One infant One genome Personalised Answers.

A genetic service created by CBR Genomics to improve children's lives.
One infant One genome Personalised Answers.One infant One genome Personalised Answers.

Know to prevent.

Screening for diseases in children is not new. Every year, thousands of babies are tested to screen between 2 to 35 rare and severe diseases. The earlier the detection, the faster and more suitable the clinical actions.
1 in 10
babies have a paediatric disease-causing mutation.
6 000
rare diseases identified worldwide.
70%
of rare diseases are genetic and have infantile-onset.
"Sequencing DNA newborns thoroughly reveals potentially lifesaving information in both infants and their parents far more commonly than was previously thought", Robert Green, physician-scientist.

Why DNA.files BABY?

All parents want the best for their children. This care starts from the first moment.
Why DNA.files BABY?
Screening for a 10-fold extended disease panel
Children may benefit from a more comprehensive screening - for over 300 diseases - through a simple DNA analysis from saliva.
Clinically actionable diseases
DNA.files BABY provides solutions. All screened diseases have a clinical follow-up to prevent or attenuate their development.
DNA sequencing, an investment for life
DNA is unique and immutable. Once sequenced and stored, it can be reanalysed multiple times whenever clinically needed.

The Power of Genomic Medicine.

Medicine is changing! In the future, medicine will no longer be focused on responding to disease, but rather on preventing it.

Detection
Detection
of disease-causing genetic mutations at early stages, before the first symptoms appear.
Prevention
Prevention
of disease development, with a proactive and timely approach.
Personalisation
Personalisation
of clinical decisions, interventions and treatments. Focus on the individual and how to optimise well-being.
Participation
Participation
and empowerment of individuals by the rigor of genetic information, becoming them better prepared to make decisions about their health management.
At CBR Genomics, we put Genetics at the service of Medicine to improve healthcare.

At CBR Genomics, we put Genetics at the service of Medicine to improve healthcare.

Visit CBR Genomics website

Our drivers

Improving people's quality of life based on DNA information.
We feel the urgency of putting the latest scientific advances at the service of health, with a positive impact on people and physicians' lives.

Humanisation
Humanisation
The patient is at the base of all our actions. We develop genetic services to improve people's lives.
Clinical Support
Clinical Support
Our Molecular and Clinical Genetics team provides clinical support to patients and their physicians.
Rigor & Up-to-dateness
Rigor & Up-to-dateness
We bridge the gap between the most advanced and up-to-date knowledge in Genetics and the clinical practice.
Security & Privacy
Security & Privacy
We prioritise data security and privacy at all stages of the service.

Because your baby’s healthcare starts from the first moment.