Next-Generation Sequencing

Accelerate your NGS performance through Sample to Insight solutions

High-throughput next-generation sequencing (NGS) technologies continue to provide a wealth of sequence information, resulting in significant advances and new discoveries in a wide range of research areas. To enhance your specific NGS-based research and help you achieve your goals, we provide dedicated NGS target enrichment, library preparation and single cell solutions that eliminate bias and deliver uniform coverage. Our streamlined protocols are easy to use and automate seamlessly integrating workflows to use the full power of next-generation sequencing. Together we are making improvements in life possible.

Browse Next-Generation Sequencing

GeneRead QIAact AIT DNA UMI Panel
GeneRead QIAact AIT DNA UMI Panel
For even more actionable solid tumor insights from FFPE samples
QIAseq FX DNA Library Kit
QIAseq FX DNA Library Kit
All-enzymatic whole genome and hybrid capture library preparation for Illumina instruments with minimal bias
QIAseq Multimodal Custom Panels
QIAseq Multimodal Custom Panels
A single day sample to sequencing workflow for simultaneous enrichment and profiling of DNA variants, RNA fusions and gene expression levels from one sample input, as low as 10 ng
QIAxcel DNA Kits
QIAxcel DNA Kits
For automated analysis of DNA fragments using QIAxcel instruments
QIAseq Stranded RNA Library Kits
QIAseq Stranded RNA Library Kits
For preparation of stranded whole transcriptome RNA-seq libraries for NGS applications on Illumina instruments, including optional purification of poly A+ RNA from total RNA
QIAGEN CLC Genomics Workbench
QIAGEN CLC Genomics Workbench
For analyzing, comparing, and visualizing next-generation sequencing data
QIAGEN Clinical Insight (QCI) Analyze
QIAGEN Clinical Insight (QCI) Analyze
The bioinformatic complement to the GeneReader NGS System
GeneRead Sequencing Q Kits
GeneRead Sequencing Q Kits
For preparation of DNA for next-generation sequencing (NGS) applications using the QIAGEN GeneReader instrument
GeneRead QIAact Actionable Insights Tumor Panel
GeneRead QIAact Actionable Insights Tumor Panel
For actionable tumor insights from FFPE and liquid biopsy samples
QIAseq Tumor Mutational Burden Panels
QIAseq Tumor Mutational Burden Panels
For creating a comprehensive profile of Tumor Mutational Burden (TMB) and Microsatellite Instability Status (MSI)
QIAseq Targeted RNAscan Custom Panel
QIAseq Targeted RNAscan Custom Panel
Applying digital RNA sequencing to scan for known and novel fusion genes
GeneRead DNAseq Panel PCR Kit V2
GeneRead DNAseq Panel PCR Kit V2
For targeted enrichment prior to NGS using GeneRead DNAseq Panels V2
GeneRead QIAact BRCA Advanced DNA UMI Panel
GeneRead QIAact BRCA Advanced DNA UMI Panel
For detection of somatic variants from FFPE samples and pathogenic germline variants from blood
REPLI-G Kits
REPLI-G Kits
For highly uniform whole genome amplification from 10ng of genomic DNA
GeneRead Clonal Amp Q Kit
GeneRead Clonal Amp Q Kit
For clonal amplification of DNA libraries for next-generation sequencing (NGS) applications using the QIAGEN GeneRead QIAcube instrument
GeneRead DNA Library l Core Kit
GeneRead DNA Library l Core Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq Human Exome Kits
QIAseq Human Exome Kits
Reduce exome sequencing costs by up to 50%, improve scalability with a single-day, automation-compatible sample to sequencing workflow and accelerate time to insights
QIAseq UPX 3’ Transcriptome Kits
QIAseq UPX 3’ Transcriptome Kits
For high-throughput 3' transcriptome analysis from up to 10 ng of purified RNA, cell lysates and single cells using next-generation sequencing
REPLI-g Advanced DNA Single Cell Kit
REPLI-g Advanced DNA Single Cell Kit
For whole genome amplification (WGA) from single eukaryotic cells, limited samples or purified genomic DNA
QIAseq 1-Step Amplicon Library Kit
QIAseq 1-Step Amplicon Library Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq Ultralow Input Library Kit
QIAseq Ultralow Input Library Kit
Highly flexible DNA library preparation for sequencing with Illumina instruments
REPLI-g WTA Single Cell Kit
REPLI-g WTA Single Cell Kit
For whole transcriptome amplification of total RNA or mRNA from single cells
GeneRead DNA Library Q Kit
GeneRead DNA Library Q Kit
Automated and streamlined to save time
QIAseq UPX 3’ Targeted RNA Panels
QIAseq UPX 3’ Targeted RNA Panels
For ultraplex (UPX) gene expression analysis using 3' RNA-seq from single cells and low-input samples
QIAact Myeloid DNA UMI Panel
QIAact Myeloid DNA UMI Panel
For detection of key mutations in myeloid malignancies from blood and bone marrow
OmicSoft Studio on the Cloud
OmicSoft Studio on the Cloud
Leveraging state of the art NGS and OMIC data analysis in the cloud
QIAseq Immune Repertoire RNA Library Kits
QIAseq Immune Repertoire RNA Library Kits
For human and mouse immune repertoire screening
GeneRead DNA I Amp Kit
GeneRead DNA I Amp Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq Targeted RNA Panels and Indices
QIAseq Targeted RNA Panels and Indices
For highly accurate gene expression quantification using UMIs
REPLI-g Cell WGA & WTA Kit
REPLI-g Cell WGA & WTA Kit
For parallel whole genome and whole transcriptome amplification from cells and limited samples
QIAseq Targeted RNAscan Panels
QIAseq Targeted RNAscan Panels
Applying digital RNA sequencing to scan for known and novel fusion genes
QIAseq FX Single Cell RNA Library Kit
QIAseq FX Single Cell RNA Library Kit
Single cell RNA-seq libraries that provide a deeper view of the transcriptome
QIAseq Library Quant System
QIAseq Library Quant System
For qPCR-enabled quantification of NGS libraries
QIAseq Targeted RNA Panels
QIAseq Targeted RNA Panels
Digital RNAseq for gene expression profiling
QIAseq 16S/ITS Region Panels
QIAseq 16S/ITS Region Panels
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
QIAseq Targeted DNA Booster Panels
QIAseq Targeted DNA Booster Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq FX Single Cell DNA Library Kit
QIAseq FX Single Cell DNA Library Kit
Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
REPLI-g FFPE Kit
REPLI-g FFPE Kit
For direct whole genome amplification of DNA from formalin-fixed, paraffin-embedded (FFPE) tissue
QIAGEN CLC Workbench Modules
QIAGEN CLC Workbench Modules
For enhancing functionalities of CLC Main Workbench, CLC Genomics Workbench, CLC Genomics Workbench Premium and CLC Server solutions
REPLI-g Mitochondrial DNA Kit
REPLI-g Mitochondrial DNA Kit
For highly uniform whole genome amplification from human and non-human mitochondrial DNA
GeneRead Size Selection Kit
GeneRead Size Selection Kit
For quick and reliable removal of DNA fragments <150 bp for library preparation in NGS applications
QIAseq DNA QuantiMIZE Kits
QIAseq DNA QuantiMIZE Kits
For quantification and qualification of amplifiable DNA prior to NGS
QIAseq Targeted DNA Extended Panels
QIAseq Targeted DNA Extended Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq Multimodal Panels
QIAseq Multimodal Panels
A single day sample to sequencing workflow for simultaneous enrichment and profiling of DNA variants, RNA fusions and gene expression levels from one sample input, as low as 10 ng
QIAseq miRNA Library QC PCR Panel and Assays
QIAseq miRNA Library QC PCR Panel and Assays
For evaluating RNA sample quality prior to miRNA/small RNA NGS library preparation and for assessing NGS performance post-sequencing
QIAseq Pan-cancer Multimodal Panel
QIAseq Pan-cancer Multimodal Panel
The only one-day, low-input sample to sequencing workflow for simultaneous and comprehensive genomic profiling of DNA variants, RNA fusions and assessing TMB/MSI in solid tumors and heme malignancies
QIAseq Methyl Library Kit
QIAseq Methyl Library Kit
For robust library preparation for DNA methylation analysis
QIAseq Targeted Methyl Custom Panels
QIAseq Targeted Methyl Custom Panels
A liquid biopsy-compatible solution for targeting methylation status of DNA, from as low as 1 ng input DNA from cells and tissues, or 10 ng from FFPE samples and liquid biopsies
QIAseq Targeted Methyl Panels
QIAseq Targeted Methyl Panels
A liquid biopsy-compatible solution for targeting methylation status of DNA, from as low as 1 ng input DNA from cells and tissues, or 10 ng from FFPE samples and liquid biopsies
QIAGEN CLC Genomics Cloud Engine
QIAGEN CLC Genomics Cloud Engine
For bringing CLC tools to private AWS accounts
QIAGEN CLC Genomics Server
QIAGEN CLC Genomics Server
For flexible next-generation sequencing data analysis
QIAGEN CLC Main Workbench
QIAGEN CLC Main Workbench
For advanced DNA, RNA, and protein analyses
GeneRead Databank
GeneRead Databank
For automated archiving of GeneReader run data
GeneRead Link Software
GeneRead Link Software
For automated data transfer between the GeneReader NGS System and LIMS
GeneRead QIAact Custom Panels
GeneRead QIAact Custom Panels
For targeted sequencing of the variants most relevant to your research
QIAGEN Ingenuity Pathway Analysis (IPA)
QIAGEN Ingenuity Pathway Analysis (IPA)
For modeling, analyzing, and understanding complex 'omics data
OmicSoft Concurrent Licenses
OmicSoft Concurrent Licenses
State of the art bioinformatics: statistics, visualization and analysis
QIAact Lung Plasma Track Panel
QIAact Lung Plasma Track Panel
For detecting lung cancer mutations in ccfDNA with analytical sensitivity down to 0.1% variant allele frequency
QIAGEN CLC Genomics Workbench Premium
QIAGEN CLC Genomics Workbench Premium
For single cell analysis, microbial profiling, pathogen typing and outbreak analysis using state-of-the-art bioinformatics
QIAseq SARS-CoV-2 Primer Panel
QIAseq SARS-CoV-2 Primer Panel
For targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection

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