CentoCloud® – Your Digital Bioinformatics Solution
Analyze, interpret, and report genomic variants from anywhere in the world via our decentralized SaaS platform.
What Is CentoCloud?
CentoCloud is a cloud-based Software as a Service (SaaS) platform specifically designed for human genetic laboratories to support the execution of high-standard Next Generation Sequencing (NGS) based diagnostics. The fully automated bioinformatics pipeline analyzes NGS data based on CENTOGENE's validated testing products, annotated with data from our proprietary rare disease-centric Bio/Databank.
Why Choose CENTOGENE?
Rare disease-centric Bio/Databank with over 600,000 patients
International team of genetic and bioinformatics experts
Advanced logistical solutions, from sample sending to report administration
Short turnaround time and timely medical reporting
With CentoCloud, we enable laboratories around the world to establish and run state-of-the-art genomic testing and deliver best diagnostic insights to local patients.
The CentoCloud Collaboration Model
Our services include the transfer of our expert knowledge and protocols to those just starting out with NGS operations, clinical bioinformatics, and variant annotation from FASTQ files, all the way to medical interpretation and reporting.
Superior Panel/Assay Design
Validated and driven by CENTOGENE’s medical expertise and intellectual property in clinical diagnostics
Unique Variant Coverage
Based on proprietary variants from the world’s largest diversity of rare disease patient cohorts and public databases
Best Diagnostic Reliability
End-to-end validated gene panels containing fully curated variants that comply with highest standards of CAP/CLIA requirements
COmprehensive And highly SensitivE
Custom designed panels that include copy number analysis to deliver our customers the best performance and accuracy
Workstation Setup & Validation
Support with quality management and accreditation on request
Ready-To-Use Protocols
Curated based on CENTOGENE’s more than 15 years of diagnostic experience
Training in NGS Wet Lab
Training programs available at CENTOGENE's Rostock headquarters or on-site at your laboratory
Competency Testing
Ensure best practice learning through a competency certificate after training and validation
Fully-Automated Bioinformatics Solution
A highly automated bioinformatics pipeline to accelerate diagnostic timelines
- Accepts raw sequencing data from Illumina sequencing technology in FASTQ format
- Alignment to genomic reference sequence
- Variant calling, copy number analysis, and annotation with public databases
Bio/Databank Annotation
Provide filtered variant list with annotations from our proprietary Bio/Databank
- >600,000 analyzed rare disease cases; >120 countries worldwide
- >3,500 associated phenotypes; 14,000 HPO terms; and >600,000 individuals-HPO associations
- >31,000,000 unique variants with HPO related phenotypes; 59% unpublished
Comprehensive
Clinical evidence that is comprehensively curated, analyzed and interpreted bymedical experts
Clear
Clear diagnoses and follow-up recommendations from our board-certified human genetic experts
Classification
Identified variants are classified following best practice international guidelines (CMGS/ACMG)
References
Relevant publications are provided to support our conclusions and as follow-up references
Downloads & Resources
CentoCloud Exome Trio – Sample Report Positive
CARRIER STATUS CONFIRMED – Likely pathogenic variant identified
Contact Us To Find Out More About CentoCloud!
Our consultation service is available in several languages.
+49 (0) 381 - 80113 416
Mon. – Fri. 7 a.m. – 8 p.m. CEST
Sat. 8 a.m. – 12 p.m. CEST