A drop of blood can change your patient’s life. Support your patients fully with accurate information and helpful advice.
A definitive diagnosis can bring great relief to patients and families, especially when they have been searching for answers a long time. Our solutions go much beyond laboratory testing and medical interpretation – leveraging our Bio/Databank, our global clinical network and deep medical expertise, and our proprietary CentoCard®-based sample logistics.
Our goal is to rapidly diagnose rare, metabolic, and neurodegenerative diseases at the earliest possible moment. We turn data and insights from our database intelligence into actionable results for physicians, patients, and pharmaceutical partners.
Our solutions go far beyond laboratory testing and medical interpretation. They leverage our Bio/Databank, our global clinical network and deep medical expertise, and our proprietary CentoCard-based sample logistics. Our state-of-the-art genetic and multiomic testing are at the core of what we do.
Why Choose CENTOGENE?
Distinctive product offering centered around high-quality genetic testing
Strong presence in and access to countries with a high prevalence of rare diseases
CentoCard provides easy logistics for central testing
Rare disease-centric Bio/Databank generates best-in-class medical insights
Deep expertise in rare, metabolic, and neurodegenerative diseases, as well as multiomics enables better diagnostics
Our NGS panels test for an array of genetic conditions, both hereditary and non-hereditary. They offer a fast, thorough, and cost-effective diagnostic tool for patients with distinctive clinical features or those who are at risk of developing a genetic disease.
Whole Exome Sequencing
CentoXome® can turn years of searching for a diagnosis into days – powered by our best-in-class insights, superior technology, extensive clinical experience, and wealth of rare disease genetic data.
Whole Genome Sequencing
WGS is a comprehensive view of patients’ DNA. CentoGenome® is the most complete solution to diagnose genetically complex and undiagnosed cases with the highest level of certainty.
Remote Diagnostics with CentoCloud®
CentoCloud supports remote, high-standard, next generation sequencing diagnostics. Our bioinformatics pipeline, annotated with data from our proprietary database, analyzes DNA sequence generated by labs around the world.
Join our multiomics revolution – a multidimensional approach looking at each patient from different angles to combine deep knowledge and insights for a holistic view.
CentoICU® is designed to diagnose genetic conditions that become present in the newborn or early childhood period. Many of these have overlapping phenotypes and diagnosis may have immediate implications for the treatment of newborns and children.
Hereditary Cancer Testing
Our medical and genetic experts can help determine which genetic testing is right to analyze if your patient has an increased risk for hereditary cancer.
Somatic Cancer Testing
Somatic mutation testing is of enormous help for survival and life-quality of cancer-affected patients and their families. Discover our oncogenetic panels and detect the most common cancer causing mutations.
Prenatal testing identifies disease-causing mutations in at-risk couples or pregnancies before birth and is offered for congenital or early-onset diseases. Prenatal testing is given the highest priority at CENTOGENE.
CentoScreen® is our carrier testing option that helps to asses if a healthy person is a carrier of a recessive genetic disease and. CentoScreen can help partners make informed decisions and choices regarding family planning.
CentoNIPT® is a non-invasive prenatal test that screens for the most common fetal chromosomal abnormalities, combining the latest next generation sequencing technology with expert medical reporting.
Single Gene Testing
Many genetic diseases are known to be caused by changes or variants in a single gene. At CENTOGENE, we provide the most comprehensive range of diagnostic tests for a broad spectrum of single-gene disorders.
CentoMetabolic MOx – a panel that integrates genetic and biochemical testing for a fast diagnosis of a wide range of rare metabolic diseases.
Chromosomal Microarray Testing
CentoArray® – our chromosomal microarray analysis solution – enables genome-wide detection of large copy number variations and of large blocks of homozygosity, which may represent uniparental disomy.
Our commitment is to convert diagnostic data rapidly into the best solution for each individual patient. With the highest quality in medical interpretation, our extensive rare disease-centric Bio/Databank, and global data sources, we continuously develop new and innovative diagnostic products. Combined with our online ordering platform CentoPortal® and convenient sample collection solution CentoCard®, we offer a comprehensive and convenient testing service.