Install CLC Genomics Workbench

About CLC Genomics Workbench

Access all the tools you need for data analysis with our comprehensive solution. Start shifting your focus from data to discovery and take advantage of NGS workflows, interpretation and visualization.

What's new in 26.0.2

QIAGEN CLC Genomics Workbench Improvements - A link to the Modify a Workflow tutorial, which steps through creation of a customized analysis pipeline by editing an existing workflow, has been added to the Workbench background canvas. - The minimum coverage of target region positions from QC for Targeted Sequencing reports can be selected for inclusion in reports generated by Create Sample Report and Combine Reports. - Detect Fusion Genes from DNA adds "Fusion pair" information for fusions reported when "Include all fusions in the track output" is checked but where there is no fusion crossing reads supporting the fusion. This addition provides better support for downstream filtering. - Iterate workflow elements can now be connected downstream of Differential Expression for RNA-Seq, enabling downstream filtering when multiple statistical comparisons are produced. - Using left or right arrow navigation buttons in a variant track jumps the focus to the next visible variant. Previously, focus was moved to the next variant, even if it was hidden due to view settings in the Side Panel. - Exporting PDFs of reports that contain plots with many points is faster than previously. - Various minor improvements Bug fixes - Fixed an issue where Detect and Refine Fusion Genes sometimes output fusions with duplicated "Fusion pair" values when "Include all fusions in the WT track output" was checked. This could cause VCF export to fail and filtering tools to keep or remove too many fusions. See the public notification about this issue. - Fixed an issue in Create Sequence Constructs where, whe...

Version history