CENTOGENE starts HiSeq X® whole genome sequencing (WGS) - first commercial organization in Europe to provide rare disease diagnostic with high-throughput genome analysis
(PresseBox) - 11.2016 - CENTOGENE announces today a new sequencing facility for rare hereditary disorders, which will use Illumina's HiSeq X® sequencer. With its wellestablished high-throughput facility for the early diagnosis of patients with rare diseases, CENTOGENE has reached the global next level of precision and data quality with the application of the whole genome sequencing (WGS) platform HiSeq X®.
CENTOGENE will be the first European company to use the groundbreaking nextgeneration sequencing (NGS) technology for the future generation of patient's genomes in-house validated for diagnostic environment. With this step, CENTOGENE further solidifies its global position as one of the top medical institutions for the early and reliable diagnosis of rare hereditary disorders. The HiSeq X® system performs whole genome sequencing, producing industry-leading data at the most cost efficient way available in the market today. CENTOGENE also successfully became part of the Illumina Propel Certification Program for Core and Service Labs, certified for the HiSeq 4000, the MiSeq® and the NextSeq® technology, which defines a unique standard worldwide and proves the deep knowledge our scientific and medical experts developed and apply in the analytical testing processes.
"When you commit to clinical diagnostics, results have to be fast and reliable. Only this enables the patient and attending physician to choose the best option for personalized treatment. The production of the most complete sequencing data, followed by a proven bioinformatics pipeline, forms the basis for a solid medical interpretation. CENTOGENE's worldwide databank, CentoMD®, together with the HiSeq X® platform will bring the highest level of quality to our patients. Clinical information and validated results will be available when they are needed. Especially the progress in intellectual disability, ultra-rare hereditary diseases, and oncogenetic diagnostics will drive the tremendous progress in whole genome sequencing," stated Arndt Rolfs, CEO at CENTOGENE.
"The adoption of the HiSeq X® system has exceeded our expectations and we are excited that CENTOGENE can take its research to new heights," said Paula Dowdy, Senior Vice President and General Manager, Illumina, Europe, Middle East, and Africa.
"With its high throughput industry leading data, and unprecedented price point per genome, the HiSeq X® system will provide CENTOGENE with an opportunity to help in its efforts to improve human health."
The combination of NGS technology, used at its frontline level, with CentoMD®, the world's largest genomic database for rare genetic diseases, gives the highest credibility to the patients and the medical experts to get a fast and comprehensive interpretation of the complex WGS data. Furthermore, the optimized processes reduce sample process times of ~30%, which result in turnaround times of less than 20 days for the complete lab analysis. The investment in the new high-end WGS technology will further increase the quality and the throughput at CENTOGENE.
CENTOGENE is a worldwide leader in the field of genetic diagnostics for rare hereditary diseases - with the largest test portfolio worldwide. Testing samples from over 100 different countries allows CENTOGENE a unique insight into epidemiological basis of hereditary disorders, which is crucial in the medical result interpretation process. The company is strictly focusing on offering quality molecular genetic diagnostics, underlined by its multiple international accreditations (ISO, CAP, CLIA). CENTOGENE's in depth medical expertise is supported by the application of cutting-edge technologies including next generation sequencing, whole exome sequencing (CentoXome®), whole genome sequencing (CentoGenome®) and innovative biomarkers for selected diseases. CENTOGENE has developed a comprehensive mutation database (CentoMD®) that is pivotal to offering high quality diagnostic reporting and medical interpretation; thoroughly interpret each patient's sequence data. In addition to diagnostic services for individual patients, CENTOGENE is also a pivotal partner for multiple renowned industrials worldwide. CENTOGENE has affiliations in Germany, India, Canada, Austria, and the United Arab Emirates.
For more information, please visit www.centogene.com and info.centomd.com
CENTOGENE is a worldwide leader in the field of genetic diagnostics for rare hereditary diseases - with the largest test portfolio worldwide. Testing samples from over 100 different countries allows CENTOGENE a unique insight into epidemiological basis of hereditary disorders, which is crucial in the medical result interpretation process. The company is strictly focusing on offering quality molecular genetic diagnostics, underlined by its multiple international accreditations (ISO, CAP, CLIA). CENTOGENE's in depth medical expertise is supported by the application of cutting-edge technologies including next generation sequencing, whole exome sequencing (CentoXome®), whole genome sequencing (CentoGenome®) and innovative biomarkers for selected diseases. CENTOGENE has developed a comprehensive mutation database (CentoMD®) that is pivotal to offering high quality diagnostic reporting and medical interpretation; thoroughly interpret each patient's sequence data. In addition to diagnostic services for individual patients, CENTOGENE is also a pivotal partner for multiple renowned industrials worldwide. CENTOGENE has affiliations in Germany, India, Canada, Austria, and the United Arab Emirates.
For more information, please visit www.centogene.com and info.centomd.com
Datum: 28.11.2016 - 12:45 Uhr
Sprache: Deutsch
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