Next-generation sequencing can deliver unprecedented insights, unraveling the intricacies of the genome and transcriptome in biomarker research, gene expression studies, viral epidemiology and disease surveillance, as well as comprehensive genomic profiling to identify variants implicated in cancer and other diseases.
Our NGS panels and kits support a wide range of sequencing needs and scales: from differential expression analysis to variant and mutation detection, from sequencing targeted regions of interest or the entire exome, transcriptome or genome, we can help you overcome typical workflow challenges and get to your insights faster.
Cataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
Custom targeted panel for detecting low-frequency variants by digital DNA sequencing
Cataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
For creating a comprehensive profile of Tumor Mutational Burden (TMB) and Microsatellite Instability Status (MSI)
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
Indices for QIAseq Targeted NGS now available in unique dual bar-coded format
For rapid removal of unwanted RNAs during RNA-seq library preparation
For conversion of cfDNA from plasma to NGS library for any liquid biopsy samples
All-enzymatic whole genome and hybrid capture library preparation for Illumina instruments with minimal bias
Reduce exome sequencing costs by up to 50%, improve scalability with a single-day, automation-compatible sample to sequencing workflow
Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
Highly flexible DNA library preparation for sequencing with Illumina instruments
Single cell RNA-seq libraries that provide a deeper view of the transcriptome
For high-throughput 3' transcriptome analysis from up to 10 ng of purified RNA, cell lysates and single cells using next-generation sequencing
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
For use with QIAseq 16S/ITS Panels to monitor library construction steps and procedure-introduced contamination
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
For high-quality targeted viral and bacterial sequencing using hybrid capture
For fast and efficient preparation of DNA libraries for use in NGS applications
For quantification and qualification of amplifiable DNA prior to NGS
For qPCR-enabled quantification of NGS libraries
For evaluating RNA sample quality prior to miRNA/small RNA NGS library preparation and for assessing NGS performance post-sequencing
Spike-in pools to either boost coverage or augment targets across specific regions of any panel
Digital DNA sequencing to confidently detect homologous recombination repair (HRR) biomarkers
Dedicated QIAseq panels for human identity investigations
Cataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
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
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
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
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
Gel-free miRNA Sample to Insight solution for differential expression analysis and novel discovery using next-generation sequencing
Applying digital RNA sequencing to scan for known and novel fusion genes
Applying digital RNA sequencing to scan for known and novel fusion genes
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
Digital RNAseq for gene expression profiling
Digital RNAseq for gene expression profiling
For human and mouse immune repertoire screening
For ultraplex (UPX) gene expression analysis using 3' RNA-seq from single cells and low-input samples
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
For targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection
For fast, targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection