Accuracy, scalability,
and performance

Our High Volume Sequencing Solutions not only provide accuracy, but are also scalable to the most extreme throughputs of whole human genome data, and their robustness ensures that they can easily handle future development. Our solutions keep costs per sample low without compromising quality, and are among the most accurate in both variant calling and interpretation. They are developed under the ISO 9001 Quality Management System and are audited and approved with excellence by a third party.



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 and Biomedical Genomics Server offer central storage, data management, and seamless, efficient data sharing and collaboration capabilities. Using CLC Genomics Workbench and/or Biomedical 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.




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