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NuProbe | Improving analytical sensitivity in DNA biomarkers At NuProbe, we are developing innovative assays to accelerate cancer research Our products allow laboratories to detect and quantify low-abundant variants across multiple platforms from both cell-free DNA and tissue specimens
NuProbe | Fierce Pharma NuProbe is a cutting-edge genomics and molecular diagnostics company with revolutionary molecular diagnostic technologies to improve the sensitivity of sequencing mutations and copy number
NuProbe - Crunchbase Company Profile Funding NuProbe is a cutting-edge genomics and molecular diagnostics company A PCR-based rare allele enrichment method that selectively amplifies low-frequency DNA variants down to 0 01% variant allele frequency (VAF)
NuProbe NuProbe has proprietary technology to reduce costs and enhance the sensitivity of next-generation sequencing (NGS) and qPCR assays by pioneering ultrasensitive and highly-multiplexed assays
Nuprobe | Science Company | Labroots Founded in 2016 and building on scientific findings licensed from the Wyss Institute at Harvard and Rice University, NuProbe is a privately held company with facilities in the US (Houston, TX) and China (Shanghai)
NuProbe Company Profile - Office Locations, Competitors . . . - Craft NuProbe is a company developing technologies in genomics for disease detection It develops a PCR-based (polymerase chain reaction) enrichment method called blocker displacement amplification for selective amplification of low abundant sequence variants in a background of wildtype DNA
Nuprobe Closes $11 Million Series A Round to Develop Molecular . . . Developed at and licensed from Harvard University’s Wyss Institute for Biologically Inspired Engineering and Rice University, NuProbe’s toehold probe-based technology is a breakthrough molecular strategy to test for diverse disease signatures, including cancer
NuProbe - Fierce Biotech NuProbe is a cutting-edge genomics and molecular diagnostics company with revolutionary molecular diagnostic technologies to improve the sensitivity of sequencing mutations and copy number