Next-Generation Sequencing Panels & Kits

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