NGS Data Analysis Platform
Professional laboratory testing and analysis services with state-of-the-art technology and expert scientific support.
Service Description
Gentaur provides NGS Bioinformatics Analysis Services to support research laboratories, sequencing facilities, and biotechnology companies in converting next-generation sequencing (NGS) data into reliable, interpretable results. This service eliminates the need for in-house bioinformatics infrastructure while ensuring secure, reproducible, and scalable analysis workflows.
Supported NGS Applications
The service supports a wide range of sequencing applications, including:
- RNA sequencing (RNA-seq).
- Whole-genome sequencing (WGS).
- Whole-exome sequencing (WES).
- Targeted DNA sequencing.
- Variant detection and annotation.
All workflows are built using validated and standardised pipelines, ensuring consistent results suitable for research reporting and downstream analysis.
Secure and Flexible Data Handling
Gentaur offers flexible data handling options adapted to institutional requirements. Analyses can be performed using secure cloud environments, including Bring Your Own Cloud (BYOC) configurations, allowing customers to maintain full control over data ownership, governance, and compliance.
This approach minimises data transfer risks while enabling efficient use of scalable computing resources.
End-to-End Scientific Support
Each project is accompanied by dedicated customer and scientific support, including:
- Pre-analysis consultation and workflow selection
- Assistance with data preparation and upload
- Technical support during analysis execution
- Guidance on result interpretation and reporting
This ensures that both bench scientists and bioinformatics teams receive practical, human support throughout the project lifecycle.
Reproducibility and Reliability
All analyses are performed using reproducible, version-controlled workflows, supporting consistent results across projects and long-term studies. This is particularly valuable for collaborative research, sequencing cores, and multi-year projects.
Who This Service Is For ?
This service is suitable for :
- Academic and clinical research laboratories
- Sequencing core facilities
- Biotech and pharmaceutical R&D teams
- CROs and assay developers
- Research groups working with large or complex NGS datasets