Liquid Biopsy

Uncover the full discovery potential of liquid biopsy

Using a simple blood sample, free-floating nucleic acids or nucleic acids from circulating cells and exosomes can reveal valuable insights into genomic drivers of cancer development or chromosome aneuploidies in fetal development research. This genomic analysis of peripheral blood, known as a “liquid biopsy”, presents a low-cost, low-risk way to access valuable genomic information without invasive surgical procedures. QIAseq NGS products enable you to uncover the full discovery potential from any liquid biopsy sample. ...

Smooth integration with QIAGEN sample extraction technologies to maximize sample carry-over to NGS workflow
High adapter ligation efficiencies to maximize library yields
Even representation of the genome for in-depth genomic analysis – even from single cells
Specific target-enrichment of cancer-related genes
Sensitive detection of relevant mutations down to 1% allelic frequency

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		QIAseq cfDNA All-in-One Kits For conversion of cfDNA from plasma to NGS library for any liquid biopsy samples Show details	See products
		QIAseq FX Single Cell DNA Library Kit Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity Show details	See products
		QIAseq Ultralow Input Library Kit For preparation of DNA libraries for next-generation sequencing (NGS) applications that use Illumina® instruments Show details	See products
		QIAseq FX Single Cell RNA Library Kit Single cell RNA-seq libraries that provide a deeper view of the transcriptome Show details	See products
		QIAseq Targeted RNA Panels Digital RNAseq for gene expression profiling Show details	See products
		QIAseq 1-Step Amplicon Library Kit For fast and efficient preparation of DNA libraries for use in NGS applications Show details	See products
		QIAseq Targeted DNA Panels Digital DNA sequencing to confidently detect low-frequency variants Show details	See products