Oncology and Liquid Biopsy
Low cost and rapid turn-around measurement for MRD and tumor profiling applications
Zero dead volume and high DNA volume input (up to 30uL in a 50uL PCR reaction) maximizes usage of precious samples
Comboplex™ technology enables interrogation of a high number of mutations within the same low-cost assay
Single molecule counting greatly improves sensitivity for MRD applications
Multiplexed Pathogen Detection and Quantitation
Universal Multiplex™ and Comboplex technologies enable both small-scale (2-4 targets) and large-scale (20+) multiplex strategies to rapidly identify and quantify pathogens
High dynamic range paired with single molecule counting for accurate quantitation of viral load
Go beyond mere presence and absence measurement with precise quantitation of each pathogen
Cell and Gene Therapy
Low cost and quick multiplex assay design using Universal Multiplex™ technology without the need for hydrolysis probes
High dynamic range with single molecule precision for capturing a wide range of sample types from viral titer measurement to gene therapy development QC assays
Comboplex™ technology enables interrogation of dozens of gene therapy targets and viral backbone within the same assay
Gene Expression Analysis
6-log dynamic range with single molecule precision allows for unprecedented digital PCR ability to capture gene expression dynamics across broad range of biological variation
Universal Multiplex™ technology empowers users to rapidly and cost-effectively design flexible gene expression panels
Comboplex™ technology enables high-order multiplexing for RNA-seq biomarker validation studies
Human ID
Comboplex™ technology enables interrogation of high number of gene targets and SNPs within the same assay
Precise counting of alleles enables applications with mixed human samples such as in areas of forensics, organ transplant, and pregnancies
Noninvasive prenatal testing (NIPT)
Precision counting makes UltraPCR the first practical platform for PCR-based NIPT application
Rapid turn-around, low cost, with a simple workflow, as compared to NGS readout
Zero dead volume and high DNA volume input maximizes molecule quantification to enable precise detection of aneuploidy events
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