Our Tests

A drop of blood can change your patient’s life. Support your patients fully with accurate information and helpful advice.

Products & Services: Reveal the Cause of Genetic Diseases

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 Key Products

NGS Panels

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.

Multiomic Solutions

Join our multiomics revolution – a multidimensional approach looking at each patient from different angles to combine deep knowledge and insights for a holistic view.

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Newborn Testing

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.

Mitochondrial Disease Testing

CentoMito^® helps to identify mitochondrial diseases to determine possible treatments and to suggest the best fitting therapy.

Reproductive Testing

Prenatal Testing

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.

Carrier Screening

CentoScreen^® is our carrier testing option that helps to asses if a healthy person is a carrier of a recessive genetic disease and. CentoScreencan help partners make informed decisions and choices regarding family planning.

Non-Invasive Prenatal Testing

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.

Additional Products

CENTOGENE Father and Son Playing Baseball

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.

CENTOGENE Father with small Child in Field

Metabolic Testing

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.

We are dedicated to providing the complete spectrum of genetic, biochemical, and biomarker analyses.

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.

Visit our online ordering portal CentoPortal

Get in Touch With Our Customer Support

Our consultation service is available in several languages.

+49 (0) 381 80 113 - 416

Mon. – Fri. 7 a.m. – 8 p.m. CEST 
Sat. 8 a.m. – 12 p.m. CEST

For our US Partners:

+1 (617) 580 - 2102

Mon. – Fri. 9 a.m. – 5:30 p.m. EST 