The JAX Blog

Learn about new technologies and discoveries focused on precise and personalized treatments for patients.


Bridging the gaps in DNA sequencing
Blog Post: Mark Wanner January 10, 2017

Bridging the gaps in DNA sequencing

Even the best short read whole genome sequences aren’t whole. At least five percent of the DNA bases — more than 150,000,000 of them in human genomes — aren’t included in whole genome data. They can also leave out other information that can be vital for disease diagnosis. Why is that?

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