Genomics Research Infrastructure
While we are gearing up to become a fully open-access service platform, you can already register your interest now to receive status updates including when we are ready to open our services.
GRI is funded by Novo Nordisk Foundation grant NNF25SA0112666.
As soon as the Genomics Research Infrastructure opens to all, we will provide a comprehensive set of service from sample to data:
Diverse Functional Genomics Applications
GRI supports a diverse set of genomics applications and sample types, providing flexibility across research areas and project scales. In close dialogue with researchers GRI support is tailored to different phases of a project, including standard and non-standard library preparations, custom sequencing requirements, and innovative experimental approaches.
Training and User Support
We offer hands-on training and guidance, enabling new and experienced users to confidently plan and carry out functional genomics projects.
Efficient Turnaround
Our workflows are designed to ensure timely delivery, with typical turnaround times of approximately one week from receipt of sequencing-ready libraries to data delivery.
Established Technology Platform
Our infrastructure is based on a set of top-notch, robust and versatile technologies, including:
- Illumina NextSeq2000 (3 instruments)
- Agilent TapeStation 4200
- 10x Genomics Chromium X
This setup guarantees both flexibility and reliability of operations, with parallel sequencing capacity supporting consistent turnaround times and minimizing the risk of delays in case of instrument downtime.
Standardized Data Analysis
Data processing is based on widely adopted, community-developed pipelines, ensuring reproducible results.
Ready-to-Use Computing Environment
A dedicated high-performance computing (HPC) environment is available for further analysis of data generated at GRI, enabling efficient and scalable data processing.