Streamline end-to-end your clinical & NGS analysis with AI and advanced analytics

Problem: Traditional diagnostic processes are time-consuming and inefficient, delaying patient treatment and impacting health outcomes.

Speed

10x

faster for physicians and clinical laboratory professionals to generate pharmacogenomic reports and run comprehensive analysis pipelines without compromising on quality

Problem: Lack of precise genomic insights, which traditionally take months, leads to generalized treatment plans, resulting in suboptimal patient care.

Get insights

1-3 clicks

to diagnostics & better care insights through integrating clinical & NGS data with powerful AI and advanced software automation

Problem: Slow & inefficient processes for variant interpretation and reporting, patient data management and patient care result in significant operational costs & overheads for healthcare providers

Increase ROI

>325% ROI

Streamline NGS analysis, clinical reporting & patient data management & care with powerful AI and advanced software automation, significantly lowering operational costs & maximising ROI

Features for in-depth analysis of NGS test results in healthcare

Genomic data analysis: Using powerful algorithms, the platform scrutinizes patient-specific genomic data to detect significant genetic variants that could inform therapeutic strategies.
Variant filtering and therapy recommendations: By accessing renowned databases such as ClinVar, COSMIC, and others, the module delivers precise therapy recommendations, streamlining the clinical decision-making process.
Pharmacogenomic reporting: Produce individual participant pharmacogenomic reports to guide clinicians for treatment and dosage recommendations.
Automated, configurable reporting: Generate real-time, dynamic clinical reports that adapt to the latest genomic insights, ensuring that all patient data is accurate and up-to-date for authorized personnel.

Genomic data analysis: Using powerful algorithms, the platform scrutinizes patient-specific genomic data to detect significant genetic variants that could inform therapeutic strategies.
Variant filtering and therapy recommendations: By accessing renowned databases such as ClinVar, COSMIC, and others, the module delivers precise therapy recommendations, streamlining the clinical decision-making process.
Pharmacogenomic reporting: Produce individual participant pharmacogenomic reports to guide clinicians for treatment and dosage recommendations.
Automated, configurable reporting: Generate real-time, dynamic clinical reports that adapt to the latest genomic insights, ensuring that all patient data is accurate and up-to-date for authorized personnel.