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QIAGEN CLC Genomics Workbench: NGS data analysis for any species, any platform, any workflow

QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. Cutting-edge technology and unique features and algorithms widely used by scientific leaders in industry and academia make it easy to overcome challenges associated with data analysis.

Scale your research using QIAGEN CLC Genomics Workbench 21

Now featuring sanger sequencing workflows, performance boost, long read RNA-sequencing analysis, haplotype caller* and HID panel support*.

Read about the latest improvements.

Need a full set of features, including microbial and metagenomics, single cell analysis or processing of small genomes? Discover our full-featured solution, QIAGEN CLC Genomics Workbench Premium.

 

Complete toolkit for genomics, transcriptomics, epigenomics, and metagenomics in one program

Comprehensive NGS data analysis

User-friendly bioinformatics software solutions allow for comprehensive 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).

Analyze your RNA-seq and small RNA (miRNA, lncRNA) data with easy-to-use transcriptomics workflows for differential expression analysis at gene and transcript levels.

Supported NGS platforms include Illumina, IonTorrent, Oxford Nanopore and PacBio.  

Biomedical genomics analysis

Biomedical genomics analysis and panel data analysis functionality is delivered through the QIAGEN CLC Genomics Workbench and the free plugin, Biomedical Genomics Analysis. This plugin provides tools and workflows for NGS panel data analysis, including WES, WGS, RNA-seq and QIAseq SARS-CoV-2 panel analysis workflows. 

Ready-to-use workflows

Biomedical workflows with complete reference sets for human, mouse and rat genomics include hereditary disease workflows (trio analysis, family-of-four) and oncology somatic mutation detection workflows, and can be used on FFPE or liquid biopsy samples (single sample or tumor-normal matched samples). These workflows enable sensitive detection of SNPs, MNVs, InDels, tandem repeats, structural variants, fusion genes, CNVs and loss of heterozygosity (LoH). Annotation with conservation scores and filtering steps on dbSNP and ClinVar are included.

Extend the toolbox with plugins

Multiple plugins are available for the QIAGEN CLC Genomics Workbench, tailored to specific applications such as multiple sequence alignment, whole genome alignment, transcript discovery, biomedical genomics analysis, long read analysis and haplotype calling*. These feature-rich extensions are seamlessly integrated into the QIAGEN CLC Genomics Workbench, and provide advanced tools and workflows to meet your specific needs for analysis.

Uncover the signals that lead to breakthrough discoveries in your biomedical research

Support for the analysis of NGS data from human and mouse PCR-based GeneRead panels or Unique Molecular Index (UMI)-based miRNA, RNA, DNA and methylation QIAseq panels is also provided by the Biomedical Genomics Analysis plugin. The tools and workflows work as well with third-party vendor NGS panels (PCR, UMI or hybrid capture target enrichment panels such as Illumina TSO500, Ion Torrent, ArcherDx, Agilent, NimbleGen or Twist panels). Read our Case Study: Qiaseq Myeloid Neoplasm Panel

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Don’t take our word for it: Hear what our customers have to say

QIAGEN CLC Genomics Workbench has contributed to tens of thousands scientific articles, and is by far one of the most highly-cited scientific software for molecular biologists and biomedical professionals.

Enhancing your productivity is our business.

QIAGEN CLC Genomics Workbench allows scaling to any size. Enterprise solutions permit entire institutions to make use of the same software.

Customized workflows to accelerate your data analysis

QIAGEN 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.

New workflow elements together with enhanced metadata capabilities allow within-workflow batching, useful for e.g., iterating the quantification of many RNA-seq samples followed by statistical comparison of groups.

From sample to insight with QIAGEN Digital Insights

From QIAGEN CLC Genomics Workbench you have easy access to pre-formatted reference data sets for many species. You can also submit results to other solutions in the QIAGEN Digital Insights portfolio, such as Ingenuity Pathway Analysis (IPA), QIAGEN Clinical Insights Interpret (QCI) and QIAGEN Clinical Insights Interpret Translational (QCI-IT).

 

Explore QIAGEN IPA   Explore QCI  Explore QCI Interpret Translational  

 

System requirements

The QIAGEN 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.

Download and install QIAGEN CLC Genomics Workbench

Enjoy a FREE full-feature trial for 14 days

QIAGEN 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.

*Exected release date for haplotype caller and HID panel support: February 15, 2021