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Description
GenomiX is an end-to-end genomics analytics platform designed to unify NHS-grade clinical genomics, flexible bioinformatics research, and AI-powered insights. It addresses the biggest challenges in the field, from handling massive raw sequencing files to harmonizing data across fragmented systems like EHRs, LIMS, and CRO platforms. Its cloud-agnostic and container-native architecture allows deployment on AWS, Azure, or GCP while supporting orchestration via Kubernetes and workflow engines such as Nextflow, CWL, and Snakemake. The platform delivers real-time data ingestion, tiered storage with lifecycle automation, and advanced metadata harmonization for structured insights. Integrated visualization tools and machine learning models like CNNs, BERT, and DESeq2 provide deeper analytics and predictive power. GenomiX also enables reproducibility with Git versioning, CI/CD pipelines, and customizable tool integration. Security is core, offering role-based access, full audit trails, NHS interoperability via FHIR, and certifications aligned with GDPR and HIPAA. By combining scalability, compliance, and innovation, GenomiX accelerates clinical research, enhances collaboration, and drives progress in personalized medicine.
Description
Efficiently generating reports for NGS-based clinical tests necessitates a well-established and sophisticated platform that can automatically prioritize variants, interpret clinical data, and create comprehensive reports. Strand Omics serves as a rapid, HIPAA-compliant cloud platform that enhances our clinical diagnostics efforts, having been refined over four years through the analysis of more than 10,000 clinical reports and numerous peer-reviewed studies. This platform integrates advanced bioinformatics algorithms with curated databases, intuitive visualization tools, and robust reporting features. It is designed with specialized workflows tailored for both rare inherited conditions and somatic tumor profiling assays. Additionally, the system boasts a library of over 10,000 somatic variants that have been curated for their oncogenic potential, alongside 100 genes selected for their druggability across various cancer types, as well as 500 drugs that have been validated for efficacy against multiple cancers. Furthermore, its comprehensive approach ensures that healthcare professionals have access to critical data, ultimately facilitating informed decision-making in patient care.
API Access
Has API
API Access
Has API
Integrations
No details available.
Integrations
No details available.
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
VE3 Global
Founded
2025
Country
United Kingdom
Website
www.ve3.global/solutions/ve3-genomics-accelerator-solution/
Vendor Details
Company Name
Strand Life Sciences
Founded
2000
Country
India
Website
strandls.com/bioinformatics/
Product Features
Product Features
Scientific Data Management System (SDMS)
Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows