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eVai platform uniquely combines the ACMG guidelines for variant interpretation with artificial intelligence

Variant Prioritization

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.

Evidence curation

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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Customer Support

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 Proofs

Scientific publications and White papers confirm our constant strive to transfer research findings into professional software products.

Bioinformatics Services

Since 2011 our scientific team has been developing different bionformatics workflows (DNA-Seq, RNA-Seq, Liquid Biopsy) for customers worldwide.

enGenome is an academic spin-off born from the Laboratory of Bioinformatics and Synthetic Biology of the University of Pavia. The company was founded by a team of biomedical engineers expert in bioinformatics, biostatistics and artificial intelligence, working on NGS data analysis for hospitals and pharmaceutical companies since 2009.

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We are looking for collaborations in research projects as in validation of new NGS applications for clinical routine. Contact us for a free consultation.

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