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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
MagAttract HMW DNA Kit
For isolation of high-molecular-weight genomic DNA
    • Reproducible isolation of high-molecular-weight DNA
    • High yields and purity from a range of sample materials
    • Fast and convenient protocols
    • Complete removal of inhibitors
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
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 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 
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 Pure mRNA Kit
For highly selective and efficient purification of mRNA for NGS applications
    • Efficient removal of almost all rRNAs (significantly >99%)
    • No bias from unintended removal of poly A+ mRNAs
    • As little as 100 ng – 5 μg total RNA required
    • Maximal convenience, minimal hands-on time
    • Automation on the QIAcube
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 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 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 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 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 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 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 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
GeneRead QIAact Lung DNA Panel
For lung cancer insights from FFPE and liquid biopsy samples
    • All mutation types: SNVs, InDels and CNVs and fusions*
    • Developed in collaboration with world top lung cancer experts
    • Higher sensitivity and more uniform coverage with the unique UMI technology
    • For use with FFPE and Liquid Biopsy samples
    • 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
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
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
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

     

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
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
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.
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 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



    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

    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
    QIAsymphony SP/AS instruments
    For fully integrated automation of complete workflows, from sample preparation to assay ...
      • Innovative, easy-to-use modular system with built-in touchscreen.
      • Purification of DNA and RNA from a wide range of samples
      • Automatic transfer of eluates to the QIAsymphony AS for assay setup
      • Continuous sample loading, with bar code reading for sample tracking
      • Import of sample lists and export of sample sheets
    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 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 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 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 Library Kit
      For fast and efficient preparation of DNA libraries for use in NGS applications
        • One-tube, benchtop library prep from PCR products in just 30 minutes
        • Maximal convenience with automatable, 1-reaction, room-temperature setup
        • High-quality, artifact-free libraries, ready for use on any Illumina NGS platform
        • Compatible with any gene panel or PCR product, only needs 1 ng input DNA
        • Single-use adapter plates minimize risk of contamination or handling errors
      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
      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
      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 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
      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
      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