QIAGEN CLC Genomics Workbench
QIAGEN CLC Genomics Workbench is a graphical user interface (GUI) based bioinformatics software. It houses tools for molecular biology and next generation sequencing (NGS) analysis.
CLC genomics workbench functionality includes: Analysis of your NGS data, including de novo assembly of whole genomes and transcriptomes, resequencing analysis (WGS, WES and targeted panel support), variant calling, RNA-seq, ChIP-seq and DNA methylation (bisulfite sequencing analysis), and access to plug-ins.
Premium Modules
NCI licenses do not include access to premium modules such as the Microbial Genomics Module and the Single Cell Analysis Module. If you are interested in these modules, please contact us at ncibtep@nih.gov.
Why QIAGEN CLC Genomics Workbench?
CLC is a single toolkit for all NGS analysis applications. Some key features are integrated analytics, ready-to-use workflows, custom workflow capability, and accurate performance. CLC is wizard driven to assist beginners through advanced users.
--- Event Contributor, Kristina Pinardo (Customer Solutions Manager, QIAGEN)
Access CLC Genomics Workbench
License type: NCI wide
You must submit a request through service.cancer.gov to obtain access to CLC Genomics Workbench. This software requires access to a floating license server (three simultaneous users), and so care should be taken to return the license when the software is not actively being used (i.e. close the application). Working with CLC Genomics Workbench requires login to the NIH network or VPN connection if remote.
NIH Library Access
There is a single static license available for use at the NIH library (in person) if you are not within NCI. See here for more information.
Event Slides and Other Resources
Additional Information
Check out additional information on QIAGEN CLC Genomics Workbench, including useful links, in the BTEP Resource pages.
For technical support questions, feel free to contact the Qiagen technical support team directly.