CLC Genomics Workbench
A comprehensive and user-friendly analysis package for analyzing, comparing, and visualizing next generation sequencing data.
Analyze, compare and visualize NGS data
Dominating the high-throughput sequencing data
We have overcome the challenge to analyze high-throughput sequencing data faster than it is produced by implementing a SIMD-accelerated assembly algorithm in our next generation sequencing solution, CLC Genomics Workbench – a cross-platform desktop application with a graphical user-interface.
CLC Genomics Workbench, for analyzing and visualizing next generation sequencing data, incorporates cutting-edge technology and algorithms, while also supporting and integrating with the rest of your typical NGS workflow.
CLC Genomics Workbench is available for Windows, Mac OS X, and Linux platforms. It includes a number of features within the fields of genomics, transcriptomics and epigenomics, and additionally it includes all the tools of CLC Main Workbench.
We support all the major next generation sequencing platforms, such as SOLiD, Ion Torrent, Complete Genomics, 454, Illumina Genome Analyzer and of course also Sanger, and we are working closely together with all the instrument vendors to ensure full integration in the ongoing development.
CLC Genomics Workbench supports read mapping as well as de novo assembly of hybrid data.
View the list of the latest improvements of CLC Genomics WorkbenchDownload CLC Genomics Workbench product sheet Request a quote
Benchmarks on human data sets
Runtime measurements for 1.34 billion paired-end Illumina reads. Our read mapper completes within nearly 17 hours which is approximately a 10-fold acceleration compared to our previous mapper.
Runtime measurements for 2.8 million 454-Titanium reads mapping in 13 minutes.
Benchmarking hardware: Benchmarks have been executed on a dedicated CLC Genomics MachineDownload our white paper on read mapping
CLC Genomics Workbench incorporates cutting-edge technology and algorithms, while also supporting and integrating with the rest of your typical NGS workflow. CLC Genomics Workbench supports key next generation sequencing features within genomics, transcriptomics and epigenomics, and additionally it includes all the tools of CLC Main Workbench.
Read more detailed information on
- Read mapping
- De novo assembly
- Variant Detection
- Trio Analysis
- and many more features
Read more details on the specific features on our ‘Features’ page
You can also see a list of all features of CLC Genomics Workbench