DNA 测序
自信地检测低频突变
在数字 DNA 测序 (DNA-seq) 应用中，要想获得可靠的结果，前提条件是覆盖范围均匀，并能处理大量数据和分析产生的大量突变。应对这些挑战需要在测序和生物信息学基础设施和能力两方面进行大量投资。此外，与其他方法（全外显子组、靶向 panel ）相比，所获得的可指导用药数据可能并不足以显著到能够证明成本增加的合理性。
我们用于靶向数字 DNA 测序的专用 DNA 测序试剂盒让您能够自信地检测低频突变。对于合并靶向 DNA 和 RNA 测序，我们提供multimodal产品，以精简您的工作流程，并实现 DNA 变异、RNA 融合和基因表达水平的富集和图谱分析。
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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 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
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
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 Multimodal Pan-Cancer 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 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
QIAseq UPX Single Cell DNA Lib Kit
For ultraplex pooling of Repli-g amplified samples starting from 1 cell or 1 ng of total DNA
QIAseq Targeted cfDNA Ultra Panels
For ultrasensitive targeted next-generation sequencing of cfDNA on Illumina platforms