CLC Genomics Workbench 11

Featuring improved NGS read handling and read-through adapter trimming for error reduction

Explore release highlights

End-to-end NGS data analysis solution

CLC Genomics Workbench is a powerful solution developed by scientists for scientists to analyze and visualize next generation sequencing (NGS) data. Its cutting-edge technology incorporates unique features and algorithms that are widely used by scientific leaders in industry and academia to overcome bottleneck challenges associated with data analysis.

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Download and install CLC Genomics Workbench

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CLC Genomics Workbench is developed for Windows, Mac and Linux. Download now to start your data analysis. To get started follow the step by step instructions in the user-friendly manual or watch the tutorials in our resources guide.





Customized workflows to accelerate your data analysis

CLC Genomics Workbench is developed to support a wide range of NGS bioinformatics applications. Workflows can combine quality control steps, adapter trimming, read mapping, variant detection, and multiple filtering and annotation steps into a pipeline you can share with colleagues and execute with just one click.


From sample to insight with QIAGEN Bioinformatics

System requirements

The CLC Genomics Workbench system requirements are available on our general system requirements page and also in the user manual.

Latest improvements

We frequently release updates and improvements such as new functionalities, bug fixes or plugins. To get a complete overview, please read the latest improvements.

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