VariEx™ Analysis bridges the gap between sequencing and patient care. Our AI-powered platform transforms raw NGS data into actionable clinical reports, helping labs, hospitals and genomic researchers deliver faster, more accurate diagnoses. With end-to-end analysis of gene panels, exomes, and genomes, with advanced annotation for SNVs, CNVs, structural variants, and regulatory elements, we simplify compliance while putting control back in the hands of clinicians and researchers. By accelerating discovery and reducing diagnostic odysseys, VariEx™ advances precision medicine for all.
Carrier Screening
Neonatal Screening
Oncology
Hereditary Diseases
Population Genomics
Rare Diseases
Pharmacogenomics
Prenatal Diagnostic Testing
Carrier Screening
Neonatal Screening
Oncology
Hereditary Diseases
Population Genomics
Rare Diseases
Pharmacogenomics
Prenatal Diagnostic Testing
Engineered for universal compatibility, our platform installs effortlessly into diverse laboratory ecosystems, powering everything from cancer genomics to Mendelian disorder analysis.
Our AI algorithms achieve best-in-class sensitivity and specificity for comprehensive variant calling, including complex structural variations.
Transform time-consuming, complex variant interpretation into rapid clinical insights with VariEx™'s automated annotation and evidence-based classification framework.
Speciality Hospitals
Genome Sequencing Labs
Pharma & Biotech companies
Diagnostics Labs
Goverment Agencies
Let’s talk about how PHS and our digital tools can support your patient recruitment, data workflows, and clinical outcomes.