下一代测序
通过 Sample to Insight 解决方案加快 NGS 性能的提升
高通量二代测序 (Next-Generation Sequencing, NGS) 技术持续提供丰富的序列信息，从而在广泛的研究领域取得重大进展和新发现。为了增强您基于 NGS 的特定研究并帮助您实现目标，我们提供专用的 NGS 靶标富集、文库制备和单细胞解决方案，以消除偏差并实现均匀覆盖。我们简化的实验方案易于使用，并可将无缝整合的工作流程进行自动化，充分发挥二代测序技术的威力。我们共同努力，让改善生活成为可能。
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QIAxcel DNA Kit
用于使用 QIAxcel 仪器自动分析 DNA 片段
QIAxcel Connect System
Effortless, cost-effective, high-resolution DNA or RNA gel electrophoresis – all in a single instrument
QIAseq Targeted DNA Pro Custom Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing.
QIAseq RNA Fusion XP Custom Panel
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
QIAseq RNA Fusion XP Panels
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
QIAseq FastSelect RNA Library Kits
For stranded RNA-seq library construction for complete transcriptome coverage in less than 5 hours
QIAseq DIRECT SARS-CoV-2 Kits
For fast, targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection
REPLI-G Kits
For highly uniform whole genome amplification from 10ng of genomic DNA
QIAseq Targeted DNA Pro Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing
QIAseq xHYB Viral and Bacterial Panels
For targeted viral and bacterial sequencing using hybrid capture
QIAseq Beads
For DNA purification with NGS library size selection
QIAseq FastSelect Epidemiology Kits
For rapid rRNA removal for RNA-seq library preparation from human, mouse, rat and bacteria samples
QIAseq UPXome RNA Library Kits
RNA-seq library construction for low-input samples using ultraplex (UPX) cDNA pooling workflows for complete transcriptome or 3’ RNA-seq starting with total RNA or enriched mRNA
QIAseq Targeted RNA-seq Panel for T-cell Receptor
For RNA-seq library construction of T-cell receptor (TCR) alpha, beta, gamma and delta genes using 200 pg to 1000 ng of RNA from human or mouse samples.
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 xHYB Custom Human Panels
Customizable genome-wide content for a single-day, automation-compatible sample-to-sequencing workflow that accelerates time to insights
QIAseq Targeted RNA Custom Panels and Indices
For highly accurate gene expression quantification using UMIs
QIAseq Multimodal DNA/RNA Library Kit
For simultaneous whole genome sequencing and whole transcriptome sequencing library preparation from a single sample
QIAseq Normalizer Kits
For efficient and reproducible NGS library normalization
QIAseq FastSelect Custom RNA Removal Kits
For rapid removal of unwanted RNAs during RNA-seq library preparation
QIAseq FastSelect –rRNA Fly Kits
For rapid rRNA removal for RNA-seq library preparation from Drosophila melanogaster (fly) samples
QIAseq Single Cell DNA Library Kits UDI
For PCR-free, single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
QIAseq Single Cell RNA Library Kits UDI
For single-cell RNA-seq libraries that provide a deeper view of the transcriptome
QIAseq xHYB CGP Panels
For comprehensive genomic profiling of DNA and RNA variants from a single nucleic acid sample
QIAseq Targeted cfDNA Ultra Panels
For ultrasensitive targeted next-generation sequencing of cfDNA on Illumina platforms
Human Somatic Mutation Database
Access to real-world data and two decades of expert curation
QIAseq FastSelect –rRNA Fish Kits
For rapid rRNA removal for RNA-seq library preparation from fish total RNA samples
QIAseq FastSelect –rRNA Worm Kits
For rapid rRNA removal for RNA-seq library preparation from Caenorhabditis elegans (worm) samples
QIAseq 16S/ITS Screening Panels and Index Kits
For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal communities
QIAseq xHYB Long Read Panels
For highly accurate and comprehensive analysis of complex genomic regions using long-read sequencing
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 xHYB Mycobacterium tuberculosis Panel
For the culture-free Whole Genome Enrichment of Mycobacterium tuberculosis
QIAGEN Biomedical Knowledge Bases
Leading biomedical relationships knowledge to drive innovation, confidently and efficiently
COSMIC
Catalogue of Somatic Mutations in Cancer
GeneGlobe Analyze – NGS analysis credits
Analysis of RNA-seq data with pathway interpretation and convenient design of follow-up biomarker verification assays in GeneGlobe
GeneRead DNAseq Gene Panels V2
Digital DNA sequencing to confidently detect low-frequency variants
Related Applications and Insights
Digital is the new absolute
By partitioning samples into a large number of individual reactions, digital PCR makes it surprisingly easy to detect the single positive.
QIAGEN Digital Insights
Expert curated genomic and clinical knowledge, together with bioinformatics software and services, for actionable insights.
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