We utilize advanced genomic sequencing technologies and sophisticated bioinformatics tools to analyze genetic data and identify potential variants associated with rare diseases and oncology. Learn More

Technology
Our Octopus Owie™ Platform is a comprehensive and user-friendly solution for analyzing genetic variations in cancer, rare diseases, and preventive genomics.
Features
Octopus Owie™ covers a wide range of genetic variants, including single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), and structural variations (SVs).


Services
At Genexfy, we specialize in comprehensive genomic analysis and data-driven solutions, with a particular focus on rare diseases, oncology, and their association with genes.