UGenome: software to make genomic medicine personal
Tools of Genomic Medicine
Grounded in our product philosophy and values, we have a personalized reference genome generating mutation analyzer (MAXX) and pharmacogenomics data extracting analyzer (ProPEx) to help you get a personalized treatment today, not 20 years from now.
MAXX Product Features
MAXX transforms personalized genomics research by shifting from standardized reference genomes (hg19 or hg38) to a Personalized Reference Genome. With enhanced accuracy and specificity in mutant gene expression alignment, it enables more precise detection of genetic variations and minimizes off-target effects, ensuring reliable outcomes with reduced unintended consequences and unmatched precision.
Personalized Genomics
Move beyond standardized reference genomes with MAXX’s ability to generate personalized reference genomes, tailored to each sample, ensuring more accurate analysis.
Comprehensive DNA & RNA Analysis
Conduct both DNA and RNA analysis seamlessly, providing deeper insights into somatic mutations, gene expression patterns, and biological relevance.
Unparalleled Accuracy & Specificity
Enhance mutant gene expression alignment with precision, minimizing off-target effects and reducing unintended consequences, resulting in reliable research outcomes.
Integrated Workflow
MAXX offers a streamlined workflow from personalized reference genome generation to variant calling, annotation, filtering, and report generation, reducing manual effort and complexity.
ProPEx Product Features
Unlock the potential of pharmacogenomics (PGx) with ProPEx. By seamlessly integrating into your existing WGS/WES workflow, ProPEx enables you to extract valuable PGx data without the need for additional samples or complex test development. Expand your service offerings, enhance revenue, and provide clients with personalized medicine insights
Efficient Pharmacogenomic Data Extraction
ProPEx extracts crucial pharmacogenomic data from existing WGS or WES datasets, enabling genetic testing labs to enhance their service portfolio without additional sample collection.
Robust Report Generation
Generate detailed reports in HTML or JSON formats, with three versions available: a concise phenotype table (one-pager), a short version, and a comprehensive long version, catering to different reporting needs.
Comprehensive Gene Coverage
The system focuses on 11 key genes, including CYP2B6, CYP2C19, and CYP3A5, which impact over 100 medications, ensuring that patients receive tailored drug therapy based on their genetic makeup.
Streamlined Workflow Integration
ProPEx integrates easily into existing laboratory processes, simplifying the workflow from data extraction to reporting and ensuring efficient operations.
