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Exhaustive clinical information at a moderate price

Targeting genes associated with all known clinical phenotypes - Get high diagnostic accuracy with the fastest workflow

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  1. Clinical exome sequencing

Clinical exome sequencing

CentoDx® is our largest NGS panel available, covering over 3,200 diseases in the shortest turnaround time.

CentoDx® focuses on the coding part of all genes associated with known clinical phenotypes, thereby comprising the complete clinical exome. It reduces additional costs and prevents unclear results from sequencing genic regions not related to human diseases.


Why choose CentoDx®?


Covers ~6,700 clinically relevant genes with known associated phenotypes

Needs only 1 μg of DNA

Turnaround time of <30 business days

Sanger confirmation and comprehensive clinical report *

Highlights of CentoDx®

CentoDx® is a clinical exome product that includes ~6,700 clinically relevant genes with known associated clinical phenotypes. This screening method uses boosted probes over these specific genes, which provides a more uniform and robust coverage and performance over genes of clinical interest as compared to whole exome sequencing. Around 4,000 genes within this panel have ~100% coverage in coding regions.

CentoDx® focuses on genes listed in OMIM and HGMD where a clear genotype phenotype correlation has been previously demonstrated.

High diagnostic accuracy with the fastest workflow

Why should you choose CentoDx®?


Downloads for CentoDx®

* Due to our strictest application of quality criteria, we are achieving >99.9% specificity. All reported lower quality single nucleotide variants and all InDels are being confirmed by Sanger sequencing.

Get in touch with our Customer Support

Our consultation service is available in several languages.

+49 (0) 381 - 80113 416

Mon. – Fri. 7 a.m.– 8 p.m. CET • Sat. – Sun. 9 a.m – 5 p.m. CET

For our US customers:

+1 (617) 580-2102

Mon. – Fri. 9 a.m. – 5.30 p.m. EST