currently no cure for Rett syndrome, potential treatments are being studied. Our computer simulations could help researchers better understand Rett syndrome. https://t.co/IQb5gwuQAH … … | #RettSyndrome#RareDisease#AI
Do you wish #RareDisease researchers had more tools at their disposal. Do you wish researchers had a better understanding of your (or your kid's) rare disease? https://t.co/lbQuPEItrY
Roughly 30 million North Americans have a #RareDisease. If just 0.1% of that 30 million, yes just 1 out of every 1,000 people with a rare disease, donated $1 to our #HackRare campaign, we would exceed our goal by 50%. https://t.co/jpQxnB4Z7z | #StrongerTogether@RareDiseases
At 123Genetix we believe that rare should not mean forgotten. To empower #RareDisease research we have created a growing library of computational models of rare diseases around the globe. https://t.co/yPXf20GGRH