
Next-generation sequencing (NGS) is driving new and exciting discoveries across applications, from single cell analysis, liquid biopsy research, circulating-free DNA (cfDNA) studies, genome wide association studies, metagenomics and targeted sequencing. Our innovative and high-quality NGS panels and kits can alleviate workflow challenges and help reveal meaningful insights from your results.
We employ a digital sequencing approach using molecular barcodes to overcome issues associated with PCR duplicates such as false positives and library bias. So, whether you’re looking to analyze copy number variation (CNV) or detect SNPs, InDels or other mutations and allelic differences, we have a DNA-seq solution that lets you detect your low-frequency variants of interest with confidence.
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 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
Indices for QIAseq Targeted NGS now available in unique dual bar-coded format
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
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 the culture-free Whole Genome Enrichment of Mycobacterium tuberculosis
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
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
Cataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
Extends the content of any cataloged panel with up to 100 additional primers
Custom targeted panel for detecting low-frequency variants by digital DNA sequencing
Dedicated QIAseq panels for human identity investigations
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
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
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
Custom targeted panel for detecting low-frequency variants by digital DNA sequencing