Analysis & Bioinformatics Infrastructure
Clinical-Grade Genetic Analysis Platform
Advanced variant filtering and AI-powered interpretation for WES, WGS, and polygenic risk assessment—built for Middle Eastern populations.
From Genetic Data to Clinical Insights
Advanced variant filtering and AI-powered interpretation for clinical and polygenic genetics
Raw Genetic Data
WES, WGS, and Microarray inputs
AI-Powered Filtering
Advanced variant analysis
Clinical-Grade Insights
Actionable genetic reports
Genetic testing generates millions of variants, but only a small fraction are clinically relevant. Our platform uses advanced filtering algorithms and AI-powered analysis to identify pathogenic and likely pathogenic variants with clinical-grade accuracy.
Our platform handles both clinical genetics (WES and WGS for rare disease diagnosis) and polygenic risk assessment (microarray-based analysis for common disease predisposition). The unified interface allows geneticists to analyze, interpret, and generate clinical reports efficiently.
Comprehensive Genetic Analysis Suite
Advanced filtering, AI-powered interpretation, and population-specific insights
Advanced Variant Filtering
Powerful filtering platform that processes millions of variants from WES and WGS data, applying clinical guidelines (ACMG), population frequency, and pathogenicity predictions to identify clinically relevant mutations.
- •Multi-criteria filtering (gene, frequency, pathogenicity, inheritance)
- •ACMG/AMP classification standards
- •Support for VCF, BAM, and FASTQ formats
- •Real-time filtering with instant results
Clinical-Grade Interpretation
AI-powered interpretation engine that provides evidence-based clinical insights for each variant, including disease associations, inheritance patterns, and treatment implications following international guidelines.
- •Automated variant classification (Pathogenic, Likely Pathogenic, VUS, Benign)
- •Disease-gene association databases (OMIM, ClinVar, HGMD)
- •Clinical report generation with evidence summary
- •Genetic counselor review workflow
Population-Specific Database
Curated database of 120K+ people from Middle Eastern populations, improving diagnostic accuracy by providing relevant allele frequencies and population-specific pathogenicity data.
- •120,000+ Middle Eastern people
- •Population-specific allele frequencies
- •Reduced false positives in regional populations
- •Continuously updated with local data
Clinical & Polygenic Analysis
Unified platform for both rare disease diagnostics (WES/WGS) and common disease risk assessment (polygenic scores from microarray data), providing comprehensive genetic insights.
- •WES (Whole Exome Sequencing) analysis
- •WGS (Whole Genome Sequencing) analysis
- •Microarray-based polygenic risk scores
- •Combined clinical and risk reports
AI-Powered Insights via CDSS
Genetic analysis seamlessly integrates with our Clinical Decision Support System, where AI combines genetic data with clinical records for comprehensive patient risk stratification and treatment recommendations.
- •Automated risk prediction algorithms
- •Integration with clinical data
- •Personalized treatment recommendations
- •Continuous learning from new genetic evidence
Clinical-Grade Quality & Security
Built for clinical diagnostics with quality control pipelines, audit trails, and healthcare-grade security to meet regulatory requirements for genetic testing labs.
- •CAP/CLIA-compliant workflows
- •Complete audit trails for regulatory compliance
- •Secure genetic data storage (HIPAA-ready)
- •Quality control and validation checks
Built For Genetic Testing Professionals
From clinical diagnostics to population research across the GCC region
Clinical Genetic Testing Labs
Streamline your clinical genetic testing workflow with advanced filtering, automated interpretation, and compliant reporting for rare disease diagnostics and carrier screening.
Use Cases
- •Rare disease diagnostics (WES/WGS)
- •Carrier screening programs
- •Pharmacogenomic testing
- •Hereditary cancer panels
Clinical Geneticists & Counselors
Evidence-based variant interpretation with comprehensive disease databases and clinical guidelines integration to support accurate diagnosis and genetic counseling.
Use Cases
- •Clinical variant interpretation
- •Patient report generation
- •Family cascade screening
- •Genetic counseling support
Genomics Research Institutions
Population-specific genetic research with curated Middle Eastern variant databases, enabling discovery of novel disease associations and improved diagnostic tools for regional populations.
Use Cases
- •Population genomics studies
- •Disease gene discovery
- •Variant database curation
- •Clinical research trials
Seamless Data Import & Integration
Support for all standard genetic data formats with direct integration to Clinical Decision Support
Integration with Clinical Decision Support
Genetic insights automatically feed into our Clinical Decision Support System, where AI combines genetic data with clinical records for comprehensive patient risk assessment.
Learn about Clinical Decision SupportIntegration Workflow Highlights
Core 1 outputs synchronize with Core 2 so clinicians receive contextualized insights without leaving their workflow.
Core 1: Genetic Analysis
Core 2: Clinical Decision Support
Comprehensive Health Intelligence
AI combines genetic insights with clinical data to provide actionable patient risk assessment and personalized treatment recommendations
Accelerating Genetic Diagnosis
Measurable outcomes for genetic testing labs and clinical genetics teams
Advanced filtering reduces variant analysis time from hours to minutes, accelerating time-to-diagnosis for patients with rare diseases.
Population-specific allele frequencies from our 120K+ Middle Eastern database significantly reduce false positive findings.
Clinical-grade interpretation following ACMG guidelines with complete audit trails and quality control for regulatory compliance.
Additional Benefits
Clinical-Grade Security & Compliance
Built to meet genetic testing lab regulatory requirements and protect sensitive genetic data
Data Security
- •End-to-end encryption
- •Secure genetic data storage
- •Access control (RBAC)
- •Audit trails for all actions
Lab Compliance
- •CAP/CLIA-compliant workflows
- •Quality control pipelines
- •Validation documentation
- •ISO 15189 ready
Healthcare Standards
- •HIPAA-ready architecture
- •GDPR compliant
- •GCC data residency options
- •Genetic privacy protection
Quality Assurance
- •Automated QC checks
- •Variant validation protocols
- •Inter-laboratory comparison
- •Proficiency testing support
Compliance Standards
*Built to support lab certification processes
Explore Our Genetic Analysis Reports
See how our platform generates clinical-grade genetic reports with population-specific insights for Middle Eastern populations.
Frequently Asked Questions
Common questions about our genetic analysis platform
Ready to Enhance Your Genetic Testing Capabilities?
See how our platform can streamline your genetic analysis workflow and improve diagnostic accuracy.
Trusted by genetic testing labs across the GCC region • 120K+ people in database