9 services found
CENTOGENE N.V. Services
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Genetic Testing Services
Genetic testing is a type of medical test that identifies changes in genes, inherited from our parents, which we then typically pass on to our children. “Mistakes” in our genes (called “pathogenic variants”) can manifest the disease, and genetic tests may be used to confirm the disease ...
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Whole Genome Sequencing Service
Whole genome sequencing (WGS) identifies almost all changes in a patient’s DNA by sequencing both the entire protein coding and the non-coding regions of the ...
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Whole Exome Sequencing Services
Whole Exome Sequencing (WES) is a comprehensive genetic test that identifies changes in a patient's DNA that are causative or related to their medical concerns. By focusing on the entire protein-coding regions of the genome – the exome – WES offers you the coverage you need to diagnose patients rapidly and ...
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Other Services
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Drug Discovery R&D Collaborations
We work with partners to develop new disease models and new biomarkers of disease. We can also use our disease models to identify new drug targets and screen chemical compounds to identify potential new drug candidates. CENTOGENE provides companies with tools to accelerate drug discovery. From population screening studies that elucidate the prevalence of a rare disease to disease modeling, we are your partner in de-risking drug development for rare ...
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Clinical Trial Support Services
We provide a broad range of services to successfully operate clinical trials. We leverage our proprietary Bio/Databank, multiomic platform, extensive physician network and our experts to ensure efficient and effective solutions to drive progress in the rare disease ...
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Genetic Testing
CENTOGENE’s genetic tests offer patients the most advanced testing technology specifically designed to confirm or exclude a diagnosis of almost any known genetic disorder. An accurate and rapid genetic diagnosis can prevent an odyssey of countless unnecessary medical tests. Our renowned medical experts and scientific advisory board ensure that your genetic test results are comprehensively analyzed and translated into a report that will help physicians guide medical care.
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Infertility Testing
If you are struggling to become pregnant then genetic testing can often identify the cause, and help a significant number of couples in their desire to have ...
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Non-Invasive Prenatal Testing
Want to make sure that your baby is growing and developing normally during pregnancy? CentoNIPT® – Safe and accurate prenatal testing – Offers you information about the health and development of your child from as early as the 10th week of pregnancy.* Non-invasive prenatal testing (NIPT) is a new method of testing for common chromosomal abnormalities that can occur in a developing baby. While rare, these chromosome abnormalities can have ...
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Genetic Testing for Newborns
The fastest and most comprehensive genetic testing available for newborns, infants and children less than 24 months old in intensive care. CentoICU – Genetic Testing When Every Moment Counts. Up to one-third of all babies and children admitted to the ICU have a genetic disease. For many patients, early identification can make a difference in their immediate and long-term ...
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Carrier Screening with CentoScreen
Carrier screening can determine if a healthy person carries a genetic disease, identify people at risk of developing a genetic disease, or help assess the risk of a couple passing a genetic disease onto their ...