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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QIAseq xHYB Trinity workflow
For QIAseq NGS library prep and hybrid capture-based target enrichment with Element Biosciences’ AVITI platform and Trinity sequencing workflow
QIAseq Universal Metagenome Library Kit
For preparing sequencing-ready libraries from RNA, DNA or total nucleic acid and from all microbial targets viral, bacterial or fungal, in a single workflow.
QIAseq Viral Safety and Clearance
For targeted enrichment and next-generation sequencing to support viral safety evaluation of biopharmaceutical products
QIAseq xHYB HRD Panel
Comprehensive HRD panel for simultaneous assessment of genomic instability and HRR pathway
QIAseq Multimodal DNA/RNA Library Kit
For simultaneous whole genome sequencing and whole transcriptome sequencing library preparation from a single sample
QIAseq xHYB CGP Panels
For comprehensive genomic profiling of DNA and RNA variants from a single nucleic acid sample
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
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
QIAseq Multimodal 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 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
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