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.
QIAseq Targeted DNA Pro PanelsCataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
QIAseq Targeted DNA Pro Custom PanelsCustom targeted panel for detecting low-frequency variants by digital DNA sequencing
QIAseq Targeted cfDNA Ultra PanelsCataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
QIAseq cfDNA All-in-One KitsFor conversion of cfDNA from plasma to NGS library for any liquid biopsy samples
QIAseq FX DNA Library KitAll-enzymatic whole genome and hybrid capture library preparation for Illumina instruments with minimal bias
QIAseq Human Exome KitReduce exome sequencing costs by up to 50%, improve scalability with a single-day, automation-compatible sample to sequencing workflow
QIAseq Ultralow Input Library KitHighly flexible DNA library preparation for sequencing with Illumina instruments
QIAseq 16S/ITS Screening Panels and Index KitsFor next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
QIAseq 16S/ITS Region PanelsFor next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
QIAseq xHyb Viral and Bacterial PanelsFor high-quality targeted viral and bacterial sequencing using hybrid capture
QIAseq xHyb Mycobacterium Tuberculosis PanelFor the culture-free Whole Genome Enrichment of Mycobacterium tuberculosis
QIAseq 1-Step Amplicon Library KitFor fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq xHyb Long Read PanelsFor high-quality targeted viral and bacterial sequencing using hybrid capture
QIAseq Targeted DNA Booster PanelsSpike-in pools to either boost coverage or augment targets across specific regions of any panel
QIAseq Targeted DNA PanelsCataloged targeted panels for detecting low-frequency variants by digital DNA sequencing
Custom targeted panel for detecting low-frequency variants by digital DNA sequencing
QIAseq Multimodal Custom PanelsA 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 Multimodal PanelsA 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 Multimodal DNA/RNA Library KitsFor simultaneous whole genome sequencing and whole transcriptome sequencing library preparation from a single sample
QIAseq Targeted Methyl PanelsA 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 Targeted Methyl Custom PanelsA 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 xHYB Custom Human PanelsCustom targeted panel for detecting low-frequency variants by digital DNA sequencing