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Full control of high-volume sequencing data

The falling cost of sequencing is changing science and healthcare. Sequencing is driving the creation of technologies that quickly generate, manage and extrapolate massive volumes of data. For population-scale studies and clinical usage models, cost-effective bioinformatics solutions are imperative.



Secure and high performance computing

CLC Genomics Server gives you full control over your data processing — for any volume of data — and lets you keep your data on-premise, under your security policy. In addition to data security, these solutions also provide budget security, with lower cost of ownership per sample.

Our proven High Volume Sequencing Solutions allow you to work with our user-friendly desktop software as your interface, negating the need for complexity while leveraging high-performance cluster infrastructures.


Expandable and customizable solutions

At the core of our High Volume Sequencing Solutions is CLC Genomics Server, which is designed to meet project requirements now and in the future. The system’s open design easily integrates with current and future IT infrastructures, such as scheduling systems, user directories and other third party software — whether commercial or open-source. Our mature APIs and SDK allow plugins to extend the solution.

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There is no doubt that data analysis is still the major bottleneck in NGS workflow. We now can keep the primary data analysis and evaluate the data reliability and fidelity in-house without outsourcing services.

Ching-Chun Lin – Research Manager, Academia Sinica


Seamless data-centric collaboration

As a central part of our High Volume Sequencing Solution, CLC Genomics Server offers central storage, data management, and seamless, efficient data sharing and collaboration capabilities. Using CLC Genomics Workbench as the front-end enables user authentication, support for user/group directories and a mature access privilege system that secures data permissions for each end user. Our solutions also integrate with existing user directories, such as Microsoft Active Directory and various other LDAP implementations. Our ability to expand these servers with your own scripts, command-line tools, plugins and well-designed graphical interfaces, removes a bottleneck that exists between the bioinformatics core and the scientific users.