Benefit from our expertise in Genetic testing
We work with the hundreds of medical experts – meticulously interpreting, reviewing, and approving genetic lab results.
We are a Group of Professionals
We offer the world’s largest genetic testing portfolio with 19,000 genes represented.
We aim to deliver top-notch solutions that are tailored to suit each individual’s unique requirements.
NGS Panels
Our Next Generation Sequencing (NGS) panels test for a range of hereditary and non-hereditary conditions, providing fast and thorough results. Whether your patients have unique clinical features or are at risk of developing a genetic disease, our NGS panels can offer a cost-effective solution for diagnosis.
Whole Exome Sequencing
With our WES you can turn years of searching for a diagnosis into days. Our advanced technology, expert clinical experience, and vast insights into rare and neurodegenerative diseases enable you to deliver rapid and reliable diagnosis.
Whole Genome Sequencing
We use CentoGenome, the world’s most comprehensive Whole Genome Sequencing (WGS) tool for diagnosis of rare and neurodegenerative diseases. This first-line test combines Polymerase Chain Reaction (PCR)-free technology powered by a CE-IVD bioinformatics pipeline and the CENTOGENE Biodatabank to significantly reduce time and resources.
Our services cater to both patients and healthcare professionals seeking accurate and reliable genetic testing solutions.
we understand that a timely and accurate diagnosis is crucial for patients and their families, especially when a long diagnostic odyssey spanning years and multiple misdiagnoses have taken place. That's why we offer a comprehensive diagnostic portfolio that goes beyond standard laboratory testing and medical interpretation in global clinical network, and deep medical expertise as powered by our International Partner Centogene GmbH, Germany.
...everything, anywhere.
Our Services
We offer a wide range of Integrated Genetic 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.
Non-Invasive Prenatal test (NIPT)
Non-invasive prenatal test (NIPT) that screens for the most common fetal chromosomal abnormalities – combining the latest NGS technology with expert medical reporting.
Carrier Screening
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.
Single Genes
Many genetic diseases are caused by changes or variants in a single gene. We offer a comprehensive range of tests for myriad single gene disorders.
Chromosomal Microarray Analysis
Chromosomal microarray analysis (CMA) is recommended for analyzing cytogenic variations in patients suffering for unexplained developmental delays, intellectual disabilities, autism spectrum disorders, and/or multiple congenital malformations.
Metabolic Testing
With a multiomic approach, we can help you and your patients accelerate the critical journey from symptoms to diagnosis by avoiding stepwise testing – saving time, resources, and pivotal years during which Inherited metabolic disorders (IMDs) can rapidly progress.
Our commitment to excellence
Ensure that our clients receive the highest quality services possible.
Uniqueness
Our multidimensional approach enables a complete clinical picture for the most holistic diagnosis, prognosis, and monitoring.
Our Test
Deliver life-changing answers with advanced genetic and multiomic testing, unparalleled data analysis, and a global network of medical experts.
...everything, anywhere.
Are you searching for a simple option to request a diagnostic analysis, we assist you at every step of processing your request.