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.
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88 Products found
QIAseq Targeted DNA Pro Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing
QIAseq Targeted DNA Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq Targeted DNA Pro Custom Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing.
QIAseq Targeted DNA Custom Panels
Digital DNA sequencing to confidently detect low-frequency variants
COSMIC
Catalogue of Somatic Mutations in Cancer
HGMD
The gold standard resource for comprehensive data on published human inherited disease mutations.
Human Somatic Mutation Database
Access to real-world data and two decades of expert curation
REPLI-g Single Cell Kit
For highly uniform whole genome amplification (WGA) from single cells or limited sample material
QIAseq miRNA Library Kit
Gel-free miRNA Sample to Insight solution for differential expression analysis and novel discovery using next-generation sequencing
QIAGEN OmicSoft Lands
Public and private genomic data for disease research
QIAseq Index Kits
Indices for QIAseq Targeted NGS now available in unique dual bar-coded format
QIAseq FX DNA Library Kit
For all-enzymatic whole genome and hybrid capture library preparation for Illumina instruments with minimal bias
QIAseq Multimodal HT 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 Connect System
Effortless, cost-effective, high-resolution DNA or RNA gel electrophoresis – all in a single instrument
QIAxcel DNA Kits
For automated analysis of DNA fragments using QIAxcel instruments
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
For analyzing, comparing, and visualizing next-generation sequencing data
QIAGEN Clinical Insight (QCI) Analyze
The bioinformatic complement to the GeneReader NGS System
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
Applying digital RNA sequencing to scan for known and novel fusion genes
GeneRead DNAseq Panel PCR Kit V2
For targeted enrichment prior to NGS using GeneRead DNAseq Panels V2
REPLI-G Kits
For highly uniform whole genome amplification from 10ng of genomic DNA
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
For high-throughput 3' transcriptome analysis from up to 10 ng of purified RNA or cell lysates using next-generation sequencing
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
For fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq Ultralow Input Library Kit
Highly flexible DNA library preparation for sequencing with Illumina instruments
REPLI-g WTA Single Cell Kit
For whole transcriptome amplification of total RNA or mRNA from single cells
QIAseq UPX 3’ Targeted RNA Panels
For ultraplex (UPX) gene expression analysis using 3' RNA-seq from single cells and low-input samples
OmicSoft Studio on the Cloud
Leveraging state of the art NGS and OMIC data analysis in the cloud
QIAseq Immune Repertoire RNA Library Kits
For human and mouse immune repertoire screening
QIAseq Targeted RNA Custom Panels and Indices
For highly accurate gene expression quantification using UMIs
REPLI-g Cell WGA & WTA Kit
For parallel whole genome and whole transcriptome amplification from cells and limited samples
QIAseq Targeted RNAscan Panels
Applying digital RNA sequencing to scan for known and novel fusion genes
QIAseq FX Single Cell RNA Library Kit
Single cell RNA-seq libraries that provide a deeper view of the transcriptome
QIAseq Library Quant System
For qPCR-enabled quantification of NGS libraries
QIAseq Targeted RNA Panels and Indices
Digital RNAseq for gene expression profiling
QIAseq 16S/ITS Region Panels
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
QIAseq Targeted DNA Booster Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq FX Single Cell DNA Library Kit
Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
REPLI-g FFPE Kit
For direct whole genome amplification of DNA from formalin-fixed, paraffin-embedded (FFPE) tissue
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
For highly uniform whole genome amplification from human and non-human mitochondrial DNA
QIAseq DNA QuantiMIZE Kits
For quantification and qualification of amplifiable DNA prior to NGS
QIAseq Targeted DNA Extended Panels
Digital DNA sequencing to confidently detect low-frequency variants
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
For evaluating RNA sample quality prior to miRNA/small RNA NGS library preparation and for assessing NGS performance post-sequencing
QIAseq Pan-Cancer Multimodal HT 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
For robust library preparation for DNA methylation analysis
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 16S/ITS Smart Control
For use with QIAseq 16S/ITS Panels to monitor library construction steps and procedure-introduced contamination
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
For bringing CLC tools to private AWS accounts
QIAGEN CLC Genomics Server
For flexible next-generation sequencing data analysis
QIAGEN CLC Main Workbench
For advanced DNA, RNA, and protein analyses
QIAGEN Ingenuity Pathway Analysis (IPA)
For modeling, analyzing, and understanding complex 'omics data
OmicSoft Concurrent Licenses
State of the art bioinformatics: statistics, visualization and analysis
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
For targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection
QIAseq Targeted RNA Extended Panels
Digital RNAseq for gene expression profiling
QIAseq Normalizer Kits
For efficient and reproducible NGS library normalization
QIAseq Beads
For DNA purification with NGS library size selection
Microbiome WGS SeqSets
For comprehensive whole genome metagenomics with an all-in-one solution for microbiome research
QIAGEN Clinical Insight (QCI) Interpret
Expedite variant interpretation and reporting in-house for any NGS panel, exome, or genome from your sequencing platform.
QIAGEN Clinical Insight (QCI) Interpret One
Deliver oncologist-ready variant interpretation reports
QIAseq Targeted cfDNA Ultra Panels
For ultrasensitive targeted next-generation sequencing of cfDNA on Illumina platforms
GeneGlobe Analyze – NGS analysis credits
Analysis of RNA-seq data with pathway interpretation and convenient design of follow-up biomarker verification assays in GeneGlobe
QIAseq Fusion XP Custom Targeted Panels
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
QIAseq Single Cell RNA Library Kits UDI
For single-cell RNA-seq libraries that provide a deeper view of the transcriptome
QIAseq Fusion XP Targeted Panels
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
QIAseq Targeted RNA-seq Panel for T-cell Receptor
For RNA-seq library construction of T-cell receptor (TCR) alpha, beta, gamma and delta genes using 200 pg to 1000 ng of RNA from human or mouse samples.
QIAseq UPXome RNA Library Kits
RNA-seq library construction for low-input samples using ultraplex (UPX) cDNA pooling workflows for complete transcriptome or 3’ RNA-seq starting with total RNA or enriched mRNA