Sold by: enGenome
Best-in-class SaaS for Variant Interpretation
Overview
eVai is a CE-IVD certified cloud platform that helps laboratories, clinicians and researchers interpret genomic variants with accuracy and speed. It leverages Artificial Intelligence to automatically classify, prioritize and suggest candidate diagnoses from NGS data.
Awarded as one of the best-performing predictors in the NIH-funded CAGI6 Rare Genome Project, eVai increased diagnostic yield by 12.5%.
It offers detection accuracy above 99% and classification accuracy up to 98%, ranking pathogenic variants in the first positions.
Its unique digenic and oligogenic prediction capability expands interpretation beyond single-gene analysis. The platform is HIPAA and GDPR compliant, CE-IVD, and ISO (13485, 27001, 9001) certified, making genomic interpretation more reliable and efficient.
For a personalized quotation, please contact us to receive a private offer.
Highlights
- Here's why labs choose us: Award winning AI-driven analysis - Pathogenic variants ranked in first positions - Monogenic and Digenic predictions - Intuitive, fast and CE IVD certified
- Applications: Inherited Disorders, Germline - Cancer and Carrier Screening - WGS, WES and Gene Panels - Nuclear and Mitochondrial SNV, Indel and CNVs - Short and Long reads
Details
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Deployed on AWS
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Pricing
Pricing is based on the duration and terms of your contract with the vendor. This entitles you to a specified quantity of use for the contract duration. If you choose not to renew or replace your contract before it ends, access to these entitlements will expire.
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Dimension | Description | Cost/12 months |
|---|---|---|
Price for 1000 targeted samples | Targeted Samples | $58,000.00 |
Dimensions summary
This contract covers one pricing dimension: a bundle of 1000 targeted samples. You commit to a fixed volume of targeted samples processed through the platform. Pricing scales by the number of sample units you purchase rather than by user seats or compute time. A targeted sample refers to a genomic dataset analyzed for variant interpretation. There are no separate tiers or add-ons to choose from; the single unit defines the full scope of your purchase.
Top-of-mind questions for buyers
A targeted sample is one patient's genomic dataset submitted for variant interpretation. The platform accepts inputs like FASTQ or VCF files from whole genome, whole exome, and panel sequencing. Each dataset analyzed counts as one sample against your committed volume of 1000 units.
No. Billing counts each targeted sample as one unit regardless of how many variants it contains. A dataset with thousands of variants still counts as a single sample. Cost scales only with the number of samples processed, not the complexity of each analysis.
Yes. The platform applies a dual-engine approach covering hypothesis-driven diagnoses for rare diseases and hypothesis-free screening for population-scale analysis. Both workflows draw from the same committed pool of 1000 targeted samples. You are not required to split your allowance between the two use cases.
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