We know most hospitals and academic labs have many unsolved cases in their backlog. Our research offering can help you. Let our clinical geneticists process 100 of your cases on our CE-IVD certified, GDPR-compliant platform. Free of charge.
100 cases processed
Solve previously unsolved cases and uncover new genetic variant disease relationships with the help of our team of experts.
Detailed results
Our whitebox approach lets you understand relevant variants quicker through HPO-driven prioritization.
Increased diagnostic yield
We have done validation studies that confirm higher diagnostic yield with our classification & ranking.
Fill out the form and one of our team members will be in touch to discuss eligibility and next steps.
*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.
We know most hospitals and academic labs have many unsolved cases in their backlog. This is because the interpretation of WES or WGS can be extremely complicated and lengthy. Our CE-IVD-certified platform AION can help you speed up large parts of your variant interpretation and focus on your most complex cases.
We believe that our AI-based platform can greatly support the identification of causative variants when verified by highly skilled human experts. When we process your cases, you will be provided with detailed results for each case. This will enable you to understand the underlying reasons that form the basis of our variant classification and prioritisation.
Our mission is to support people with genetic disorders to get a fast and clear diagnosis. Based on our internal and external validation, the quality of our results should benefit more people. By collaborating with outstanding academic research institutions, we believe that we can have a positive, tangible impact on those people.
Molecular variant effect prediction
Predicted molecular effects for >100M variants across all human genes including functional effects on RNA and protein, and essential genomic regions.
Clinical variant effect prediction
Genotype-phenotype associations for >4000 human diseases, including clinical symptoms and laboratory and imaging test alterations.
Rich data sets complemented by expert knowledge
Insights generated by expert in-house analysis of genetic and clinical data from >50K rare disease patients.
