We support the development of healthcare towards more efficiency, prevention and early detection.
Clinical exome sequencing
Cerba is using clinical exome sequencing since 2016 to search abnormalities in the sequence of a gene. It has become possible thanks to the performance of massive parallel sequencing. It allows non-targeted analysis, at very high resolution, of qualitative modifications of genes. The analysis is performed by comparing the sequence of the patient's exome to reference sequences obtained by sequencing a group of healthy individuals.
The syndromic approach
The syndromic approach is a new way of diagnosing infectious diseases that allows the simultaneous detection of all the most common microorganisms responsible for an infection in a single test. Cerba HealthCare has pioneered this approach by developing tests for all pathogens potentially involved in respiratory, gastrointestinal or sexually transmitted infections.
Find out more
Gut microbiota assessment
Maintaining good health is a major element in the prevention of many diseases and our patients are increasingly aware of this. This observation led us in 2014 to develop a range of functional and preventive biology assessments, including a gut microbiota assessment for hygienic and dietary advice. Since 2019, Cerba, our specialized clinical pathology laboratory has been offering a gut microbiota analysis test that relies on high-throughput sequencing techniques (NGS). A real evolution compared to culture tests, this technique makes it possible to determine the complete mapping of bacterial flora in the intestine.
Find out more
NIPD
In 2013, the French National Authority for Health included in its recommendations the non-invasive prenatal diagnostic test (NIPD) developed by Cerba HealthCare: a genetic test that detects trisomy 21 through DNA circulating in the mother's blood. Rapid and reliable, this genetic test marked a breakthrough in the screening strategy for trisomy 21, since it allowed a diagnosis via a simple blood sample from the mother and without recourse to sampling the amniotic fluid of the foetus, an invasive and lethal procedure for 1% of foetuses. At the end of 2013, Cerba became the first specialized clinical pathology laboratory in France to make its diagnosis test for trisomy 13, 18 and 21 by free circulating DNA available to the medical profession.
Find out more
De Vivo's disease
Rare diseases are also a field of medical investigation that many scientists are involved in. Since 2017, our blood diagnosis for De Vivo's disease has replaced lumbar puncture. Developed in partnership with the start-up Metafora, this non-invasive test is the first in history to benefit from an innovation package (exemption reimbursement). More than 700 child patients have already benefited from it.
Find out more