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CentoCloud® – Your Digital Bioinformatics Solution

Analyze, interpret, and report genomic variants from anywhere in the world via our decentralized SaaS platform.

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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.

The CentoCloud Collaboration Model

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.

Access

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Superior Panel/Assay Design

Validated and driven by CENTOGENE’s medical expertise and intellectual property in clinical diagnostics

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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

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COmprehensive And highly SensitivE

Custom designed panels that include copy number analysis to deliver our customers the best performance and accuracy

Enable

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Workstation Setup & Validation

Support with quality management and accreditation on request

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Ready-To-Use Protocols

Curated based on CENTOGENE’s more than 15 years of diagnostic experience

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Training in NGS Wet Lab

Training programs available at CENTOGENE's Rostock headquarters or on-site at your laboratory

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Competency Testing

Ensure best practice learning through a competency certificate after training and validation

Stream

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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
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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

Conclude

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Comprehensive

Clinical evidence that is comprehensively curated, analyzed and interpreted bymedical experts

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Clear

Clear diagnoses and follow-up recommendations from our board-certified human genetic experts

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Classification

Identified variants are classified following best practice international guidelines (CMGS/ACMG)

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References

Relevant publications are provided to support our conclusions and as follow-up references

Order a Test on Our Online Ordering Portal

CentoPortal® is a user-friendly, online, web-based ordering portal designed to assist you at every step of processing your patients' samples.

Order a test

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Downloads & Resources

CENTOGENE Sample Report CentoCloud® Genome Solo Female Positive Findings

CentoCloud Genome Solo – Sample Report Positive

POSITIVE RESULT

CENTOGENE Sample Report CentoCloud® Genome Solo Female Negative Findings

CentoCloud Genome Solo – Sample Report Negative

NEGATIVE RESULT

CENTOGENE Sample Report CentoCloud® Exome Trio Parent Positive Findings

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

Contact Us

For our US Partners:

+1 (617) 580 - 2102

Mon. – Fri. 7 a.m. – 8 p.m. CEST


Contact Us