The impact on human lives of genetic tools can be crucial and Dante Labs wants to democratize genetic information. It aims to break the rules of this very expensive and long-standing sector, giving people the chance to consciously prevent themselves and take care of their health.

Therefore, Dante Labs has become the first company in Europe to make genome tests accessible for any single person with a price lower than $1.000 and the second in the whole world.

In April 2017, Dante Labs started offering the WGS for $900 and in its first year of life, Dante Labs served over 90 countries around the world, reaching with its logistics service from the largest metropolises to the smallest island in the middle of the Pacific.

Genome Sequencing

The core business of Dante Labs is Genome Sequencing, a method for analyzing human genomes in DNA. It has been instrumental in identifying inherited disorders, characterizing the mutations that drive cancer progression, and tracking disease outbreaks.

We build genomic applications based on this data, revolutionizing standard care. Our applications provide people and healthcare professionals with tools and reports to extend and improve their lives with unparalleled precision and accuracy for unbiased exploration of the human genome.

You can consult your DNA in case of pathologies, but it also helps to implement a personalized lifestyle on prevention, nutrition, fitness, and appropriate and personalized use of drugs.

We do it powered by a

Next Generation Sequencing Technology

  • Technologies

    Next Generation Sequencing (NGS) is a series of technologies that allow large genomes sequencing in a short time. It is used to identify the order of nucleotides in genomes or targeted regions of RNA or DNA. 

    These technologies have achieved several goals such as workflow optimization, result customization, data analysis, and interpretation with an ultra-high throughput, scalability, and speed.

  • Precision Medicine

    NGS is supported by Precision Medicine, a revolutionary approach for disease treatment and prevention that takes into account the variability of proteins or genes of each individual to prevent, diagnose, or treat disease.

    Researchers and doctors, considering clinical and lifestyle information, are now able to predict more precise treatments and strategies to cure specific health issues, reducing the treatment time.

It is also called Personalized Medicine

and put beside our NGS and WGS, it will improve our quality of life through our four Genome tests: