Rapidly identify the best biomarker and target candidates based on biological characteristics most relevant to your discovery study. Our powerful and high-quality tools are driven by over 20 million scientific findings and over 500,000 samples, to save you valuable time and resources while empowering your biomarker research by driving new discoveries.
Explore our NGS and ‘omics data analysis tools for:
• Ready-to-use and flexible workflows: Over a dozen pre-built workflows to accelerate analysis of your cancer and hereditary disease data. Build your own customized analysis workflows for a wide range of both DNA and RNA sequencing data
• Intuitive interface: Interactive visualization of your data linked to a best-in-class track viewer
• Visualize and share results with the built-in Genome Viewer
• Platform independent: Supports common sequencing platforms (Illumina, Ion Torrent, PacBio, Oxford Nanopore and GeneReader) and runs on most operating systems
• Enterprise ready: Support multiple users in an intuitive way, with high-throughput analysis and automation
User-friendly bioinformatics software solutions enable a comprehensive analysis of your NGS data. QIAGEN CLC Main Workbench offers core workflows such as DNA and gene expression, primer design, molecular cloning, phylogenetic analyses and data management. QIAGEN CLC Genomics Workbench provides advanced workflows for 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).
Uncover critical correlations among microbiota, metagenome and host. Easily understand complex metagenomic data through tools and streamlined analysis workflows for gene finding, annotation, taxonomic and functional microbiome analysis. Our solutions for microbial genomics include tools and workflows for a broad range of bioinformatics needs for microbiome analysis, isolate characterization, functional metagenomics, pathogenicity, strain typing and resistance identification.
Empower your biomedical analyses with prebuilt workflows for human, mouse and rat genomics, including support for QIAseq UMI-based NGS library preparation kits and panels. Content includes hereditary disease workflows, oncology somatic mutation detection workflows for cancer FFPE or liquid biopsy (single sample or matched tumor-normal) samples, sensitive detection of SNPs, MNVs, tandem repeats, structural variants, fusion genes and CNVs.
Grow and scale your NGS capabilities beyond the number of available desktops. Our enterprise NGS solution can be deployed on a local server that manages the submission of many jobs via its own queuing system or through submission of jobs to a third-party grid scheduler. QIAGEN CLC Genomics Cloud Engine makes bioinformatics analysis scalable and accessible to anyone involved in the analysis of NGS data. It lets you build your workflows locally in the QIAGEN CLC Genomics Workbench and then deploy them on Amazon Web Services (AWS) in minutes.
With over 30 plugins and modules, these feature-rich extensions are seamlessly integrated and provide advanced tools and workflows to meet your specific analysis needs. Some of the most popular plugins include:
Explore the full list of available plugins:
The command-line interface of QIAGEN CLC Assembly Cell offers key features to support your assembly projects. These include read mapping, de novo assembly, quality trimming and removal of duplicate reads, as well as further functionalities in scripts and other next-generation sequencing workflows. Run it on your desktop computer or on a large computer cluster. QIAGEN CLC Assembly Cell is accelerated through advanced algorithm implementations which make the software one of the fastest and most accurate packages for NGS data analysis on the market.
Request a consultation with one of our bioinformatics specialists to discuss your specific research requirements.
Insightful data analysis and interpretation to understand your experimental results within the context of biological systems
Identify and explore contextual data in seconds, featuring an extensive collection of highly curated ‘omics data
Expand your clinical interpretation with expert-curated software for variant classification of any assay, covering any indication, on your sequencing platform