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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
QIAseq Multimodal HT Custom Panels
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
QIAxcel Connect System
Effortless, cost-effective, high-resolution DNA or RNA gel electrophoresis – all in a single instrument
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
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
REPLI-G Kits
REPLI-G Kits
For highly uniform whole genome amplification from 10ng of genomic DNA
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 or cell lysates using next-generation sequencing

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