Enhance throughput and diagnostic yield with AION, our CE-IVDR certified, automated genetic variant interpretation platform.
AION allows you to confidently scale your genomic sequencing operations by tackling the interpretation bottleneck.
Fast & Automated
AION provides an exome interpretation in less than 2 minutes. In addition, a comprehensive report and results export are automatically generated.
White-box Approach
We believe that any AI prediction must be verifiable by a human expert. Therefore, AION provides insights into "how" and "why" variants were classified and prioritized.
Accurate Decision Support
Our unique AI-based platform provides accurate and reliable decision-support at 93.1% sensitivity, as clinically validated on data from the Genomics England 100K Genomes Project.
We combine an intuitive design with in-depth reporting to provide outstanding performance.
Upload a FASTQ or VCF file, add family members, and define patient characteristics, like symptoms as HPO terms.
Review the rank of most relevant variants and associated diseases. Our unique white box approach allows you to understand the underlying factors contributing to the classification of a variant as pathogenic or benign.
Download a full report including all relevant information. The report is available as a PDF and a spreadsheet.
Our AI provides a list of causative variants in an auditable and reproducible manner. It learns from new data, but also benefits from expert knowledge: In addition to 30+ data sources, we have modelled a decade of experience in clinical genetics.
Regularly updated knowledge database with more than 100 annotations, including a selection of data from high-throughput functional genomics assays that directly reflect the molecular impact of thousands of selected mutations.
By combining state-of-the-art artificial intelligence with our regularly updated knowledge base, AION outperforms the rule-based ACMG classification by more than 50%.
For people with genetic diseases, getting the right diagnosis at the right time is critical. With AION you can speed up large parts of your variant interpretation, focus on very complex cases and build a sustainable business.
AION automatically identifies likely pathogenic variants in less than 2 minutes.
AION detected variants with 93.1% sensitivity on data from the Genomics England 100K Genomes Project.
AION is based on a vast, regularly updated and extended database containing >100 annotations.
Download our white paper and learn about AION's clinical validation on the Genomics England 100.000 Genomes Project, as well as latest developments in AI and genomics.
*Nostos Genomics regularly produces webinars, white papers, and other types of content that you may find valuable.
You can unsubscribe at any time. For more information view our Privacy Policy.
AION is easy to use and doesn’t require any integration.
AION's architecture and procedures are designed to provide the highest standards of security and privacy.
Contact us!
*Nostos Genomics regularly produces webinars, white papers, and other types of content that you may find valuable.
You can unsubscribe at any time. For more information view our Privacy Policy.
