Let us help you with your unsolved cases.

Our special offer for academic research

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.

Solve your cases
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What you will get

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.

Solve your cases

Fill out the form and one of our team members will be in touch to discuss eligibility and next steps.

Why do we do this?

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.

Why our variant classification and prioritisation is better

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.

Solve your cases
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