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REPLI-g Single Cell RNA Library Kit
For RNA library construction from single cells for Illumina sequencing applications
    • Unbiased, PCR-free single cell library construction
    • Comprehensive and accurate transcriptome profiling of single cells
    • Fast time-to-result through a streamlined protocol
    • Minimal bias and sensitive detection of low-abundance transcripts
    • High-quality libraries, ready for use on any Illumina NGS platform
REPLI-g Single Cell Kit
For highly uniform whole genome amplification (WGA) from single cells or limited sample ...
    • WGA from single cell material with complete genome coverage
    • Unbiased amplification of genomic loci due to MDA technology
    • Optimized for use with new technologies, including NGS
    • Consistent yields of up to 40 µg (average product length >10 kb)
    • Novel tool for cancer research, stem cell research, or metagenomics
REPLI-g FFPE Kit
For direct whole genome amplification of DNA from formalin-fixed, paraffin-embedded ...
    • Whole genome amplification directly from paraffin sections
    • Whole genome amplification of purified DNA from FFPE tissue
    • Scalable and standardized DNA yields: up to 40 µg per tissue section
    • Fast and easy protocol for rapid results
GeneRead qPCR SYBR® Green Mastermix
For use with the GeneRead Library Quant System
    • Specific products with minimal primer–dimers
    • Instrument-specific all-in-one mixes
    • Available with ROX or fluorescein
Generation DNA Purif. Solution

For use with Generation Capture Kits in genomic DNA purification

    • Fast and easy protocol
    • Well-suited for standard PCR screening applications
    • Purified DNA is ready to use in standard PCR
GeneRead DNAseq Library Quant Array
For qPCR-enabled quantification of NGS libraries before sequencing
    • Predispensed sequentially diluted DNA standard; no manual titration
    • Quality score enables removal of low-quality libraries before sequencing
    • Data analysis Excel sheet automatically calculates library concentration
    • Simple protocol, high sensitivity, and wide dynamic range
    • Compatible with all major NGS platforms and qPCR instruments
GeneRead DNAseq Panel PCR Kit V2
For targeted enrichment prior to NGS using GeneRead DNAseq Panels V2
    • High degree of specificity and uniformity
    • Optimized for use with GeneRead DNAseq Panels V2
GeneRead DNA FFPE Kit
For efficient recovery of high-quality genomic DNA (gDNA) from formalin-fixed paraffin ...
    • Efficient recovery of gDNA from FFPE samples due to optimized lysis
    • Enzymatic removal of cytosine deamination artifacts
    • Minimized risk of false SNP calls
    • Outstanding results in DNA sequencing applications
    • Automation on the QIAcube 
QIAseq and GeneRead Library Prep Kits
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead Size Selection Kit
For quick and reliable removal of DNA fragments <150 bp for library ...
    • Precise size selection of DNA fragments
    • Fast procedure, based on QIAGEN’s proven silica-column technology
    • An easy-to-follow protocol, automatable on the QIAcube
GeneRead DNAseq Targeted Panels V2
For targeted enrichment of biologically and clinically relevant panels using any of 15 ...
    • Outstanding sequencing performance
    • As little as 10 ng DNA needed
    • Compatible with many samples types including FFPE samples
    • Can be used on any sequencing platform
    • Clinically and biologically focused content
GeneRead DNAseq Custom Panel V2
For targeted enrichment of a customized set of genes or genomic regions specific for your ...
    • Outstanding sequencing performance
    • As little as 10 ng DNA needed
    • Compatible with many samples types, including FFPE samples
    • Can be used on any sequencing platform
    • Customizable for any region in the genome
GeneRead DNA Library Q Kit
Automated and streamlined to save time
    • Affordable automation reducing hands-on time by up to 75%
    • Minimal input material of only 4ng needed
    • Experimentally verified with the entire Sample-to-Insight GeneReader NGS workflow
    • Can be paired with the QIAxcel for size-determination to further reduce hand-on time
GeneRead QIAact Actionable Insights Tumor Panel
For actionable tumor insights from FFPE and liquid biopsy samples
    • Designed to enrich for the genes and variants most relevant to your research
    • Proven performance with the GeneReader NGS System
    • Verified for use with DNA from FFPE samples and liquid biopsy samples
    • The first panel to be integrated as part of a complete end-to-end NGS workflow
GeneRead Clonal Amp Q Kit
For clonal amplification of DNA libraries for next-generation sequencing (NGS) ...
    • Generation of sequencing-ready amplified libraries
    • Multiplex clonal amplification: each library pool can include up to 12 uniquely bar coded DNA library samples
    • Automated on the GeneRead QIAcube
    • Proven performance with the GeneReader NGS System
GeneRead Sequencing Q Kits
For preparation of DNA sequencing for next-generation sequencing (NGS) ...
    • For high quality sequencing performance
    • Available in kits for multiple flow cell runs
    • Color-coded kit components for easy set-up
    • Proven performance with the GeneReader NGS System
GeneRead QIAcube
For automating and streamlining library template preparation 
    • Significant reduction of hands-on time and increased reproducibility
    • Scalable preparation of between 1 and 4 library sequencing template pools in parallel
    • Intuitive touchscreen guiding you through set-up
    • Built on the success of the QIAcube platform
    • Proven performance with the GeneReader NGS System
GeneRead DNAseq Mix-n-Match Panels V2
For targeted enrichment of a customizable gene panel using any of 570 laboratory-verified ...
    • Outstanding sequencing performance
    • As little as 40 ng DNA needed
    • Compatible with many samples types including FFPE samples
    • Can be used on any sequencing platform
    • Customizable using any of 570 pre-verified gene primer sets

GeneRead Link Software
For automated data transfer between the GeneReader NGS System and LIMS
    • Automated transfer of data from LIMS to the GeneReader NGS System and of results back to LIMS
    • Reduced time and effort for checking results
    • Traceability of all sample-related data
    • Proven performance with the GeneReader NGS System
GeneRead Library Quant System
For qPCR-enabled quantification of NGS libraries
    • Ready-to-use, predispensed, sequentially diluted DNA standard (array format)
    • Automatic calculation of library concentration
    • Simple protocol, high sensitivity, and wide dynamic range
    • Compatibility with Illumina and Ion Torrent/Proton NGS platforms
    • Compatibility with most qPCR instruments
GeneRead DNA I Amp Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead DNA QuantiMIZE Kits
For quantification and qualification of amplifiable DNA prior to NGS
    • Provides 2 qPCR assays dispensed onto arrays or in individual tubes
    • Quantifies and qualifies DNA that is amplifiable by PCR
    • Guides optimization of targeted enrichment conditions
    • Requires no serial dilutions
GeneRead DNA L Amp Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead DNA Library l Core Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead DNA L Core Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead QIAact Lung DNA Panel
For lung cancer insights from FFPE and liquid biopsy samples
    • All mutation types: SNVs, InDels and CNVs and fusions*
    • Higher sensitivity and more uniform coverage with the unique UMI technology
    • For use with FFPE and Liquid Biopsy samples
    • DNA cleanup steps fully automatable on the QIAcube instrument
    • Integrated as part of a complete sample-to-insight NGS workflow including full bioinformatics analysis and interpretation
QIAsymphony SP for FFPE sample preparation
For automated, high throughput DNA prep from FFPE tissue samples
    • Rapid purification of high-quality, ready-to-use DNA for use in research applications
    • Enzymatic removal of cytosine deamination artifacts for FFPE samples
    • Automation on the QIAsymphony Sample Preparation
    • Outstanding results in DNA sequencing applications
GeneRead QIAact BRCA 1/2 Panel
For breast and ovarian cancer insights from FFPE samples on the GeneReader NGS ...
    • Full coverage: all coding regions of BRCA 1 and 2 + 20 bp flanking intronic regions
    • All mutations: germline or somatic, mutations or deletions
    • Proven performance with automation on the GeneReader NGS System
    • Integrated as part of a complete Sample to Insight workflow including bioinformatics analysis and interpretation
QIAcube

For fully automated sample prep using QIAGEN spin-column kits

    • Automation of trusted QIAGEN spin-column kits
    • Elimination of manual processing steps
    • Purification of DNA, RNA, or proteins
    • More free time with affordable automated processing
    • Standardized results and increased productivity
QIAamp Circulating Nucleic Acid Kit

For isolation of free-circulating DNA and RNA from human plasma or serum

    • Concentration of nucleic acids, with high input and low elution volumes
    • Efficient recovery of fragmented DNA and RNA
    • No organic extraction or ethanol precipitation
    • Removal of contaminants and inhibitors
QIAamp DNA Microbiome Kit
For isolation of bacterial microbiome DNA from mixed samples
    • Isolation of bacterial DNA from swabs and body fluids
    • Effective depletion of host DNA
    • Optimized mechanical and chemical cell lysis
    • Ultra-clean columns to minimize contamination risk

     

QIAxpert System
For accelerated DNA, RNA, and protein quantification and quality control
    • Quantify nucleic acids from up to 16 samples in less than 2 minutes
    • Discriminate between molecules of interest using unique spectral protocols
    • Determine specific amounts of DNA, RNA, and other contaminating fractions
    • Rapidly perform analyses via the intuitive, full-color integrated touchscreen
    • Generate comprehensive reports to view on any computer or smart device
QIAGEN Clinical Insight (QCI) Analyze
The bioinformatic complement to the GeneReader NGS System
    • Optimized easy-to-use, pre-designed secondary data analysis pipelines
    • Role-based permissions for running, editing, reporting and customizing workflows
    • Fast and reliable globally-recognized algorithms
    • Unique user capability to filter, confirm or reject variants within the review process
    • Concise transparent reporting
GeneReader Platform
For next-generation sequencing applications 
    • The world’s first truly complete NGS workflow: Rely on one partner to provide a seamlessly integrated workflow offering ease of use and efficiency from Sample to Insight.
    • Actionable insights: Create relevant reports using QIAGEN’s proven gene panels and bioinformatics.
    • Flexibility to fit your needs: Scalable batch sizes and continuous loading of multiple flow cells enable you to adapt and scale the GeneReader NGS System to match your needs and grow.
    • Guaranteed results with predictable costs: Innovative commercial models such as price-per-insight options offer better cost management and low initial investment hurdles.
    • Proven expertise and service for our customers: Our teams at QIAGEN are ready to support you in efficiently implementing, validating and operating GeneReader in your lab.
QIAGEN Clinical Insight (QCI) Interpret
For NGS data interpretation and reporting
    • Transparent, evidence-based variant classification
    • Focused on actionable content from drug-labels and clinical trials to accelerate clinical research insights
    • Accesses manually curated clinical case counts and biological studies
    • Outputs clear, concise, referenced reports
    • Option to build your own private, experience-based database to increase speed and accuracy of subsequent interpretations
QIAseq Targeted DNA Custom Panels

Digital DNA sequencing to confidently detect low-frequency variants

    • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
    • Complete Sample to Insight solution streamlines the workflow
    • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
    • Minimal DNA input to preserve precious samples
    • Optimized buffers and conditions to achieve high coverage of GC-rich regions
    • Build and receive within two weeks a panel for your unique content
QIAseq Index Kits

For indexing samples enriched with either QIAseq Targeted DNA Panels or QIAseq Targeted ...

      • Sample indexes to index up to 384 samples for Illumina sequencers or 96 samples for Ion Torrent sequencers
      • Enough of each index for four samples
      • Modular indexing structure for Illumina
      • Tube format for flexibility and array format for convenience and high-throughput
    QIAseq Targeted DNA Panels

    Digital DNA sequencing to confidently detect low-frequency variants

      • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
      • Complete Sample to Insight solution streamlines the workflow
      • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
      • Minimal DNA input to preserve precious samples
      • Optimized buffers and conditions to achieve high coverage of GC-rich regions
    QIAseq DNA QuantiMIZE Kits
    For quantification and qualification of amplifiable DNA prior to NGS
      • Provides 2 qPCR assays dispensed onto arrays or in individual tubes
      • Quantifies and qualifies DNA that is amplifiable by PCR
      • Guides optimization of targeted enrichment conditions
      • Requires no serial dilutions
    QIAseq Library Quant System
    For qPCR-enabled quantification of NGS libraries
      • Ready-to-use, predispensed, sequentially diluted DNA standard (array format)
      • Automatic calculation of library concentration
      • Simple protocol, high sensitivity, and wide dynamic range
      • Compatibility with Illumina and Ion Torrent/Proton NGS platforms
      • Compatibility with most qPCR instruments
    QIAseq cfDNA All-in-One Kits
    For conversion of cfDNA from plasma to NGS library for any liquid biopsy samples
      • Optimal conversion of cfDNA at every step from plasma to NGS library through highly efficient ligation chemistry 
      • Go directly from eluant to library prep without quantification using a protocol supporting the widest range of cfDNA input (1–100ng)  
      • Generate PCR-free libraries from 10 ng of cfDNA
      • Minimize PCR bias by the use of high-fidelity amplification reagents
      • Reduce cross-contamination risk with pre-dispensed plate-based adapters for up to 96 samples/NGS run
    QIAseq FX DNA Library Kit

    High-quality whole genome libraries – no shearing required!

      • DNA fragmentation to NGS-ready libraries – all in a single kit
      • Streamlined 2.5-hour workflow for easy automation
      • High library complexity and even coverage maximizes interpretable data
      • Flexible DNA inputs of 1 ng –1 µg 
      • Customizable fragment and batch sizes match any whole genome or hybrid capture workflow
    QIAseq FX Single Cell DNA Library Kit

    Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity

      • Whole genome libraries from single cells in under 4 hours
      • Maximize genome coverage, don’t miss important features
      • Best-in-class sequence fidelity reduces false-positives
      • Delivers PCR-free NGS libraries and amplified gDNA for followup testing
      • Analyze sequence and copy-number variations anywhere in the genome


    QIAseq Ultralow Input Library Kit
    For preparation of DNA libraries for next-generation sequencing (NGS) applications that ...
      • Ultra-efficient chemistries maximize performance of sub-nanogram samples
      • Flexible protocol provides a comprehensive solution for 10 pg−100 ng DNA input
      • Automation-friendly, dual-barcoded adapter plate included in 96-reaction kit 
      • Compatible with a wide range of sample types, including cfDNA, FFPE, ancient DNA and ChIP-seq

    QIAseq FX Single Cell RNA Library Kit

    Single cell RNA-seq libraries that provide a deeper view of the transcriptome

      • Higher diversity libraries detect more transcripts, including mRNA and lncRNA
      • PCR-free protocol reduces bias and provides great reproducibility
      • Sequencing ready libraries from isolated single cells in just 5.5 hours



    QIAsymphony RGQ

    Integrated automated sample preparation and assay setup, with manual transfer to the ...

      • Unprecedented flexibility
      • Workflow optimization and utility
      • Maximized ease of use and convenience
      • Regulated assays and laboratory-developed tests
      • Designed for largest range of applications
    QIAseq Targeted RNA Virtual Panels

    Digital RNAseq for gene expression profiling

      • Add up to 25 genes to a catalog panel 
      • Use only 25 ng of total RNA for each panel
      • Go from sample to sequence-ready library in 1 day
      • Molecular barcodes ensure accurate expression profiling
    QIAseq Targeted RNA Custom Panels

    For digital RNA-seq for gene expression profiling

      • Use up to 1000 mRNAs or lncRNAs per panel
      • Start with 25 ng of total RNA for each panel
      • Molecular barcodes ensure accurate expression profiling
      • Go from sample to sequence-ready library in 1 day
    QIAseq Targeted RNA Extended Panels

    Digital RNAseq for gene expression profiling

      • Add up to 25 genes to a catalog panel 
      • Use only 25 ng of total RNA for each panel
      • Go from sample to sequence-ready library in 1 day
      • Molecular barcodes ensure accurate expression profiling
    QIAseq Targeted RNAscan Panels
    Applying digital RNA sequencing to scan for known and novel fusion genes
      • Accurate quantification of a large number of fusion genes
      • Identify new fusion gene partners, no prior knowledge of breakpoint needed
      • Works with low-quality RNA, including RNA from FFPE and liquid biopsy
      • Requires low RNA input, as low as 15 ng of un-enriched RNA
      • Automation-friendly


    QIAseq Targeted RNA Panels
    Digital RNAseq for gene expression profiling
      • Molecular barcodes remove PCR and library construction bias
      • Start with only 25 ng of total RNA
      • Simple 1 day library construction workflow
      • Use with any illumina or Thermo-Fisher NGS instrument
    QIAseq Targeted RNA Indexes

    For indexing samples for targeted RNA sequencing and primers necessary for sequencing RNA ...

        • Sample indexes to index up to 96 samples for Illumina and Ion Torrent sequencers
        • Enough of each index for four samples
        • Tube format for flexibility and array format for convenience and high-throughput
      QIAseq 1-Step Amplicon DNA Library Kit
      For fast and efficient preparation of DNA libraries for use in NGS applications
        • Fast, one-tube procedure that allows up to 50% time savings
        • High yields from minimal amounts of starting material
        • Unbiased amplification with an optional, high-fidelity amplification step
        • Multiplexing, high-throughput capability
      QIAseq Targeted DNA Extended Panels

      Digital DNA sequencing to confidently detect low-frequency variants

        • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
        • Complete Sample to Insight solution streamlines the workflow
        • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
        • Minimal DNA input to preserve precious samples
        • Optimized buffers and conditions to achieve high coverage of GC-rich regions
        • Add up to 100 primers to extend the content of a cataloged panel
      QIAscout
      For accessible, affordable and efficient isolation and recovery of single cells
        • Works in conjunction with most inverted microscopes
        • Ideal for a variety of eukaryotic cells
        • Cell viability and purity maintained after isolation
        • Isolated cells suitable for use in various single-cell workflows
      QIAseq Targeted DNA Booster Panels

      Digital DNA sequencing to confidently detect low-frequency variants

        • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
        • Complete Sample to Insight solution streamlines the workflow
        • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
        • Minimal DNA input to preserve precious samples
        • Optimized buffers and conditions to achieve high coverage of GC-rich regions
        • Boost the performance of some primers or extend the content of a custom panel
      QIAseq Targeted RNAscan Custom Panel
      Applying digital RNA sequencing to scan for known and novel fusion genes
        • Accurate quantification of a large number of fusion genes
        • Identify new fusion gene partners, no prior knowledge of breakpoint needed
        • Works with low-quality RNA, including RNA from FFPE and liquid biopsy
        • Requires low RNA input, as low as 15 ng of un-enriched RNA
        • Build and receive within two weeks a panel for your unique content
      QIAseq miRNA Library Kit

      Gel-free miRNA Sample to Insight solution for differential expression analysis and novel ...

        • Gel-free miRNA sequencing library prep from as little as 1 ng of total RNA
        • Elimination of adapter dimers and unwanted RNA species resulting in the highest fidelity and most efficient data
        • Bead based method to remove adapter dimers and unwanted RNA species
        • Integrated Unique Molecular Indices (UMIs) enable quantification of individual miRNA molecules
        • Primary read mapping and differential expression analysis via the GeneGlobe Data Analysis Center