Building confidence in the results of Liquid Biopsies – authentic cfDNA reference samples for an improved quality assurance
Our advanced liquid biopsy platform combines digital PCR (dPCR/ddPCR) and next-generation sequencing (NGS) technologies to achieve ultra-sensitive ctDNA detection. Rigorous quality control protocols minimize false positives/negatives, ensuring clinical-grade accuracy for informed treatment decisions and research reproducibility.
Clinically validated RMs address critical preanalytical variables including DNA extraction efficiency optimization Precise concentration quantification Fragment size distribution analysis SNV detection across VAF ranges (0.01%-5%) These standardized controls reduce inter-lab variability in ctDNA analysis, ensuring comparable results across clinical trials and diagnostic settings while enhancing treatment response monitoring and prognostic accuracy.
Reference Materials (RMs) derived from cancer cell lines enable precise benchmarking of ctDNA detection methods. These characterized controls facilitate assay validation, sensitivity optimization (down to 0.1% VAF), and systematic bias identification, essential for translating research findings into clinical applications while maintaining reproducibility across laboratories.
Driving Oncology Innovation Through Reliable Detection
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