The following is a review of Nebula Genomics's Initial Coin Offering of the "N/A" token. Get information about the Nebula Genomics ICO including; start date, end date, financial information, whitepaper, team profile and other important information regarding this new token.

Innitial Coin Offering (ICO) Information

ICO NameNebula Genomics
Start DateTBA
End DateTBA
ICO Time
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The first human genome was sequenced in 2001 at a cost of $3 billion. Today, human genome sequencing costs less than $1000, and in a few years the price will drop below $100. Thus, personal genome sequencing will soon be widely adopted as it enables better diagnosis, disease prevention, and personalized therapies. Furthermore, if genomic data is shared with researchers, the causes of many diseases will be identified and new drugs developed. These opportunities are creating a genomic data market worth billions of dollars.

Do you have canker sores? Your genetics could be responsible. A new study has identified 97 genetic factors that influence canker sore risk. Based on these factors, existing drugs for psoriasis and Crohn's might be repurposed to treat the condition.

The first genetic defect linked to the liver disease biliary atresia has been found by using genetic data gathered over 15 years. Allowing people to privately, securely, and equitably share their data with researchers will facilitate discoveries like this.

@jacksondahl Not a huge a16z podcast guy but holy crap this one with @geochurch on the state of genetics tech and ethics is nuts:

You should decide who hears your story. You should also decide what happens to your genetic data. You can choose to (or not to) share it with those researching #raredisease. @TheMightySite & @NebulaGenomics are doing a sequencing #giveaway. Learn more:

Contribute to medical breakthroughs and receive a clinical grade whole genome sequencing report for free-- @NebulaGenomics and @RareAdvocacy are giving away 5 free tests to patients for their feedback. Enter the #giveaway here: #raredisease #rarediseaseday

RAM has decided to take @NebulaGenomics up on their offer! 5 genome sequencing tests will be awarded at random via a giveaway. ‚ÄčA report summarizing the patient's experiences will be published upon completion. Learn more at #RareDiseaseDay #rareadvocacy

Sharing your story with the world can show others with #rarediseases they're not alone. Be the voice you needed to hear after your diagnosis and share your story with @TheMightySite here: #worldrarediseaseday #rarediseaseday #rarediseaseday2019 #WRDD2019

Did you know that 1 in 10 people are affected by a #raredisease? Get the facts at @GlobalGenes #worldrarediseaseday #rarediseaseday #rarediseaseday2019 #wrdd2019

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PriceN/ASaleN/APayment ModeETH
Minimum InvestmentN/ADistributionN/ARaisedN/A
Soft CapN/AHard CapN/A

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