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.More about user-friendliness and scalability
CLC Genomics Server and Biomedical Genomics Server give you full control over your data processing — for any volume of data — and let you keep your data on premises, 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.Read more about Biomedical Genomics Workbench
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.Read more about scalable whole genome analysis
At the core of our High Volume Sequencing Solutions are both CLC Genomics Server and Biomedical Genomics Server, which are designed to meet project requirements now and into 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.Focus on what matters
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
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.
© QIAGEN 2019. All rights reserved - Trademarks & Disclaimers