ProductFinder helps you to find the best QIAGEN product for your application. Make your selections and you will find the most suitable products.

10 results found with selected category.

Biomedical Genomics Workbench

For analyzing, comparing and visualizing human hereditary and cancer NGS data for ...

    • Quickly analyze complex data
    • High accuracy for low-frequency variant detection
    • Modify or personalize analysis workflows
    • Conveniently filter and visualize data
    • Compare results with relevant databases

The gold standard resource for comprehensive data on published human inherited disease ...

    • 170,000+ mutation reports including specifics on genome coordinates, sequence details, and links to the source reference as well as public resources like dbSNP and OMIM
    • 6,800+ summary reports listing all known inherited disease mutations for a given gene characterized by six different pathogenic variant classes
    • Advanced search functionality, including the ability to find mutations based on the type of nucleotide or amino acid change, or their location in a specific motif, splice site, or regulatory region


Workbench Modules
For enhancing functionalities of CLC Genomics Workbench, Biomedical Genomics Workbench, ...
    • The modules have an intuitive and user-friendly interface
    • They incorporate cutting-edge technology and algorithms
CLC Main Workbench
For advanced DNA, RNA, and protein analyses
    • A comprehensive workbench for advanced DNA, RNA, and protein analyses
    • An intuitive graphical user-interface
    • Support for efficient data sharing between colleagues and collaborators
    • Frequent updates with the latest scientific developments
CLC Assembly Cell
A high-performance computing solution for mapping reads to a reference and de novo ...
    • Read mapping of Illumina, Pacific Biosciences, Ion Torrent, SOLiD, and 454 sequencing data

    • De novo assembly of Illumina, Pacific Biosciences, Ion Torrent and 454 sequencing data

    • Support for both short read and long read assembly and mapping

For researching and cross-referencing syndrome information
    • Provides detailed information about key clinical attributes
    • Differential diagnoses can be made
    • Helps in the diagnosis of patient syndromes by providing imaging and genetics
Ingenuity Variant Analysis
For identifying disease-causing variants from human whole genome, exome and gene ...
    • Intuitive, user-friendly interface with no bioinformatics skills needed
    • Interactive filters narrow down the search for causal variants
    • Web-based application compliant with HIPAA and Safe Harbor standards
    • Sharing and publication tools for collaboration and manuscript preparation
Ingenuity Pathway Analysis (IPA)
For modeling, analyzing, and understanding complex 'omics data
    • Analysis of gene expression/miRNA/SNP microarray data
    • Deeper understanding of metabolomics, proteomics, and RNAseq data
    • Identification of upstream regulators
    • Insight into molecular and chemical interactions and cellular phenotypes
    • Discoveries about disease processes
CLC Genomics Workbench
For analyzing, comparing, and visualizing next-generation sequencing data
    • Cross-platform desktop application with an intuitive and user-friendly interface
    • Incorporates cutting-edge technology and algorithms
    • Includes numerous features in genomics, transcriptomics, and epigenomics
    • Supports all major next-generation sequencing platforms
GeneGlobe Data Analysis Center
For analyzing and interpreting real-time PCR or NGS data
    • Intuitive, user-friendly interface with no bioinformatics skills needed
    • Complimentary data analysis for all GeneGlobe assays and arrays
    • Get results in scatter plot, volcano plot, clustergram and heat map formats