Genome NGS | Origin26.com

Best-in-class genome sequencing

We offer fast and accurate results using the most advanced consumer DNA testing technologies – Next Generation Sequencing (NGS). NGS allows us to analyze your entire genome in a single sequence and extract valuable and actionable insights. We then put together a comprehensive report combined with expert advice on how to proactively manage your health.

What is genome sequencing?

Whole genome sequencing is a test used to identify genetic variations within your DNA. The purpose of genome sequencing is to obtain vital medical information so that you can take care of yourself in the best possible way.

Whole genome sequencing

The process uses new and advanced technology that allows us to read a complete set of your DNA (or genome) in one go. The genome is your body’s instruction manual – about 99% of the genome is the same in all human beings. There are about 3 million genetic variations within the 1% difference, and that’s what makes you who you are. We analyze these variations using a whole genome sequencing test to reveal your unique genetic makeup.

Using our test, we offer a comprehensive report that provides an in-depth analysis of your biological characteristics. Here we give valuable information about your diet, your metabolism, your state of health, your food intolerances and allergies, your sleeping habits, your body morphology and even your personality.

The Whole Genome Sequencing Report empowers you to make proactive and meaningful changes in your life with actionable insights. From creating an exercise plan to choosing the most effective drugs for your body. With genome sequencing, Dante Labs can help you live a healthier, happier, and more informed life.

BAGO26 genome sequencing

We developed our platform specifically for whole genome sequencing data. This way we can offer you more personalized information, developed on the most comprehensive genomic test that is the whole genome.

We analyze more data, we uncover the intronic regions of DNA and, most importantly, we apply our proprietary BAGO26 platform to provide you with personalized insights and reports.

Genomics can use gene information to:

Identifying genetic disorders
Diagnose rare diseases more quickly (approximately 80% of all rare diseases are of genetic origin).
Predict their likely response to different treatments, so doctors can more precisely tailor treatment to individuals.
Anticipate their risk of developing disease, which can guide prevention strategies.
Classify cancerous tumors to guide treatment choices.

The Genomics Health Futures mission will build on existing research to demonstrate the benefits of genomics and related technologies for patients and the healthcare system. As the use of genomics becomes more widespread, there will be more and more opportunities to adapt and refine disease management. This means that more costly and avoidable diagnostic procedures and treatments will cease.