MedySapiens | MedyCVi®

Solutions

MedyCVi®

MedySapiens' Cloud for Variant interpretation

What is
MedyCVi®?

MedyCVi® is

A system capable of analyzing genetic mutations for rare disease diagnosis based on artificial intelligence.

Regularly updated with newly discovered genetic variations by MedySapiens, in addition to major genome databases.

MedyCVi® also provides sophisticated analysis to support medical professionals' diagnoses faster and more accurately through the NEOseq_ACTION® panel for NICU (Neonatal Intensive Care Unit) and NGS sequencing technology

Who is
MedyCVi®for?

MedyCVi® is

A cloud solution provided to global hospitals, enabling medical professionals worldwide to easily analyze genetic mutations without specialized expertise through customized bioinformatics pipelines.

MedyCVi® provides user convenience by offering approximately 20 databases, including several clinical DBs, population frequency DBs, and protein structural change prediction DBs, to evaluate genetic information and mutation pathogenicity.

Why is
MedyCVi®necessary?

Rare diseases reported worldwide exceed 7,000, and most rare disease patients do not receive appropriate treatment and management due to diagnostic difficulties.

MedyCVi® aids in rare disease diagnosis through excellent mutation interpretation, enabling more focus on treatment and management.