DNA Sequencing
Confidently detect low-frequency variants
Uniform coverage and being able to deal with the large amounts of data and high number of variants that result from the analysis are prerequisites for reliable results in your digital DNA sequencing (DNA-seq) applications. Addressing these challenges requires a steep investment both in sequencing and bioinformatics infrastructure and capabilities. Additionally, actionable data gained relative to alternative methods (whole exome, targeted panels) may not be significant enough to justify the increased cost.
Our dedicated DNA sequencing kits for targeted digital DNA sequencing enable you to confidently detect low-frequency variants. For consolidated targeted DNA and RNA sequencing, we provide multimodal products to streamline your workflow and enable enrichment and profiling of DNA variants, RNA fusions and gene expression levels.
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QIAseq Targeted DNA Pro Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing
QIAseq Targeted DNA Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq Targeted DNA Pro Custom Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing.
GeneRead DNAseq Gene Panels V2
Digital DNA sequencing to confidently detect low-frequency variants
REPLI-g Single Cell Kit
对单个细胞或有限的样本进行高度均一的全基因组扩增（WGA）
QIAseq Targeted RNA Indexes
用于对目标RNA测序所需样本和对QIAseq Targeted RNA Panels生成的RNA文库测序进行索引
QIAseq FX DNA Library Kit
For all-enzymatic whole genome and hybrid capture library preparation for Illumina instruments with minimal bias
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
QIAseq Tumor Mutational Burden Panels
For creating a comprehensive profile of Tumor Mutational Burden (TMB) and Microsatellite Instability Status (MSI)
REPLI-G Kits
For highly uniform whole genome amplification from 10ng of genomic DNA
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 1-Step Amplicon Library Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq Ultralow Input Library Kit
Highly flexible DNA library preparation for sequencing with Illumina instruments
REPLI-g Cell WGA & WTA Kit
从细胞和有限的样本中同时扩增全基因组和全转录组
QIAseq Targeted DNA Booster Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq FX Single Cell DNA Library Kit
Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
REPLI-g FFPE Kit
直接对福尔马林固定、石蜡包埋组织（FFPE）中的DNA进行全基因组扩增
REPLI-g Mitochondrial DNA Kit
对人类线粒体DNA进行高度均一的全基因组扩增
QIAseq Targeted DNA Extended Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq Pan-Cancer Multimodal HT Panel
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
QIAseq Targeted Methyl Custom Panels
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
QIAseq Targeted Methyl Panels
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
QIAseq Targeted cfDNA Ultra Panels
For ultrasensitive targeted next-generation sequencing of cfDNA on Illumina platforms
QIAseq xHYB Human Hybrid Capture Panels
Curated genome-wide content for a single-day, automation-compatible sample to sequencing workflow that accelerates time to insights
QIAseq Single Cell DNA Library Kits UDI
For PCR-free, single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
QIAseq xHYB Custom Human Panels
Customizable genome-wide content for a single-day, automation-compatible sample-to-sequencing workflow that accelerates time to insights
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