RgenX-DM is a clinical genomics solution that integrates symptoms with genomics data to identify causative variants, including VUSes and delivers ready-to-use customized reports that accelerate diagnosis.
With a curated dataset of over 900,000 VUS-gene, 300,000 phenotype-disease and 17,000 variants-gene associations, it dramatically reduces turnaround time, making high-end genomics fast, accessible and actionable.
VUSkb is a dynamic database built to resolve the ambiguity of Variants of Uncertain Significance (VUS). A self-updating library of 17068 genes, 8,76,661 variants, 39,030 diseases and 10+ cross-reference databases.
It integrates advanced AI with multi-dimensional biological, clinical, and scientific data, to deeply annotate and prioritize variants. It provides structural, functional, and clinical insights that significantly enhance the interpretation of variant pathogenicity.
VUSkb is a dynamic database built to resolve the ambiguity of Variants of Uncertain Significance (VUS). A self-updating library of 17068 genes, 8,76,661 variants, 39,030 diseases and 10+ cross-reference databases.
It integrates advanced AI with multi-dimensional biological, clinical, and scientific data, to deeply annotate and prioritize variants. It provides structural, functional, and clinical insights that significantly enhance the interpretation of variant pathogenicity.
