GeneAssure Clinical
GeneAssure Clinical is a powerful genomic variant analysis platform for WES, WGS, and targeted panels automating your pipeline from FASTQ to clinical report with AI-powered precision and speed.
The Future of Clinical Variant Analysis
GeneAssure Clinical eliminates bioinformatics bottlenecks, providing a clear path from raw data to comprehensive, actionable reports.
Human Germline Focus
Expertly designed for human DNA, ensuring the highest accuracy for clinical and diagnostic applications.
Multi-Assay Support
Analyze data from WES, WGS, and targeted gene panels within a single, unified platform.
End-to-End Automation
From FASTQ to annotated VCF, our automated pipeline saves valuable time and reduces manual errors.
Rich Annotation
Integrates ClinVar, gnomAD, and other critical databases for comprehensive variant interpretation.
IGV Integration
Visually inspect alignments and variant calls directly within the platform using the built-in IGV.
Insightful Reporting
Generate clear, tangible reports with QC stats, variant tables, and everything needed for clinical assessment.
Your Workflow, Simplified
A simple, four-step process to take you from sample to report with confidence and ease.
Upload Data
Securely upload your FASTQ, BAM, or VCF files directly to our cloud platform.
Configure Analysis
Select your assay type (WES, WGS, Panel) and set analysis parameters with a few clicks.
Review & Filter
Interactively filter variants, review QC metrics, and visualize results in IGV.
Generate Report
Export a comprehensive, lab-ready report with actionable insights.
From Data to Discovery
GeneAssure Clinical transforms raw sequencing data into clear, concise, and clinically relevant reports. Our platform automates the entire process, providing QC metrics, detailed variant information, and annotation from leading databases, empowering you to make informed decisions quickly and confidently.
Download ReportReady to Revolutionize Your Clinical Research?
Discover how GeneAssure Clinical can accelerate your variant discovery and reporting. Get in touch for a personalized demo and see the future of genomics, today.