eVai platform uniquely combines the ACMG guidelines for variant interpretation with artificial intelligence
Every type of variant in your VCF files is automatically pre-classified according to ACMG guidelines recommendations and scored according to its pathogenic and benign supporting evidences.
Customize variant interpretation by adjusting ACMG pre-classification and criteria, add new supporting evidences and publications: eVai will automatically track and re-use your data to improve variant prioritization over time.
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On top of the benefits of our SaaS platform, we provide complete support for technical issues and product training. Contact us for personalized features, we enjoy such challenges.
Scientific publications and White papers confirm our constant strive to transfer research findings into professional software products.
Since 2011 our scientific team has been developing different bionformatics workflows (DNA-Seq, RNA-Seq, Liquid Biopsy) for customers worldwide.